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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: 16-75234923-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=75234923&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "16",
"pos": 75234923,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_001170714.3",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.1976G>C",
"hgvs_p": "p.Gly659Ala",
"transcript": "NM_014567.5",
"protein_id": "NP_055382.2",
"transcript_support_level": null,
"aa_start": 659,
"aa_end": null,
"aa_length": 870,
"cds_start": 1976,
"cds_end": null,
"cds_length": 2613,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000162330.10",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_014567.5"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.1976G>C",
"hgvs_p": "p.Gly659Ala",
"transcript": "ENST00000162330.10",
"protein_id": "ENSP00000162330.5",
"transcript_support_level": 1,
"aa_start": 659,
"aa_end": null,
"aa_length": 870,
"cds_start": 1976,
"cds_end": null,
"cds_length": 2613,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_014567.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000162330.10"
},
{
"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": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "n.1581G>C",
"hgvs_p": null,
"transcript": "ENST00000563038.5",
"protein_id": null,
"transcript_support_level": 1,
"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": "retained_intron",
"feature": "ENST00000563038.5"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.2114G>C",
"hgvs_p": "p.Gly705Ala",
"transcript": "NM_001170714.3",
"protein_id": "NP_001164185.1",
"transcript_support_level": null,
"aa_start": 705,
"aa_end": null,
"aa_length": 916,
"cds_start": 2114,
"cds_end": null,
"cds_length": 2751,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001170714.3"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.2114G>C",
"hgvs_p": "p.Gly705Ala",
"transcript": "ENST00000418647.7",
"protein_id": "ENSP00000391669.3",
"transcript_support_level": 2,
"aa_start": 705,
"aa_end": null,
"aa_length": 916,
"cds_start": 2114,
"cds_end": null,
"cds_length": 2751,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000418647.7"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.1976G>C",
"hgvs_p": "p.Gly659Ala",
"transcript": "ENST00000853597.1",
"protein_id": "ENSP00000523656.1",
"transcript_support_level": null,
"aa_start": 659,
"aa_end": null,
"aa_length": 891,
"cds_start": 1976,
"cds_end": null,
"cds_length": 2676,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000853597.1"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.2030G>C",
"hgvs_p": "p.Gly677Ala",
"transcript": "NM_001170715.3",
"protein_id": "NP_001164186.1",
"transcript_support_level": null,
"aa_start": 677,
"aa_end": null,
"aa_length": 888,
"cds_start": 2030,
"cds_end": null,
"cds_length": 2667,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001170715.3"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.2030G>C",
"hgvs_p": "p.Gly677Ala",
"transcript": "NM_001170716.3",
"protein_id": "NP_001164187.1",
"transcript_support_level": null,
"aa_start": 677,
"aa_end": null,
"aa_length": 888,
"cds_start": 2030,
"cds_end": null,
"cds_length": 2667,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001170716.3"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.2030G>C",
"hgvs_p": "p.Gly677Ala",
"transcript": "NM_001170717.3",
"protein_id": "NP_001164188.1",
"transcript_support_level": null,
"aa_start": 677,
"aa_end": null,
"aa_length": 888,
"cds_start": 2030,
"cds_end": null,
"cds_length": 2667,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001170717.3"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.2030G>C",
"hgvs_p": "p.Gly677Ala",
"transcript": "ENST00000393420.10",
"protein_id": "ENSP00000377072.6",
"transcript_support_level": 5,
"aa_start": 677,
"aa_end": null,
"aa_length": 888,
"cds_start": 2030,
"cds_end": null,
"cds_length": 2667,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000393420.10"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.2030G>C",
"hgvs_p": "p.Gly677Ala",
"transcript": "ENST00000393422.6",
"protein_id": "ENSP00000377074.2",
"transcript_support_level": 2,
"aa_start": 677,
"aa_end": null,
"aa_length": 888,
"cds_start": 2030,
"cds_end": null,
"cds_length": 2667,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000393422.6"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.2030G>C",
"hgvs_p": "p.Gly677Ala",
"transcript": "ENST00000420641.7",
"protein_id": "ENSP00000392708.3",
"transcript_support_level": 2,
"aa_start": 677,
"aa_end": null,
"aa_length": 888,
"cds_start": 2030,
"cds_end": null,
"cds_length": 2667,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000420641.7"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.1994G>C",
"hgvs_p": "p.Gly665Ala",
"transcript": "ENST00000942293.1",
"protein_id": "ENSP00000612352.1",
"transcript_support_level": null,
"aa_start": 665,
"aa_end": null,
"aa_length": 876,
"cds_start": 1994,
"cds_end": null,
"cds_length": 2631,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942293.1"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.1976G>C",
"hgvs_p": "p.Gly659Ala",
"transcript": "NM_001170718.3",
"protein_id": "NP_001164189.1",
"transcript_support_level": null,
"aa_start": 659,
"aa_end": null,
"aa_length": 870,
"cds_start": 1976,
"cds_end": null,
"cds_length": 2613,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001170718.3"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.1976G>C",
"hgvs_p": "p.Gly659Ala",
"transcript": "ENST00000538440.6",
"protein_id": "ENSP00000443841.2",
"transcript_support_level": 2,
"aa_start": 659,
"aa_end": null,
"aa_length": 870,
"cds_start": 1976,
"cds_end": null,
"cds_length": 2613,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000538440.6"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.1970G>C",
"hgvs_p": "p.Gly657Ala",
"transcript": "NM_001170719.3",
"protein_id": "NP_001164190.1",
"transcript_support_level": null,
"aa_start": 657,
"aa_end": null,
"aa_length": 868,
"cds_start": 1970,
"cds_end": null,
"cds_length": 2607,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001170719.3"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.1970G>C",
"hgvs_p": "p.Gly657Ala",
"transcript": "ENST00000542031.6",
"protein_id": "ENSP00000440415.2",
"transcript_support_level": 2,
"aa_start": 657,
"aa_end": null,
"aa_length": 868,
"cds_start": 1970,
"cds_end": null,
"cds_length": 2607,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000542031.6"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.1976G>C",
"hgvs_p": "p.Gly659Ala",
"transcript": "ENST00000928349.1",
"protein_id": "ENSP00000598408.1",
"transcript_support_level": null,
"aa_start": 659,
"aa_end": null,
"aa_length": 868,
"cds_start": 1976,
"cds_end": null,
"cds_length": 2607,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000928349.1"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.1976G>C",
"hgvs_p": "p.Gly659Ala",
"transcript": "ENST00000942295.1",
"protein_id": "ENSP00000612354.1",
"transcript_support_level": null,
"aa_start": 659,
"aa_end": null,
"aa_length": 867,
"cds_start": 1976,
"cds_end": null,
"cds_length": 2604,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942295.1"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.1883G>C",
"hgvs_p": "p.Gly628Ala",
"transcript": "ENST00000942294.1",
"protein_id": "ENSP00000612353.1",
"transcript_support_level": null,
"aa_start": 628,
"aa_end": null,
"aa_length": 839,
"cds_start": 1883,
"cds_end": null,
"cds_length": 2520,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942294.1"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.1697G>C",
"hgvs_p": "p.Gly566Ala",
"transcript": "ENST00000853596.1",
"protein_id": "ENSP00000523655.1",
"transcript_support_level": null,
"aa_start": 566,
"aa_end": null,
"aa_length": 777,
"cds_start": 1697,
"cds_end": null,
"cds_length": 2334,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000853596.1"
},
{
"aa_ref": "G",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"hgvs_c": "c.1532G>C",
"hgvs_p": "p.Gly511Ala",
"transcript": "NM_001170720.3",
"protein_id": "NP_001164191.1",
"transcript_support_level": null,
"aa_start": 511,
"aa_end": null,
"aa_length": 722,
"cds_start": 1532,
"cds_end": null,
"cds_length": 2169,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
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{
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{
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{
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},
{
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"gene_symbol": "BCAR1",
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},
{
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],
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},
{
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],
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{
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],
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"biotype": "pseudogene",
"feature": "ENST00000566982.1"
},
{
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
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"gene_symbol": "BCAR1",
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"transcript": "ENST00000562556.5",
"protein_id": "ENSP00000455166.1",
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"cds_start": null,
"cds_end": null,
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"cdna_start": null,
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"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000562556.5"
}
],
"gene_symbol": "BCAR1",
"gene_hgnc_id": 971,
"dbsnp": "rs1232194704",
"frequency_reference_population": 7.1379526e-7,
"hom_count_reference_population": 0,
"allele_count_reference_population": 1,
"gnomad_exomes_af": 7.13795e-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": 0.46471476554870605,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.177,
"revel_prediction": "Benign",
"alphamissense_score": 0.1595,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.17,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 5.841,
"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": 2,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2",
"acmg_by_gene": [
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "NM_001170714.3",
"gene_symbol": "BCAR1",
"hgnc_id": 971,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.2114G>C",
"hgvs_p": "p.Gly705Ala"
}
],
"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
}