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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: 10-27014676-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=27014676&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "10",
"pos": 27014676,
"ref": "A",
"alt": "G",
"effect": "synonymous_variant",
"transcript": "ENST00000376087.5",
"consequences": [
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 31,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.4542T>C",
"hgvs_p": "p.Phe1514Phe",
"transcript": "NM_014915.3",
"protein_id": "NP_055730.2",
"transcript_support_level": null,
"aa_start": 1514,
"aa_end": null,
"aa_length": 1710,
"cds_start": 4542,
"cds_end": null,
"cds_length": 5133,
"cdna_start": 4710,
"cdna_end": null,
"cdna_length": 6775,
"mane_select": "ENST00000376087.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 31,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.4542T>C",
"hgvs_p": "p.Phe1514Phe",
"transcript": "ENST00000376087.5",
"protein_id": "ENSP00000365255.4",
"transcript_support_level": 5,
"aa_start": 1514,
"aa_end": null,
"aa_length": 1710,
"cds_start": 4542,
"cds_end": null,
"cds_length": 5133,
"cdna_start": 4710,
"cdna_end": null,
"cdna_length": 6775,
"mane_select": "NM_014915.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 31,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.4539T>C",
"hgvs_p": "p.Phe1513Phe",
"transcript": "ENST00000436985.7",
"protein_id": "ENSP00000405112.3",
"transcript_support_level": 1,
"aa_start": 1513,
"aa_end": null,
"aa_length": 1709,
"cds_start": 4539,
"cds_end": null,
"cds_length": 5130,
"cdna_start": 4698,
"cdna_end": null,
"cdna_length": 5564,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 31,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.4539T>C",
"hgvs_p": "p.Phe1513Phe",
"transcript": "NM_001256053.2",
"protein_id": "NP_001242982.1",
"transcript_support_level": null,
"aa_start": 1513,
"aa_end": null,
"aa_length": 1709,
"cds_start": 4539,
"cds_end": null,
"cds_length": 5130,
"cdna_start": 4707,
"cdna_end": null,
"cdna_length": 6772,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.3T>C",
"hgvs_p": "p.Phe1Phe",
"transcript": "ENST00000445828.5",
"protein_id": "ENSP00000394152.1",
"transcript_support_level": 5,
"aa_start": 1,
"aa_end": null,
"aa_length": 212,
"cds_start": 3,
"cds_end": null,
"cds_length": 639,
"cdna_start": 4,
"cdna_end": null,
"cdna_length": 761,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 32,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.5628T>C",
"hgvs_p": "p.Phe1876Phe",
"transcript": "XM_017015928.2",
"protein_id": "XP_016871417.1",
"transcript_support_level": null,
"aa_start": 1876,
"aa_end": null,
"aa_length": 2112,
"cds_start": 5628,
"cds_end": null,
"cds_length": 6339,
"cdna_start": 5796,
"cdna_end": null,
"cdna_length": 10915,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 32,
"exon_rank_end": null,
"exon_count": 41,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.5628T>C",
"hgvs_p": "p.Phe1876Phe",
"transcript": "XM_047424821.1",
"protein_id": "XP_047280777.1",
"transcript_support_level": null,
"aa_start": 1876,
"aa_end": null,
"aa_length": 2112,
"cds_start": 5628,
"cds_end": null,
"cds_length": 6339,
"cdna_start": 5796,
"cdna_end": null,
"cdna_length": 7997,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 32,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.5628T>C",
"hgvs_p": "p.Phe1876Phe",
"transcript": "XM_047424822.1",
"protein_id": "XP_047280778.1",
"transcript_support_level": null,
"aa_start": 1876,
"aa_end": null,
"aa_length": 2112,
"cds_start": 5628,
"cds_end": null,
"cds_length": 6339,
"cdna_start": 5796,
"cdna_end": null,
"cdna_length": 9178,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 33,
"exon_rank_end": null,
"exon_count": 41,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.5616T>C",
"hgvs_p": "p.Phe1872Phe",
"transcript": "XM_017015929.2",
"protein_id": "XP_016871418.1",
"transcript_support_level": null,
"aa_start": 1872,
"aa_end": null,
"aa_length": 2108,
"cds_start": 5616,
"cds_end": null,
"cds_length": 6327,
"cdna_start": 5784,
"cdna_end": null,
"cdna_length": 15604,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 32,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.5628T>C",
"hgvs_p": "p.Phe1876Phe",
"transcript": "XM_006717423.3",
"protein_id": "XP_006717486.1",
"transcript_support_level": null,
"aa_start": 1876,
"aa_end": null,
"aa_length": 2072,
"cds_start": 5628,
"cds_end": null,
"cds_length": 6219,
"cdna_start": 5796,
"cdna_end": null,
"cdna_length": 7861,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 32,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.5625T>C",
"hgvs_p": "p.Phe1875Phe",
"transcript": "XM_047424824.1",
"protein_id": "XP_047280780.1",
"transcript_support_level": null,
"aa_start": 1875,
"aa_end": null,
"aa_length": 2071,
"cds_start": 5625,
"cds_end": null,
"cds_length": 6216,
"cdna_start": 5793,
"cdna_end": null,
"cdna_length": 7858,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 32,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.5628T>C",
"hgvs_p": "p.Phe1876Phe",
"transcript": "XM_011519416.3",
"protein_id": "XP_011517718.1",
"transcript_support_level": null,
"aa_start": 1876,
"aa_end": null,
"aa_length": 2062,
"cds_start": 5628,
"cds_end": null,
"cds_length": 6189,
"cdna_start": 5796,
"cdna_end": null,
"cdna_length": 7036,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 32,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.5628T>C",
"hgvs_p": "p.Phe1876Phe",
"transcript": "XM_047424825.1",
"protein_id": "XP_047280781.1",
"transcript_support_level": null,
"aa_start": 1876,
"aa_end": null,
"aa_length": 2062,
"cds_start": 5628,
"cds_end": null,
"cds_length": 6189,
"cdna_start": 5796,
"cdna_end": null,
"cdna_length": 6469,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 32,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.5628T>C",
"hgvs_p": "p.Phe1876Phe",
"transcript": "XM_006717425.5",
"protein_id": "XP_006717488.1",
"transcript_support_level": null,
"aa_start": 1876,
"aa_end": null,
"aa_length": 2031,
"cds_start": 5628,
"cds_end": null,
"cds_length": 6096,
"cdna_start": 5796,
"cdna_end": null,
"cdna_length": 9532,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 32,
"exon_rank_end": null,
"exon_count": 36,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.5628T>C",
"hgvs_p": "p.Phe1876Phe",
"transcript": "XM_017015932.2",
"protein_id": "XP_016871421.1",
"transcript_support_level": null,
"aa_start": 1876,
"aa_end": null,
"aa_length": 2031,
"cds_start": 5628,
"cds_end": null,
"cds_length": 6096,
"cdna_start": 5796,
"cdna_end": null,
"cdna_length": 6896,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 31,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.5337T>C",
"hgvs_p": "p.Phe1779Phe",
"transcript": "XM_047424826.1",
"protein_id": "XP_047280782.1",
"transcript_support_level": null,
"aa_start": 1779,
"aa_end": null,
"aa_length": 1975,
"cds_start": 5337,
"cds_end": null,
"cds_length": 5928,
"cdna_start": 5505,
"cdna_end": null,
"cdna_length": 7570,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.4440T>C",
"hgvs_p": "p.Phe1480Phe",
"transcript": "XM_047424827.1",
"protein_id": "XP_047280783.1",
"transcript_support_level": null,
"aa_start": 1480,
"aa_end": null,
"aa_length": 1676,
"cds_start": 4440,
"cds_end": null,
"cds_length": 5031,
"cdna_start": 4608,
"cdna_end": null,
"cdna_length": 6673,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 31,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.4542T>C",
"hgvs_p": "p.Phe1514Phe",
"transcript": "XM_047424828.1",
"protein_id": "XP_047280784.1",
"transcript_support_level": null,
"aa_start": 1514,
"aa_end": null,
"aa_length": 1669,
"cds_start": 4542,
"cds_end": null,
"cds_length": 5010,
"cdna_start": 4710,
"cdna_end": null,
"cdna_length": 8446,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 31,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.4539T>C",
"hgvs_p": "p.Phe1513Phe",
"transcript": "XM_047424830.1",
"protein_id": "XP_047280786.1",
"transcript_support_level": null,
"aa_start": 1513,
"aa_end": null,
"aa_length": 1668,
"cds_start": 4539,
"cds_end": null,
"cds_length": 5007,
"cdna_start": 4707,
"cdna_end": null,
"cdna_length": 5807,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "F",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"synonymous_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 34,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "c.4440T>C",
"hgvs_p": "p.Phe1480Phe",
"transcript": "XM_047424832.1",
"protein_id": "XP_047280788.1",
"transcript_support_level": null,
"aa_start": 1480,
"aa_end": null,
"aa_length": 1635,
"cds_start": 4440,
"cds_end": null,
"cds_length": 4908,
"cdna_start": 4608,
"cdna_end": null,
"cdna_length": 5708,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "n.30T>C",
"hgvs_p": null,
"transcript": "ENST00000674670.1",
"protein_id": "ENSP00000502448.1",
"transcript_support_level": null,
"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": 3045,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ANKRD26",
"gene_hgnc_id": 29186,
"hgvs_c": "n.*865T>C",
"hgvs_p": null,
"transcript": "ENST00000675116.1",
"protein_id": "ENSP00000501975.1",
"transcript_support_level": null,
"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": 3314,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
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{
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{
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],
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"splice_prediction_selected": "Benign",
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"bayesdelnoaf_score": -0.56,
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"phylop100way_prediction": "Benign",
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"acmg_classification": "Likely_benign",
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"acmg_by_gene": [
{
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"criteria": [
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"BP4_Strong",
"BP7"
],
"verdict": "Likely_benign",
"transcript": "ENST00000376087.5",
"gene_symbol": "ANKRD26",
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"effects": [
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"inheritance_mode": "AD",
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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
}