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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: 15-81290527-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=81290527&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "15",
"pos": 81290527,
"ref": "G",
"alt": "A",
"effect": "synonymous_variant",
"transcript": "ENST00000683961.1",
"consequences": [
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.1407G>A",
"hgvs_p": "p.Gln469Gln",
"transcript": "NM_172217.5",
"protein_id": "NP_757366.2",
"transcript_support_level": null,
"aa_start": 469,
"aa_end": null,
"aa_length": 1332,
"cds_start": 1407,
"cds_end": null,
"cds_length": 3999,
"cdna_start": 1782,
"cdna_end": null,
"cdna_length": 9634,
"mane_select": "ENST00000683961.1",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.1407G>A",
"hgvs_p": "p.Gln469Gln",
"transcript": "ENST00000683961.1",
"protein_id": "ENSP00000508085.1",
"transcript_support_level": null,
"aa_start": 469,
"aa_end": null,
"aa_length": 1332,
"cds_start": 1407,
"cds_end": null,
"cds_length": 3999,
"cdna_start": 1782,
"cdna_end": null,
"cdna_length": 9634,
"mane_select": "NM_172217.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.1548G>A",
"hgvs_p": "p.Gln516Gln",
"transcript": "ENST00000302987.10",
"protein_id": "ENSP00000302935.5",
"transcript_support_level": 1,
"aa_start": 516,
"aa_end": null,
"aa_length": 1378,
"cds_start": 1548,
"cds_end": null,
"cds_length": 4137,
"cdna_start": 1693,
"cdna_end": null,
"cdna_length": 9542,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"5_prime_UTR_premature_start_codon_gain_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.-613G>A",
"hgvs_p": null,
"transcript": "NM_001352684.2",
"protein_id": "NP_001339613.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 722,
"cds_start": -4,
"cds_end": null,
"cds_length": 2169,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9823,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.1560G>A",
"hgvs_p": "p.Gln520Gln",
"transcript": "NM_001352686.2",
"protein_id": "NP_001339615.1",
"transcript_support_level": null,
"aa_start": 520,
"aa_end": null,
"aa_length": 1382,
"cds_start": 1560,
"cds_end": null,
"cds_length": 4149,
"cdna_start": 1895,
"cdna_end": null,
"cdna_length": 9744,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.1548G>A",
"hgvs_p": "p.Gln516Gln",
"transcript": "NM_001438661.1",
"protein_id": "NP_001425590.1",
"transcript_support_level": null,
"aa_start": 516,
"aa_end": null,
"aa_length": 1379,
"cds_start": 1548,
"cds_end": null,
"cds_length": 4140,
"cdna_start": 1693,
"cdna_end": null,
"cdna_length": 9545,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.1407G>A",
"hgvs_p": "p.Gln469Gln",
"transcript": "NM_001172128.2",
"protein_id": "NP_001165599.1",
"transcript_support_level": null,
"aa_start": 469,
"aa_end": null,
"aa_length": 1331,
"cds_start": 1407,
"cds_end": null,
"cds_length": 3996,
"cdna_start": 1767,
"cdna_end": null,
"cdna_length": 9616,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.1407G>A",
"hgvs_p": "p.Gln469Gln",
"transcript": "ENST00000394660.6",
"protein_id": "ENSP00000378155.2",
"transcript_support_level": 2,
"aa_start": 469,
"aa_end": null,
"aa_length": 1331,
"cds_start": 1407,
"cds_end": null,
"cds_length": 3996,
"cdna_start": 1767,
"cdna_end": null,
"cdna_length": 9616,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.1407G>A",
"hgvs_p": "p.Gln469Gln",
"transcript": "ENST00000706926.1",
"protein_id": "ENSP00000516648.1",
"transcript_support_level": null,
"aa_start": 469,
"aa_end": null,
"aa_length": 1331,
"cds_start": 1407,
"cds_end": null,
"cds_length": 3996,
"cdna_start": 1895,
"cdna_end": null,
"cdna_length": 9744,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.897G>A",
"hgvs_p": "p.Gln299Gln",
"transcript": "NM_001352685.2",
"protein_id": "NP_001339614.1",
"transcript_support_level": null,
"aa_start": 299,
"aa_end": null,
"aa_length": 1161,
"cds_start": 897,
"cds_end": null,
"cds_length": 3486,
"cdna_start": 1930,
"cdna_end": null,
"cdna_length": 9779,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.1407G>A",
"hgvs_p": "p.Gln469Gln",
"transcript": "ENST00000559383.5",
"protein_id": "ENSP00000453250.1",
"transcript_support_level": 2,
"aa_start": 469,
"aa_end": null,
"aa_length": 593,
"cds_start": 1407,
"cds_end": null,
"cds_length": 1782,
"cdna_start": 1783,
"cdna_end": null,
"cdna_length": 2158,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.1599G>A",
"hgvs_p": "p.Gln533Gln",
"transcript": "XM_047432447.1",
"protein_id": "XP_047288403.1",
"transcript_support_level": null,
"aa_start": 533,
"aa_end": null,
"aa_length": 1396,
"cds_start": 1599,
"cds_end": null,
"cds_length": 4191,
"cdna_start": 1744,
"cdna_end": null,
"cdna_length": 9596,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.1599G>A",
"hgvs_p": "p.Gln533Gln",
"transcript": "XM_047432448.1",
"protein_id": "XP_047288404.1",
"transcript_support_level": null,
"aa_start": 533,
"aa_end": null,
"aa_length": 1395,
"cds_start": 1599,
"cds_end": null,
"cds_length": 4188,
"cdna_start": 1744,
"cdna_end": null,
"cdna_length": 9593,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.1548G>A",
"hgvs_p": "p.Gln516Gln",
"transcript": "XM_047432450.1",
"protein_id": "XP_047288406.1",
"transcript_support_level": null,
"aa_start": 516,
"aa_end": null,
"aa_length": 1378,
"cds_start": 1548,
"cds_end": null,
"cds_length": 4137,
"cdna_start": 1693,
"cdna_end": null,
"cdna_length": 9542,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.1599G>A",
"hgvs_p": "p.Gln533Gln",
"transcript": "XM_047432451.1",
"protein_id": "XP_047288407.1",
"transcript_support_level": null,
"aa_start": 533,
"aa_end": null,
"aa_length": 1335,
"cds_start": 1599,
"cds_end": null,
"cds_length": 4008,
"cdna_start": 1744,
"cdna_end": null,
"cdna_length": 5166,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.1599G>A",
"hgvs_p": "p.Gln533Gln",
"transcript": "XM_047432452.1",
"protein_id": "XP_047288408.1",
"transcript_support_level": null,
"aa_start": 533,
"aa_end": null,
"aa_length": 1334,
"cds_start": 1599,
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"cdna_start": 1744,
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"cdna_length": 5163,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.1407G>A",
"hgvs_p": "p.Gln469Gln",
"transcript": "XM_047432453.1",
"protein_id": "XP_047288409.1",
"transcript_support_level": null,
"aa_start": 469,
"aa_end": null,
"aa_length": 1332,
"cds_start": 1407,
"cds_end": null,
"cds_length": 3999,
"cdna_start": 1578,
"cdna_end": null,
"cdna_length": 9430,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.897G>A",
"hgvs_p": "p.Gln299Gln",
"transcript": "XM_047432454.1",
"protein_id": "XP_047288410.1",
"transcript_support_level": null,
"aa_start": 299,
"aa_end": null,
"aa_length": 1162,
"cds_start": 897,
"cds_end": null,
"cds_length": 3489,
"cdna_start": 952,
"cdna_end": null,
"cdna_length": 8804,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.1599G>A",
"hgvs_p": "p.Gln533Gln",
"transcript": "XM_047432455.1",
"protein_id": "XP_047288411.1",
"transcript_support_level": null,
"aa_start": 533,
"aa_end": null,
"aa_length": 762,
"cds_start": 1599,
"cds_end": null,
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"cdna_start": 1744,
"cdna_end": null,
"cdna_length": 2687,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "Q",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "c.1599G>A",
"hgvs_p": "p.Gln533Gln",
"transcript": "XM_047432458.1",
"protein_id": "XP_047288414.1",
"transcript_support_level": null,
"aa_start": 533,
"aa_end": null,
"aa_length": 714,
"cds_start": 1599,
"cds_end": null,
"cds_length": 2145,
"cdna_start": 1744,
"cdna_end": null,
"cdna_length": 3930,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "n.1407G>A",
"hgvs_p": null,
"transcript": "ENST00000360547.9",
"protein_id": "ENSP00000456972.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5120,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
"gene_hgnc_id": 5980,
"hgvs_c": "n.555G>A",
"hgvs_p": null,
"transcript": "ENST00000560115.5",
"protein_id": "ENSP00000454636.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3775,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IL16",
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"hgvs_c": "n.*184G>A",
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{
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{
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{
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],
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"computational_prediction_selected": "Benign",
"computational_source_selected": "BayesDel_noAF",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
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"bayesdelnoaf_score": -0.59,
"bayesdelnoaf_prediction": "Benign",
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"phylop100way_prediction": "Benign",
"spliceai_max_score": 0,
"spliceai_max_prediction": "Benign",
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"acmg_score": -13,
"acmg_classification": "Benign",
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"acmg_by_gene": [
{
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"criteria": [
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"BP7",
"BA1"
],
"verdict": "Benign",
"transcript": "ENST00000683961.1",
"gene_symbol": "IL16",
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"effects": [
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],
"inheritance_mode": "AR",
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],
"clinvar_disease": "",
"clinvar_classification": "",
"clinvar_review_status": "",
"clinvar_submissions_summary": "",
"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}