← 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: 2-37645960-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=37645960&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 37645960,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_006449.5",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "NM_006449.5",
"protein_id": "NP_006440.2",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1080,
"cdna_end": null,
"cdna_length": 5096,
"mane_select": "ENST00000295324.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_006449.5"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000295324.4",
"protein_id": "ENSP00000295324.3",
"transcript_support_level": 1,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1080,
"cdna_end": null,
"cdna_length": 5096,
"mane_select": "NM_006449.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000295324.4"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "NM_001270436.2",
"protein_id": "NP_001257365.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 966,
"cdna_end": null,
"cdna_length": 4982,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001270436.2"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "NM_001270437.2",
"protein_id": "NP_001257366.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1022,
"cdna_end": null,
"cdna_length": 5038,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001270437.2"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "NM_001270438.2",
"protein_id": "NP_001257367.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 998,
"cdna_end": null,
"cdna_length": 5014,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001270438.2"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "NM_001371569.1",
"protein_id": "NP_001358498.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 984,
"cdna_end": null,
"cdna_length": 5000,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001371569.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "NM_001371570.1",
"protein_id": "NP_001358499.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 971,
"cdna_end": null,
"cdna_length": 4987,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001371570.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000611976.1",
"protein_id": "ENSP00000480549.1",
"transcript_support_level": 3,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1046,
"cdna_end": null,
"cdna_length": 5124,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000611976.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000885380.1",
"protein_id": "ENSP00000555439.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1006,
"cdna_end": null,
"cdna_length": 2114,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885380.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000885381.1",
"protein_id": "ENSP00000555440.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1084,
"cdna_end": null,
"cdna_length": 3070,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885381.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000885382.1",
"protein_id": "ENSP00000555441.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 971,
"cdna_end": null,
"cdna_length": 2912,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885382.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000885383.1",
"protein_id": "ENSP00000555442.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1719,
"cdna_end": null,
"cdna_length": 2840,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885383.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000885384.1",
"protein_id": "ENSP00000555443.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1614,
"cdna_end": null,
"cdna_length": 2735,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885384.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000927367.1",
"protein_id": "ENSP00000597426.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1338,
"cdna_end": null,
"cdna_length": 5355,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000927367.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000927368.1",
"protein_id": "ENSP00000597427.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 2334,
"cdna_end": null,
"cdna_length": 3138,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000927368.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000927369.1",
"protein_id": "ENSP00000597428.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 941,
"cdna_end": null,
"cdna_length": 1747,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000927369.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000927370.1",
"protein_id": "ENSP00000597429.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1174,
"cdna_end": null,
"cdna_length": 1978,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000927370.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000927371.1",
"protein_id": "ENSP00000597430.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1139,
"cdna_end": null,
"cdna_length": 3125,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000927371.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000956783.1",
"protein_id": "ENSP00000626842.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1375,
"cdna_end": null,
"cdna_length": 3361,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000956783.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000956784.1",
"protein_id": "ENSP00000626843.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1512,
"cdna_end": null,
"cdna_length": 2635,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000956784.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000956785.1",
"protein_id": "ENSP00000626844.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1674,
"cdna_end": null,
"cdna_length": 2790,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000956785.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000956786.1",
"protein_id": "ENSP00000626845.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1526,
"cdna_end": null,
"cdna_length": 2643,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000956786.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000956787.1",
"protein_id": "ENSP00000626846.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1458,
"cdna_end": null,
"cdna_length": 2580,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000956787.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000956788.1",
"protein_id": "ENSP00000626847.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1532,
"cdna_end": null,
"cdna_length": 2336,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000956788.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000956789.1",
"protein_id": "ENSP00000626848.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1547,
"cdna_end": null,
"cdna_length": 2354,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000956789.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000956790.1",
"protein_id": "ENSP00000626849.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1308,
"cdna_end": null,
"cdna_length": 2106,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000956790.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000956791.1",
"protein_id": "ENSP00000626850.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 1490,
"cdna_end": null,
"cdna_length": 2289,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000956791.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "ENST00000457889.1",
"protein_id": "ENSP00000403298.1",
"transcript_support_level": 2,
"aa_start": 210,
"aa_end": null,
"aa_length": 214,
"cds_start": 628,
"cds_end": null,
"cds_length": 647,
"cdna_start": 978,
"cdna_end": null,
"cdna_length": 997,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000457889.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala",
"transcript": "XM_011532482.4",
"protein_id": "XP_011530784.1",
"transcript_support_level": null,
"aa_start": 210,
"aa_end": null,
"aa_length": 254,
"cds_start": 628,
"cds_end": null,
"cds_length": 765,
"cdna_start": 2914,
"cdna_end": null,
"cdna_length": 6930,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011532482.4"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.526-716G>C",
"hgvs_p": null,
"transcript": "ENST00000419425.1",
"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": 548,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000419425.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.105-15655G>C",
"hgvs_p": null,
"transcript": "ENST00000702971.2",
"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": 582,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000702971.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.659-15655G>C",
"hgvs_p": null,
"transcript": "ENST00000715737.1",
"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": 1140,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000715737.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.469+74768G>C",
"hgvs_p": null,
"transcript": "ENST00000751609.1",
"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": 1032,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751609.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.469+74768G>C",
"hgvs_p": null,
"transcript": "ENST00000751610.1",
"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": 1344,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751610.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.282-43098G>C",
"hgvs_p": null,
"transcript": "ENST00000751611.1",
"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": 790,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751611.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.470-43098G>C",
"hgvs_p": null,
"transcript": "ENST00000751612.1",
"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": 977,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751612.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.313-43098G>C",
"hgvs_p": null,
"transcript": "ENST00000751613.1",
"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": 820,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751613.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.406+28529G>C",
"hgvs_p": null,
"transcript": "ENST00000751614.1",
"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": 918,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751614.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.588-15655G>C",
"hgvs_p": null,
"transcript": "ENST00000751615.1",
"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": 1486,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751615.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.287-15655G>C",
"hgvs_p": null,
"transcript": "ENST00000751616.1",
"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": 1185,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751616.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.365-19369G>C",
"hgvs_p": null,
"transcript": "ENST00000751617.1",
"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": 536,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751617.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.313-19369G>C",
"hgvs_p": null,
"transcript": "ENST00000751618.1",
"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": 484,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751618.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.496-19369G>C",
"hgvs_p": null,
"transcript": "ENST00000751619.1",
"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": 667,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751619.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.464-15655G>C",
"hgvs_p": null,
"transcript": "ENST00000751620.1",
"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": 770,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751620.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.302-19369G>C",
"hgvs_p": null,
"transcript": "ENST00000751621.1",
"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": 473,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751621.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.285-15655G>C",
"hgvs_p": null,
"transcript": "ENST00000751622.1",
"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": 1183,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751622.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.470-15655G>C",
"hgvs_p": null,
"transcript": "ENST00000751623.1",
"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": 946,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751623.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.365-15655G>C",
"hgvs_p": null,
"transcript": "ENST00000751624.1",
"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": 841,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751624.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.556-15655G>C",
"hgvs_p": null,
"transcript": "ENST00000751625.1",
"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": 802,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751625.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.313-15655G>C",
"hgvs_p": null,
"transcript": "ENST00000751626.1",
"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": 557,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751626.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.416-8039G>C",
"hgvs_p": null,
"transcript": "ENST00000751627.1",
"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": 552,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751627.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.577-716G>C",
"hgvs_p": null,
"transcript": "ENST00000751629.1",
"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": 1168,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751629.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.234+33702G>C",
"hgvs_p": null,
"transcript": "ENST00000751683.1",
"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": 746,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751683.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.247-19369G>C",
"hgvs_p": null,
"transcript": "ENST00000751691.1",
"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": 422,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751691.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.241+19407G>C",
"hgvs_p": null,
"transcript": "ENST00000751692.1",
"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": 747,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751692.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.257-15655G>C",
"hgvs_p": null,
"transcript": "ENST00000751693.1",
"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": 733,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751693.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.208-15655G>C",
"hgvs_p": null,
"transcript": "ENST00000751714.1",
"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": 408,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751714.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "CDC42EP3-AS1",
"gene_hgnc_id": 56370,
"hgvs_c": "n.187+13560G>C",
"hgvs_p": null,
"transcript": "ENST00000751715.1",
"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": 439,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000751715.1"
}
],
"gene_symbol": "CDC42EP3",
"gene_hgnc_id": 16943,
"dbsnp": "rs200546253",
"frequency_reference_population": 6.8408997e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 6.8409e-7,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 1,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.07923257350921631,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.014,
"revel_prediction": "Benign",
"alphamissense_score": 0.0601,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.64,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 1.316,
"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": 0,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4_Moderate",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "NM_006449.5",
"gene_symbol": "CDC42EP3",
"hgnc_id": 16943,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.628C>G",
"hgvs_p": "p.Pro210Ala"
},
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "ENST00000419425.1",
"gene_symbol": "CDC42EP3-AS1",
"hgnc_id": 56370,
"effects": [
"intron_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.526-716G>C",
"hgvs_p": null
}
],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}