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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: 14-31066242-C-CT (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=31066242&ref=C&alt=CT&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "14",
"pos": 31066242,
"ref": "C",
"alt": "CT",
"effect": "frameshift_variant",
"transcript": "NM_007077.5",
"consequences": [
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "NM_001128126.3",
"protein_id": "NP_001121598.1",
"transcript_support_level": null,
"aa_start": 17,
"aa_end": null,
"aa_length": 144,
"cds_start": 50,
"cds_end": null,
"cds_length": 435,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000542754.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001128126.3"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "ENST00000542754.7",
"protein_id": "ENSP00000438170.2",
"transcript_support_level": 1,
"aa_start": 17,
"aa_end": null,
"aa_length": 144,
"cds_start": 50,
"cds_end": null,
"cds_length": 435,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001128126.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000542754.7"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "ENST00000334725.8",
"protein_id": "ENSP00000334484.4",
"transcript_support_level": 1,
"aa_start": 17,
"aa_end": null,
"aa_length": 149,
"cds_start": 50,
"cds_end": null,
"cds_length": 450,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000334725.8"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "ENST00000216366.9",
"protein_id": "ENSP00000216366.5",
"transcript_support_level": 1,
"aa_start": 17,
"aa_end": null,
"aa_length": 132,
"cds_start": 50,
"cds_end": null,
"cds_length": 399,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000216366.9"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "ENST00000313566.11",
"protein_id": "ENSP00000322508.8",
"transcript_support_level": 3,
"aa_start": 17,
"aa_end": null,
"aa_length": 173,
"cds_start": 50,
"cds_end": null,
"cds_length": 522,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000313566.11"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "NM_007077.5",
"protein_id": "NP_009008.2",
"transcript_support_level": null,
"aa_start": 17,
"aa_end": null,
"aa_length": 159,
"cds_start": 50,
"cds_end": null,
"cds_length": 480,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_007077.5"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "ENST00000554345.6",
"protein_id": "ENSP00000450768.2",
"transcript_support_level": 3,
"aa_start": 17,
"aa_end": null,
"aa_length": 159,
"cds_start": 50,
"cds_end": null,
"cds_length": 480,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000554345.6"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "NM_001254727.2",
"protein_id": "NP_001241656.1",
"transcript_support_level": null,
"aa_start": 17,
"aa_end": null,
"aa_length": 149,
"cds_start": 50,
"cds_end": null,
"cds_length": 450,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001254727.2"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "NM_001254728.2",
"protein_id": "NP_001241657.1",
"transcript_support_level": null,
"aa_start": 17,
"aa_end": null,
"aa_length": 144,
"cds_start": 50,
"cds_end": null,
"cds_length": 435,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001254728.2"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "NM_001254729.2",
"protein_id": "NP_001241658.1",
"transcript_support_level": null,
"aa_start": 17,
"aa_end": null,
"aa_length": 144,
"cds_start": 50,
"cds_end": null,
"cds_length": 435,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001254729.2"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "ENST00000555417.6",
"protein_id": "ENSP00000451609.2",
"transcript_support_level": 3,
"aa_start": 17,
"aa_end": null,
"aa_length": 144,
"cds_start": 50,
"cds_end": null,
"cds_length": 435,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000555417.6"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "ENST00000556232.8",
"protein_id": "ENSP00000451918.3",
"transcript_support_level": 4,
"aa_start": 17,
"aa_end": null,
"aa_length": 144,
"cds_start": 50,
"cds_end": null,
"cds_length": 435,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000556232.8"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "ENST00000557346.6",
"protein_id": "ENSP00000451479.2",
"transcript_support_level": 3,
"aa_start": 17,
"aa_end": null,
"aa_length": 144,
"cds_start": 50,
"cds_end": null,
"cds_length": 435,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000557346.6"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "ENST00000713810.1",
"protein_id": "ENSP00000519116.1",
"transcript_support_level": null,
"aa_start": 17,
"aa_end": null,
"aa_length": 144,
"cds_start": 50,
"cds_end": null,
"cds_length": 435,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000713810.1"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "ENST00000964657.1",
"protein_id": "ENSP00000634716.1",
"transcript_support_level": null,
"aa_start": 17,
"aa_end": null,
"aa_length": 144,
"cds_start": 50,
"cds_end": null,
"cds_length": 435,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000964657.1"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "ENST00000964659.1",
"protein_id": "ENSP00000634718.1",
"transcript_support_level": null,
"aa_start": 17,
"aa_end": null,
"aa_length": 144,
"cds_start": 50,
"cds_end": null,
"cds_length": 435,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000964659.1"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "NM_001254726.2",
"protein_id": "NP_001241655.1",
"transcript_support_level": null,
"aa_start": 17,
"aa_end": null,
"aa_length": 135,
"cds_start": 50,
"cds_end": null,
"cds_length": 408,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001254726.2"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "ENST00000554609.6",
"protein_id": "ENSP00000452383.2",
"transcript_support_level": 5,
"aa_start": 17,
"aa_end": null,
"aa_length": 135,
"cds_start": 50,
"cds_end": null,
"cds_length": 408,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000554609.6"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "ENST00000673317.1",
"protein_id": "ENSP00000500890.1",
"transcript_support_level": null,
"aa_start": 17,
"aa_end": null,
"aa_length": 135,
"cds_start": 50,
"cds_end": null,
"cds_length": 408,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000673317.1"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "ENST00000713808.1",
"protein_id": "ENSP00000519114.1",
"transcript_support_level": null,
"aa_start": 17,
"aa_end": null,
"aa_length": 130,
"cds_start": 50,
"cds_end": null,
"cds_length": 393,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000713808.1"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "ENST00000964658.1",
"protein_id": "ENSP00000634717.1",
"transcript_support_level": null,
"aa_start": 17,
"aa_end": null,
"aa_length": 121,
"cds_start": 50,
"cds_end": null,
"cds_length": 366,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000964658.1"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs",
"transcript": "ENST00000713807.1",
"protein_id": "ENSP00000519113.1",
"transcript_support_level": null,
"aa_start": 17,
"aa_end": null,
"aa_length": 102,
"cds_start": 50,
"cds_end": null,
"cds_length": 309,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000713807.1"
},
{
"aa_ref": "S",
"aa_alt": "F?",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"frameshift_variant"
],
"exon_rank": 3,
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},
{
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"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": 3,
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},
{
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],
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},
{
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"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
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"gene_symbol": "AP4S1",
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"transcript": "ENST00000672143.1",
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"biotype": "nonsense_mediated_decay",
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},
{
"aa_ref": null,
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"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
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"gene_symbol": "AP4S1",
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"feature": "ENST00000673001.1"
},
{
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"protein_coding": false,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
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"exon_count": 3,
"intron_rank": null,
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"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"hgvs_c": "n.-54_-53insT",
"hgvs_p": null,
"transcript": "ENST00000556480.1",
"protein_id": null,
"transcript_support_level": 3,
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"aa_end": null,
"aa_length": null,
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"cds_end": null,
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"cdna_start": null,
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"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000556480.1"
}
],
"gene_symbol": "AP4S1",
"gene_hgnc_id": 575,
"dbsnp": "rs2139569112",
"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": null,
"computational_prediction_selected": null,
"computational_source_selected": null,
"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": null,
"bayesdelnoaf_prediction": null,
"phylop100way_score": 6.738,
"phylop100way_prediction": "Uncertain_significance",
"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": 7,
"acmg_classification": "Likely_pathogenic",
"acmg_criteria": "PVS1_Strong,PM2,PP5",
"acmg_by_gene": [
{
"score": 7,
"benign_score": 0,
"pathogenic_score": 7,
"criteria": [
"PVS1_Strong",
"PM2",
"PP5"
],
"verdict": "Likely_pathogenic",
"transcript": "NM_007077.5",
"gene_symbol": "AP4S1",
"hgnc_id": 575,
"effects": [
"frameshift_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.49dupT",
"hgvs_p": "p.Ser17fs"
}
],
"clinvar_disease": "Spastic paraplegia",
"clinvar_classification": "Likely pathogenic",
"clinvar_review_status": "no assertion criteria provided",
"clinvar_submissions_summary": "null",
"phenotype_combined": "Spastic paraplegia",
"pathogenicity_classification_combined": "Likely pathogenic",
"custom_annotations": null
}
],
"message": null
}