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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: 6-155257108-A-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=155257108&ref=A&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "6",
"pos": 155257108,
"ref": "A",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_012454.4",
"consequences": [
{
"aa_ref": "H",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIAM2",
"gene_hgnc_id": 11806,
"hgvs_c": "c.5093A>T",
"hgvs_p": "p.His1698Leu",
"transcript": "NM_012454.4",
"protein_id": "NP_036586.3",
"transcript_support_level": null,
"aa_start": 1698,
"aa_end": null,
"aa_length": 1701,
"cds_start": 5093,
"cds_end": null,
"cds_length": 5106,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000682666.1",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_012454.4"
},
{
"aa_ref": "H",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIAM2",
"gene_hgnc_id": 11806,
"hgvs_c": "c.5093A>T",
"hgvs_p": "p.His1698Leu",
"transcript": "ENST00000682666.1",
"protein_id": "ENSP00000507157.1",
"transcript_support_level": null,
"aa_start": 1698,
"aa_end": null,
"aa_length": 1701,
"cds_start": 5093,
"cds_end": null,
"cds_length": 5106,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_012454.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000682666.1"
},
{
"aa_ref": "H",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIAM2",
"gene_hgnc_id": 11806,
"hgvs_c": "c.3029A>T",
"hgvs_p": "p.His1010Leu",
"transcript": "ENST00000456877.6",
"protein_id": "ENSP00000407183.2",
"transcript_support_level": 1,
"aa_start": 1010,
"aa_end": null,
"aa_length": 1013,
"cds_start": 3029,
"cds_end": null,
"cds_length": 3042,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000456877.6"
},
{
"aa_ref": "H",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIAM2",
"gene_hgnc_id": 11806,
"hgvs_c": "c.1868A>T",
"hgvs_p": "p.His623Leu",
"transcript": "ENST00000275246.11",
"protein_id": "ENSP00000275246.7",
"transcript_support_level": 1,
"aa_start": 623,
"aa_end": null,
"aa_length": 626,
"cds_start": 1868,
"cds_end": null,
"cds_length": 1881,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000275246.11"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TFB1M",
"gene_hgnc_id": 17037,
"hgvs_c": "c.*728T>A",
"hgvs_p": null,
"transcript": "NM_016020.4",
"protein_id": "NP_057104.2",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 346,
"cds_start": null,
"cds_end": null,
"cds_length": 1041,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000367166.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_016020.4"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TFB1M",
"gene_hgnc_id": 17037,
"hgvs_c": "c.*728T>A",
"hgvs_p": null,
"transcript": "ENST00000367166.5",
"protein_id": "ENSP00000356134.4",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 346,
"cds_start": null,
"cds_end": null,
"cds_length": 1041,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_016020.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000367166.5"
},
{
"aa_ref": "H",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIAM2",
"gene_hgnc_id": 11806,
"hgvs_c": "c.5252A>T",
"hgvs_p": "p.His1751Leu",
"transcript": "ENST00000950126.1",
"protein_id": "ENSP00000620185.1",
"transcript_support_level": null,
"aa_start": 1751,
"aa_end": null,
"aa_length": 1754,
"cds_start": 5252,
"cds_end": null,
"cds_length": 5265,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000950126.1"
},
{
"aa_ref": "H",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIAM2",
"gene_hgnc_id": 11806,
"hgvs_c": "c.5180A>T",
"hgvs_p": "p.His1727Leu",
"transcript": "ENST00000529824.6",
"protein_id": "ENSP00000433348.2",
"transcript_support_level": 5,
"aa_start": 1727,
"aa_end": null,
"aa_length": 1730,
"cds_start": 5180,
"cds_end": null,
"cds_length": 5193,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000529824.6"
},
{
"aa_ref": "H",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIAM2",
"gene_hgnc_id": 11806,
"hgvs_c": "c.5165A>T",
"hgvs_p": "p.His1722Leu",
"transcript": "ENST00000360366.8",
"protein_id": "ENSP00000353528.4",
"transcript_support_level": 5,
"aa_start": 1722,
"aa_end": null,
"aa_length": 1725,
"cds_start": 5165,
"cds_end": null,
"cds_length": 5178,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000360366.8"
},
{
"aa_ref": "H",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIAM2",
"gene_hgnc_id": 11806,
"hgvs_c": "c.5093A>T",
"hgvs_p": "p.His1698Leu",
"transcript": "NM_001384546.1",
"protein_id": "NP_001371475.1",
"transcript_support_level": null,
"aa_start": 1698,
"aa_end": null,
"aa_length": 1701,
"cds_start": 5093,
"cds_end": null,
"cds_length": 5106,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001384546.1"
},
{
"aa_ref": "H",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIAM2",
"gene_hgnc_id": 11806,
"hgvs_c": "c.5093A>T",
"hgvs_p": "p.His1698Leu",
"transcript": "NM_001384547.1",
"protein_id": "NP_001371476.1",
"transcript_support_level": null,
"aa_start": 1698,
"aa_end": null,
"aa_length": 1701,
"cds_start": 5093,
"cds_end": null,
"cds_length": 5106,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001384547.1"
},
{
"aa_ref": "H",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 29,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIAM2",
"gene_hgnc_id": 11806,
"hgvs_c": "c.5093A>T",
"hgvs_p": "p.His1698Leu",
"transcript": "ENST00000461783.7",
"protein_id": "ENSP00000437188.2",
"transcript_support_level": 2,
"aa_start": 1698,
"aa_end": null,
"aa_length": 1701,
"cds_start": 5093,
"cds_end": null,
"cds_length": 5106,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000461783.7"
},
{
"aa_ref": "H",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIAM2",
"gene_hgnc_id": 11806,
"hgvs_c": "c.5093A>T",
"hgvs_p": "p.His1698Leu",
"transcript": "ENST00000929431.1",
"protein_id": "ENSP00000599490.1",
"transcript_support_level": null,
"aa_start": 1698,
"aa_end": null,
"aa_length": 1701,
"cds_start": 5093,
"cds_end": null,
"cds_length": 5106,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000929431.1"
},
{
"aa_ref": "H",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIAM2",
"gene_hgnc_id": 11806,
"hgvs_c": "c.5093A>T",
"hgvs_p": "p.His1698Leu",
"transcript": "ENST00000950123.1",
"protein_id": "ENSP00000620182.1",
"transcript_support_level": null,
"aa_start": 1698,
"aa_end": null,
"aa_length": 1701,
"cds_start": 5093,
"cds_end": null,
"cds_length": 5106,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000950123.1"
},
{
"aa_ref": "H",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIAM2",
"gene_hgnc_id": 11806,
"hgvs_c": "c.5093A>T",
"hgvs_p": "p.His1698Leu",
"transcript": "ENST00000950124.1",
"protein_id": "ENSP00000620183.1",
"transcript_support_level": null,
"aa_start": 1698,
"aa_end": null,
"aa_length": 1701,
"cds_start": 5093,
"cds_end": null,
"cds_length": 5106,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000950124.1"
},
{
"aa_ref": "H",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIAM2",
"gene_hgnc_id": 11806,
"hgvs_c": "c.5093A>T",
"hgvs_p": "p.His1698Leu",
"transcript": "ENST00000950125.1",
"protein_id": "ENSP00000620184.1",
"transcript_support_level": null,
"aa_start": 1698,
"aa_end": null,
"aa_length": 1701,
"cds_start": 5093,
"cds_end": null,
"cds_length": 5106,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000950125.1"
},
{
"aa_ref": "H",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIAM2",
"gene_hgnc_id": 11806,
"hgvs_c": "c.3125A>T",
"hgvs_p": "p.His1042Leu",
"transcript": "ENST00000528391.6",
"protein_id": "ENSP00000435335.2",
"transcript_support_level": 2,
"aa_start": 1042,
"aa_end": null,
"aa_length": 1045,
"cds_start": 3125,
"cds_end": null,
"cds_length": 3138,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000528391.6"
},
{
"aa_ref": "H",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TIAM2",
"gene_hgnc_id": 11806,
"hgvs_c": "c.1868A>T",
"hgvs_p": "p.His623Leu",
"transcript": "NM_001010927.3",
"protein_id": "NP_001010927.2",
"transcript_support_level": null,
"aa_start": 623,
"aa_end": null,
"aa_length": 626,
"cds_start": 1868,
"cds_end": null,
"cds_length": 1881,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001010927.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TFB1M",
"gene_hgnc_id": 17037,
"hgvs_c": "c.*728T>A",
"hgvs_p": null,
"transcript": "NM_001350501.2",
"protein_id": "NP_001337430.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 288,
"cds_start": null,
"cds_end": null,
"cds_length": 867,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001350501.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TFB1M",
"gene_hgnc_id": 17037,
"hgvs_c": "c.*728T>A",
"hgvs_p": null,
"transcript": "NM_001350502.2",
"protein_id": "NP_001337431.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 251,
"cds_start": null,
"cds_end": null,
"cds_length": 756,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001350502.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "TFB1M",
"gene_hgnc_id": 17037,
"hgvs_c": "c.*728T>A",
"hgvs_p": null,
"transcript": "XM_011535873.3",
"protein_id": "XP_011534175.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 251,
"cds_start": null,
"cds_end": null,
"cds_length": 756,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011535873.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "TFB1M",
"gene_hgnc_id": 17037,
"hgvs_c": "c.667-3344T>A",
"hgvs_p": null,
"transcript": "XM_011535871.3",
"protein_id": "XP_011534173.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 267,
"cds_start": null,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
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"cdna_length": null,
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"biotype": "protein_coding",
"feature": "XM_011535871.3"
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 5,
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"gene_symbol": "TFB1M",
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"hgvs_c": "c.667-3344T>A",
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"transcript": "XM_011535872.3",
"protein_id": "XP_011534174.1",
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"aa_start": null,
"aa_end": null,
"aa_length": 267,
"cds_start": null,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
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"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011535872.3"
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 5,
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"gene_symbol": "TFB1M",
"gene_hgnc_id": 17037,
"hgvs_c": "c.667-3344T>A",
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"transcript": "XM_047418852.1",
"protein_id": "XP_047274808.1",
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"aa_start": null,
"aa_end": null,
"aa_length": 267,
"cds_start": null,
"cds_end": null,
"cds_length": 804,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047418852.1"
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 9,
"intron_rank": 5,
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"gene_symbol": "TFB1M",
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"hgvs_c": "n.723-3344T>A",
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"transcript": "NR_146725.2",
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "NR_146725.2"
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
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"exon_count": 8,
"intron_rank": 5,
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"gene_symbol": "TFB1M",
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"hgvs_c": "n.723-3344T>A",
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"transcript": "XR_007059269.1",
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"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "XR_007059269.1"
}
],
"gene_symbol": "TIAM2",
"gene_hgnc_id": 11806,
"dbsnp": "rs199608026",
"frequency_reference_population": 0.000021693399,
"hom_count_reference_population": 0,
"allele_count_reference_population": 35,
"gnomad_exomes_af": 0.0000191557,
"gnomad_genomes_af": 0.000046148,
"gnomad_exomes_ac": 28,
"gnomad_genomes_ac": 7,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.018265992403030396,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.156,
"revel_prediction": "Benign",
"alphamissense_score": 0.093,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.23,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 2.45,
"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": -4,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Strong",
"acmg_by_gene": [
{
"score": -4,
"benign_score": 4,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "NM_012454.4",
"gene_symbol": "TIAM2",
"hgnc_id": 11806,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.5093A>T",
"hgvs_p": "p.His1698Leu"
},
{
"score": -4,
"benign_score": 4,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "NM_016020.4",
"gene_symbol": "TFB1M",
"hgnc_id": 17037,
"effects": [
"3_prime_UTR_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.*728T>A",
"hgvs_p": null
}
],
"clinvar_disease": "not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}