← Back to variant description
GeneBe API Showcase
This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.
API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.
Documentation & Advanced Usage
• Complete API documentation:docs.genebe.net/docs/api/overview/
• Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/
• Python client for pandas:pypi.org/project/genebe/
• Java CLI for VCF files:github.com/pstawinski/genebe-cli
• All tools documented at:docs.genebe.net
API Request Examples for Variant: 3-71198319-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=71198319&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "3",
"pos": 71198319,
"ref": "G",
"alt": "C",
"effect": "synonymous_variant",
"transcript": "NM_001244810.2",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "NM_001349338.3",
"protein_id": "NP_001336267.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 667,
"cdna_end": null,
"cdna_length": 7177,
"mane_select": "ENST00000649528.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001349338.3"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000649528.3",
"protein_id": "ENSP00000497369.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 667,
"cdna_end": null,
"cdna_length": 7177,
"mane_select": "NM_001349338.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000649528.3"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000318789.11",
"protein_id": "ENSP00000318902.5",
"transcript_support_level": 1,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 578,
"cdna_end": null,
"cdna_length": 7103,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000318789.11"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ENSG00000285708",
"gene_hgnc_id": null,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000647725.1",
"protein_id": "ENSP00000497585.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 1036,
"cdna_end": null,
"cdna_length": 3028,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000647725.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000318779.7",
"protein_id": "ENSP00000318721.3",
"transcript_support_level": 1,
"aa_start": 21,
"aa_end": null,
"aa_length": 114,
"cds_start": 63,
"cds_end": null,
"cds_length": 345,
"cdna_start": 539,
"cdna_end": null,
"cdna_length": 843,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000318779.7"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000471386.3",
"protein_id": "ENSP00000497992.1",
"transcript_support_level": 1,
"aa_start": 21,
"aa_end": null,
"aa_length": 34,
"cds_start": 63,
"cds_end": null,
"cds_length": 107,
"cdna_start": 529,
"cdna_end": null,
"cdna_length": 573,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000471386.3"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866065.1",
"protein_id": "ENSP00000536124.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 718,
"cds_start": 63,
"cds_end": null,
"cds_length": 2157,
"cdna_start": 640,
"cdna_end": null,
"cdna_length": 2790,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866065.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "NM_001244810.2",
"protein_id": "NP_001231739.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 693,
"cds_start": 63,
"cds_end": null,
"cds_length": 2082,
"cdna_start": 578,
"cdna_end": null,
"cdna_length": 7136,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001244810.2"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000648426.1",
"protein_id": "ENSP00000498110.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 693,
"cds_start": 63,
"cds_end": null,
"cds_length": 2082,
"cdna_start": 74,
"cdna_end": null,
"cdna_length": 2149,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000648426.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000923827.1",
"protein_id": "ENSP00000593886.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 692,
"cds_start": 63,
"cds_end": null,
"cds_length": 2079,
"cdna_start": 755,
"cdna_end": null,
"cdna_length": 2826,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000923827.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000923829.1",
"protein_id": "ENSP00000593888.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 692,
"cds_start": 63,
"cds_end": null,
"cds_length": 2079,
"cdna_start": 298,
"cdna_end": null,
"cdna_length": 2370,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000923829.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "NM_001244814.3",
"protein_id": "NP_001231743.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 298,
"cdna_end": null,
"cdna_length": 6808,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001244814.3"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "NM_001244816.2",
"protein_id": "NP_001231745.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 494,
"cdna_end": null,
"cdna_length": 7004,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001244816.2"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "NM_001349340.3",
"protein_id": "NP_001336269.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 572,
"cdna_end": null,
"cdna_length": 7082,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001349340.3"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "NM_032682.6",
"protein_id": "NP_116071.2",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 578,
"cdna_end": null,
"cdna_length": 7088,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_032682.6"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000498215.7",
"protein_id": "ENSP00000418102.1",
"transcript_support_level": 2,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 402,
"cdna_end": null,
"cdna_length": 2412,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000498215.7"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000648380.1",
"protein_id": "ENSP00000497344.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 491,
"cdna_end": null,
"cdna_length": 2472,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000648380.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000649631.1",
"protein_id": "ENSP00000496990.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 527,
"cdna_end": null,
"cdna_length": 2514,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000649631.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000650068.2",
"protein_id": "ENSP00000497454.2",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 535,
"cdna_end": null,
"cdna_length": 2506,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000650068.2"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866055.1",
"protein_id": "ENSP00000536114.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 703,
"cdna_end": null,
"cdna_length": 2730,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866055.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866061.1",
"protein_id": "ENSP00000536120.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 755,
"cdna_end": null,
"cdna_length": 2782,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866061.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866062.1",
"protein_id": "ENSP00000536121.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 783,
"cdna_end": null,
"cdna_length": 2810,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866062.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866063.1",
"protein_id": "ENSP00000536122.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 779,
"cdna_end": null,
"cdna_length": 2806,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866063.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866064.1",
"protein_id": "ENSP00000536123.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 590,
"cdna_end": null,
"cdna_length": 2617,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866064.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866068.1",
"protein_id": "ENSP00000536127.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 916,
"cdna_end": null,
"cdna_length": 2943,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866068.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866071.1",
"protein_id": "ENSP00000536130.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 673,
"cdna_end": null,
"cdna_length": 2700,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866071.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866073.1",
"protein_id": "ENSP00000536132.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 723,
"cdna_end": null,
"cdna_length": 2730,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866073.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866075.1",
"protein_id": "ENSP00000536134.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 581,
"cdna_end": null,
"cdna_length": 2608,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866075.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866076.1",
"protein_id": "ENSP00000536135.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 477,
"cdna_end": null,
"cdna_length": 2504,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866076.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866077.1",
"protein_id": "ENSP00000536136.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 859,
"cdna_end": null,
"cdna_length": 2886,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866077.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866080.1",
"protein_id": "ENSP00000536139.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 723,
"cdna_end": null,
"cdna_length": 2750,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866080.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866081.1",
"protein_id": "ENSP00000536140.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 738,
"cdna_end": null,
"cdna_length": 2765,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866081.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866084.1",
"protein_id": "ENSP00000536143.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 267,
"cdna_end": null,
"cdna_length": 2294,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866084.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866086.1",
"protein_id": "ENSP00000536145.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 204,
"cdna_end": null,
"cdna_length": 2231,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866086.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866087.1",
"protein_id": "ENSP00000536146.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 298,
"cdna_end": null,
"cdna_length": 2325,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866087.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866088.1",
"protein_id": "ENSP00000536147.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 245,
"cdna_end": null,
"cdna_length": 2272,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866088.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866092.1",
"protein_id": "ENSP00000536151.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 442,
"cdna_end": null,
"cdna_length": 2469,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866092.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866095.1",
"protein_id": "ENSP00000536154.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 250,
"cdna_end": null,
"cdna_length": 2277,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866095.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866097.1",
"protein_id": "ENSP00000536156.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 358,
"cdna_end": null,
"cdna_length": 2385,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866097.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866098.1",
"protein_id": "ENSP00000536157.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 168,
"cdna_end": null,
"cdna_length": 2175,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866098.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866100.1",
"protein_id": "ENSP00000536159.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 215,
"cdna_end": null,
"cdna_length": 2242,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866100.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866102.1",
"protein_id": "ENSP00000536161.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 169,
"cdna_end": null,
"cdna_length": 2176,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866102.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968296.1",
"protein_id": "ENSP00000638355.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 443,
"cdna_end": null,
"cdna_length": 2448,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968296.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968299.1",
"protein_id": "ENSP00000638358.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 823,
"cdna_end": null,
"cdna_length": 2850,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968299.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968304.1",
"protein_id": "ENSP00000638363.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 660,
"cdna_end": null,
"cdna_length": 2687,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968304.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968309.1",
"protein_id": "ENSP00000638368.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 469,
"cdna_end": null,
"cdna_length": 2475,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968309.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968310.1",
"protein_id": "ENSP00000638369.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 677,
"cds_start": 63,
"cds_end": null,
"cds_length": 2034,
"cdna_start": 314,
"cdna_end": null,
"cdna_length": 2311,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968310.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "NM_001244808.3",
"protein_id": "NP_001231737.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 667,
"cdna_end": null,
"cdna_length": 7174,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001244808.3"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "NM_001349341.3",
"protein_id": "NP_001336270.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 667,
"cdna_end": null,
"cdna_length": 7174,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001349341.3"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000493089.7",
"protein_id": "ENSP00000418524.1",
"transcript_support_level": 2,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 695,
"cdna_end": null,
"cdna_length": 3771,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000493089.7"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000648710.2",
"protein_id": "ENSP00000497430.2",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 660,
"cdna_end": null,
"cdna_length": 3074,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000648710.2"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000648718.1",
"protein_id": "ENSP00000496810.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 758,
"cdna_end": null,
"cdna_length": 2742,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000648718.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000649610.2",
"protein_id": "ENSP00000497693.2",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 667,
"cdna_end": null,
"cdna_length": 2657,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000649610.2"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866058.1",
"protein_id": "ENSP00000536117.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 809,
"cdna_end": null,
"cdna_length": 2833,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866058.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866060.1",
"protein_id": "ENSP00000536119.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 811,
"cdna_end": null,
"cdna_length": 2835,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866060.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866066.1",
"protein_id": "ENSP00000536125.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 827,
"cdna_end": null,
"cdna_length": 2851,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866066.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866067.1",
"protein_id": "ENSP00000536126.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 734,
"cdna_end": null,
"cdna_length": 2758,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866067.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866078.1",
"protein_id": "ENSP00000536137.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 601,
"cdna_end": null,
"cdna_length": 2625,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866078.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866079.1",
"protein_id": "ENSP00000536138.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 796,
"cdna_end": null,
"cdna_length": 2820,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866079.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866090.1",
"protein_id": "ENSP00000536149.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 822,
"cdna_end": null,
"cdna_length": 2846,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866090.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866091.1",
"protein_id": "ENSP00000536150.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 227,
"cdna_end": null,
"cdna_length": 2251,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866091.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866094.1",
"protein_id": "ENSP00000536153.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 288,
"cdna_end": null,
"cdna_length": 2312,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866094.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866096.1",
"protein_id": "ENSP00000536155.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 383,
"cdna_end": null,
"cdna_length": 2407,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866096.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866099.1",
"protein_id": "ENSP00000536158.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 224,
"cdna_end": null,
"cdna_length": 2248,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866099.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968297.1",
"protein_id": "ENSP00000638356.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 555,
"cdna_end": null,
"cdna_length": 2557,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968297.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968298.1",
"protein_id": "ENSP00000638357.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 570,
"cdna_end": null,
"cdna_length": 2574,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968298.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968300.1",
"protein_id": "ENSP00000638359.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 584,
"cdna_end": null,
"cdna_length": 2588,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968300.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968302.1",
"protein_id": "ENSP00000638361.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 638,
"cdna_end": null,
"cdna_length": 2662,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968302.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968303.1",
"protein_id": "ENSP00000638362.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 566,
"cdna_end": null,
"cdna_length": 2562,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968303.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968305.1",
"protein_id": "ENSP00000638364.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 676,
"cds_start": 63,
"cds_end": null,
"cds_length": 2031,
"cdna_start": 833,
"cdna_end": null,
"cdna_length": 2837,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968305.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000649596.1",
"protein_id": "ENSP00000496932.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 675,
"cds_start": 63,
"cds_end": null,
"cds_length": 2028,
"cdna_start": 538,
"cdna_end": null,
"cdna_length": 2971,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000649596.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866072.1",
"protein_id": "ENSP00000536131.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 675,
"cds_start": 63,
"cds_end": null,
"cds_length": 2028,
"cdna_start": 724,
"cdna_end": null,
"cdna_length": 2745,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866072.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866083.1",
"protein_id": "ENSP00000536142.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 675,
"cds_start": 63,
"cds_end": null,
"cds_length": 2028,
"cdna_start": 449,
"cdna_end": null,
"cdna_length": 2470,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866083.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866085.1",
"protein_id": "ENSP00000536144.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 675,
"cds_start": 63,
"cds_end": null,
"cds_length": 2028,
"cdna_start": 251,
"cdna_end": null,
"cdna_length": 2272,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866085.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866089.1",
"protein_id": "ENSP00000536148.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 675,
"cds_start": 63,
"cds_end": null,
"cds_length": 2028,
"cdna_start": 397,
"cdna_end": null,
"cdna_length": 2418,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866089.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866093.1",
"protein_id": "ENSP00000536152.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 675,
"cds_start": 63,
"cds_end": null,
"cds_length": 2028,
"cdna_start": 143,
"cdna_end": null,
"cdna_length": 2164,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866093.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968301.1",
"protein_id": "ENSP00000638360.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 675,
"cds_start": 63,
"cds_end": null,
"cds_length": 2028,
"cdna_start": 566,
"cdna_end": null,
"cdna_length": 2563,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968301.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968312.1",
"protein_id": "ENSP00000638371.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 675,
"cds_start": 63,
"cds_end": null,
"cds_length": 2028,
"cdna_start": 705,
"cdna_end": null,
"cdna_length": 3112,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968312.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968316.1",
"protein_id": "ENSP00000638375.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 675,
"cds_start": 63,
"cds_end": null,
"cds_length": 2028,
"cdna_start": 237,
"cdna_end": null,
"cdna_length": 2238,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968316.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866056.1",
"protein_id": "ENSP00000536115.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 642,
"cds_start": 63,
"cds_end": null,
"cds_length": 1929,
"cdna_start": 667,
"cdna_end": null,
"cdna_length": 2589,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866056.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866059.1",
"protein_id": "ENSP00000536118.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 642,
"cds_start": 63,
"cds_end": null,
"cds_length": 1929,
"cdna_start": 662,
"cdna_end": null,
"cdna_length": 2584,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866059.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866074.1",
"protein_id": "ENSP00000536133.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 642,
"cds_start": 63,
"cds_end": null,
"cds_length": 1929,
"cdna_start": 699,
"cdna_end": null,
"cdna_length": 2621,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866074.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968308.1",
"protein_id": "ENSP00000638367.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 642,
"cds_start": 63,
"cds_end": null,
"cds_length": 1929,
"cdna_start": 1970,
"cdna_end": null,
"cdna_length": 3892,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968308.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968307.1",
"protein_id": "ENSP00000638366.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 641,
"cds_start": 63,
"cds_end": null,
"cds_length": 1926,
"cdna_start": 603,
"cdna_end": null,
"cdna_length": 2493,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968307.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866069.1",
"protein_id": "ENSP00000536128.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 613,
"cds_start": 63,
"cds_end": null,
"cds_length": 1842,
"cdna_start": 606,
"cdna_end": null,
"cdna_length": 2441,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866069.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000923826.1",
"protein_id": "ENSP00000593885.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 613,
"cds_start": 63,
"cds_end": null,
"cds_length": 1842,
"cdna_start": 415,
"cdna_end": null,
"cdna_length": 2250,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000923826.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000468577.6",
"protein_id": "ENSP00000418883.2",
"transcript_support_level": 5,
"aa_start": 21,
"aa_end": null,
"aa_length": 612,
"cds_start": 63,
"cds_end": null,
"cds_length": 1839,
"cdna_start": 63,
"cdna_end": null,
"cdna_length": 1839,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000468577.6"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968306.1",
"protein_id": "ENSP00000638365.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 612,
"cds_start": 63,
"cds_end": null,
"cds_length": 1839,
"cdna_start": 610,
"cdna_end": null,
"cdna_length": 2421,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968306.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968313.1",
"protein_id": "ENSP00000638372.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 612,
"cds_start": 63,
"cds_end": null,
"cds_length": 1839,
"cdna_start": 208,
"cdna_end": null,
"cdna_length": 2346,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968313.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000923828.1",
"protein_id": "ENSP00000593887.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 611,
"cds_start": 63,
"cds_end": null,
"cds_length": 1836,
"cdna_start": 311,
"cdna_end": null,
"cdna_length": 2931,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000923828.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "NM_001244812.3",
"protein_id": "NP_001231741.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 601,
"cds_start": 63,
"cds_end": null,
"cds_length": 1806,
"cdna_start": 228,
"cdna_end": null,
"cdna_length": 6510,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001244812.3"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000484350.5",
"protein_id": "ENSP00000417857.1",
"transcript_support_level": 2,
"aa_start": 21,
"aa_end": null,
"aa_length": 601,
"cds_start": 63,
"cds_end": null,
"cds_length": 1806,
"cdna_start": 217,
"cdna_end": null,
"cdna_length": 1996,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000484350.5"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866054.1",
"protein_id": "ENSP00000536113.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 601,
"cds_start": 63,
"cds_end": null,
"cds_length": 1806,
"cdna_start": 692,
"cdna_end": null,
"cdna_length": 3180,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866054.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866082.1",
"protein_id": "ENSP00000536141.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 601,
"cds_start": 63,
"cds_end": null,
"cds_length": 1806,
"cdna_start": 538,
"cdna_end": null,
"cdna_length": 2337,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866082.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968311.1",
"protein_id": "ENSP00000638370.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 601,
"cds_start": 63,
"cds_end": null,
"cds_length": 1806,
"cdna_start": 216,
"cdna_end": null,
"cdna_length": 2015,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968311.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968314.1",
"protein_id": "ENSP00000638373.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 601,
"cds_start": 63,
"cds_end": null,
"cds_length": 1806,
"cdna_start": 288,
"cdna_end": null,
"cdna_length": 2057,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968314.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000968315.1",
"protein_id": "ENSP00000638374.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 601,
"cds_start": 63,
"cds_end": null,
"cds_length": 1806,
"cdna_start": 387,
"cdna_end": null,
"cdna_length": 2165,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000968315.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866070.1",
"protein_id": "ENSP00000536129.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 600,
"cds_start": 63,
"cds_end": null,
"cds_length": 1803,
"cdna_start": 606,
"cdna_end": null,
"cdna_length": 2402,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866070.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866101.1",
"protein_id": "ENSP00000536160.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 600,
"cds_start": 63,
"cds_end": null,
"cds_length": 1803,
"cdna_start": 182,
"cdna_end": null,
"cdna_length": 1958,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866101.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000866057.1",
"protein_id": "ENSP00000536116.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 536,
"cds_start": 63,
"cds_end": null,
"cds_length": 1611,
"cdna_start": 838,
"cdna_end": null,
"cdna_length": 2442,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000866057.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000649431.2",
"protein_id": "ENSP00000498174.2",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 448,
"cds_start": 63,
"cds_end": null,
"cds_length": 1348,
"cdna_start": 311,
"cdna_end": null,
"cdna_length": 1596,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000649431.2"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "NM_001012505.2",
"protein_id": "NP_001012523.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 114,
"cds_start": 63,
"cds_end": null,
"cds_length": 345,
"cdna_start": 578,
"cdna_end": null,
"cdna_length": 882,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001012505.2"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000650295.1",
"protein_id": "ENSP00000497138.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 88,
"cds_start": 63,
"cds_end": null,
"cds_length": 268,
"cdna_start": 375,
"cdna_end": null,
"cdna_length": 580,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000650295.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000648895.1",
"protein_id": "ENSP00000497417.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 74,
"cds_start": 63,
"cds_end": null,
"cds_length": 227,
"cdna_start": 924,
"cdna_end": null,
"cdna_length": 1088,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000648895.1"
},
{
"aa_ref": "G",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly",
"transcript": "ENST00000648783.1",
"protein_id": "ENSP00000498063.1",
"transcript_support_level": null,
"aa_start": 21,
"aa_end": null,
"aa_length": 34,
"cds_start": 63,
"cds_end": null,
"cds_length": 107,
"cdna_start": 520,
"cdna_end": null,
"cdna_length": 564,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000648783.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.-153-85682C>G",
"hgvs_p": null,
"transcript": "ENST00000649513.1",
"protein_id": "ENSP00000497237.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 467,
"cds_start": null,
"cds_end": null,
"cds_length": 1404,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1578,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000649513.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.-19+98114C>G",
"hgvs_p": null,
"transcript": "ENST00000647614.1",
"protein_id": "ENSP00000497710.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 209,
"cds_start": null,
"cds_end": null,
"cds_length": 630,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 831,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000647614.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "n.63C>G",
"hgvs_p": null,
"transcript": "ENST00000327590.9",
"protein_id": "ENSP00000333560.4",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5813,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000327590.9"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "n.494C>G",
"hgvs_p": null,
"transcript": "ENST00000615603.5",
"protein_id": null,
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4967,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000615603.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "n.125C>G",
"hgvs_p": null,
"transcript": "ENST00000622151.4",
"protein_id": null,
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 429,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000622151.4"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "n.245C>G",
"hgvs_p": null,
"transcript": "ENST00000648107.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 545,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000648107.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "n.63C>G",
"hgvs_p": null,
"transcript": "ENST00000648321.1",
"protein_id": "ENSP00000498015.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2483,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000648321.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "n.63C>G",
"hgvs_p": null,
"transcript": "ENST00000648384.1",
"protein_id": "ENSP00000497976.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2433,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000648384.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "n.129C>G",
"hgvs_p": null,
"transcript": "ENST00000648662.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 429,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000648662.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "n.304C>G",
"hgvs_p": null,
"transcript": "ENST00000648826.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 775,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000648826.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ENSG00000285708",
"gene_hgnc_id": null,
"hgvs_c": "n.*327C>G",
"hgvs_p": null,
"transcript": "ENST00000650123.1",
"protein_id": "ENSP00000497033.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2559,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000650123.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "n.667C>G",
"hgvs_p": null,
"transcript": "NR_146142.3",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7089,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_146142.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "n.667C>G",
"hgvs_p": null,
"transcript": "NR_146143.3",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7086,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_146143.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ENSG00000285708",
"gene_hgnc_id": null,
"hgvs_c": "n.*327C>G",
"hgvs_p": null,
"transcript": "ENST00000650123.1",
"protein_id": "ENSP00000497033.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2559,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000650123.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"hgvs_c": "c.*12C>G",
"hgvs_p": null,
"transcript": "ENST00000650156.1",
"protein_id": "ENSP00000496852.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 16,
"cds_start": null,
"cds_end": null,
"cds_length": 51,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 584,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000650156.1"
}
],
"gene_symbol": "FOXP1",
"gene_hgnc_id": 3823,
"dbsnp": "rs376702675",
"frequency_reference_population": null,
"hom_count_reference_population": 0,
"allele_count_reference_population": 0,
"gnomad_exomes_af": null,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": null,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": null,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": -0.4300000071525574,
"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": null,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.43,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 2.41,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0,
"spliceai_max_prediction": "Benign",
"dbscsnv_ada_score": null,
"dbscsnv_ada_prediction": null,
"apogee2_score": null,
"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": -1,
"acmg_classification": "Likely_benign",
"acmg_criteria": "PM2,BP4_Moderate,BP7",
"acmg_by_gene": [
{
"score": -1,
"benign_score": 3,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate",
"BP7"
],
"verdict": "Likely_benign",
"transcript": "NM_001244810.2",
"gene_symbol": "FOXP1",
"hgnc_id": 3823,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly"
},
{
"score": -1,
"benign_score": 3,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate",
"BP7"
],
"verdict": "Likely_benign",
"transcript": "ENST00000647725.1",
"gene_symbol": "ENSG00000285708",
"hgnc_id": null,
"effects": [
"synonymous_variant"
],
"inheritance_mode": "",
"hgvs_c": "c.63C>G",
"hgvs_p": "p.Gly21Gly"
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}