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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: 15-78168952-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=78168952&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "15",
"pos": 78168952,
"ref": "A",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_005530.3",
"consequences": [
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "c.1048A>G",
"hgvs_p": "p.Lys350Glu",
"transcript": "NM_005530.3",
"protein_id": "NP_005521.1",
"transcript_support_level": null,
"aa_start": 350,
"aa_end": null,
"aa_length": 366,
"cds_start": 1048,
"cds_end": null,
"cds_length": 1101,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000299518.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_005530.3"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "c.1048A>G",
"hgvs_p": "p.Lys350Glu",
"transcript": "ENST00000299518.7",
"protein_id": "ENSP00000299518.2",
"transcript_support_level": 1,
"aa_start": 350,
"aa_end": null,
"aa_length": 366,
"cds_start": 1048,
"cds_end": null,
"cds_length": 1101,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_005530.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000299518.7"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ACSBG1",
"gene_hgnc_id": 29567,
"hgvs_c": "c.*2492T>C",
"hgvs_p": null,
"transcript": "NM_015162.5",
"protein_id": "NP_055977.3",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 724,
"cds_start": null,
"cds_end": null,
"cds_length": 2175,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000258873.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_015162.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ACSBG1",
"gene_hgnc_id": 29567,
"hgvs_c": "c.*2492T>C",
"hgvs_p": null,
"transcript": "ENST00000258873.9",
"protein_id": "ENSP00000258873.4",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 724,
"cds_start": null,
"cds_end": null,
"cds_length": 2175,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_015162.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000258873.9"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "n.996A>G",
"hgvs_p": null,
"transcript": "ENST00000558535.1",
"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": "pseudogene",
"feature": "ENST00000558535.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "n.1739A>G",
"hgvs_p": null,
"transcript": "ENST00000559889.5",
"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": "ENST00000559889.5"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "c.1072A>G",
"hgvs_p": "p.Lys358Glu",
"transcript": "ENST00000889878.1",
"protein_id": "ENSP00000559937.1",
"transcript_support_level": null,
"aa_start": 358,
"aa_end": null,
"aa_length": 374,
"cds_start": 1072,
"cds_end": null,
"cds_length": 1125,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000889878.1"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "c.1069A>G",
"hgvs_p": "p.Lys357Glu",
"transcript": "ENST00000889873.1",
"protein_id": "ENSP00000559932.1",
"transcript_support_level": null,
"aa_start": 357,
"aa_end": null,
"aa_length": 373,
"cds_start": 1069,
"cds_end": null,
"cds_length": 1122,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000889873.1"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "c.1045A>G",
"hgvs_p": "p.Lys349Glu",
"transcript": "ENST00000889876.1",
"protein_id": "ENSP00000559935.1",
"transcript_support_level": null,
"aa_start": 349,
"aa_end": null,
"aa_length": 365,
"cds_start": 1045,
"cds_end": null,
"cds_length": 1098,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000889876.1"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "c.1045A>G",
"hgvs_p": "p.Lys349Glu",
"transcript": "ENST00000921734.1",
"protein_id": "ENSP00000591793.1",
"transcript_support_level": null,
"aa_start": 349,
"aa_end": null,
"aa_length": 365,
"cds_start": 1045,
"cds_end": null,
"cds_length": 1098,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000921734.1"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "c.1024A>G",
"hgvs_p": "p.Lys342Glu",
"transcript": "ENST00000889871.1",
"protein_id": "ENSP00000559930.1",
"transcript_support_level": null,
"aa_start": 342,
"aa_end": null,
"aa_length": 358,
"cds_start": 1024,
"cds_end": null,
"cds_length": 1077,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000889871.1"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "c.1012A>G",
"hgvs_p": "p.Lys338Glu",
"transcript": "ENST00000889872.1",
"protein_id": "ENSP00000559931.1",
"transcript_support_level": null,
"aa_start": 338,
"aa_end": null,
"aa_length": 354,
"cds_start": 1012,
"cds_end": null,
"cds_length": 1065,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000889872.1"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "c.988A>G",
"hgvs_p": "p.Lys330Glu",
"transcript": "ENST00000943584.1",
"protein_id": "ENSP00000613643.1",
"transcript_support_level": null,
"aa_start": 330,
"aa_end": null,
"aa_length": 346,
"cds_start": 988,
"cds_end": null,
"cds_length": 1041,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000943584.1"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "c.985A>G",
"hgvs_p": "p.Lys329Glu",
"transcript": "ENST00000889877.1",
"protein_id": "ENSP00000559936.1",
"transcript_support_level": null,
"aa_start": 329,
"aa_end": null,
"aa_length": 345,
"cds_start": 985,
"cds_end": null,
"cds_length": 1038,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000889877.1"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "c.943A>G",
"hgvs_p": "p.Lys315Glu",
"transcript": "ENST00000558554.5",
"protein_id": "ENSP00000453084.1",
"transcript_support_level": 2,
"aa_start": 315,
"aa_end": null,
"aa_length": 331,
"cds_start": 943,
"cds_end": null,
"cds_length": 996,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000558554.5"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "c.901A>G",
"hgvs_p": "p.Lys301Glu",
"transcript": "ENST00000889874.1",
"protein_id": "ENSP00000559933.1",
"transcript_support_level": null,
"aa_start": 301,
"aa_end": null,
"aa_length": 317,
"cds_start": 901,
"cds_end": null,
"cds_length": 954,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000889874.1"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "c.895A>G",
"hgvs_p": "p.Lys299Glu",
"transcript": "ENST00000889875.1",
"protein_id": "ENSP00000559934.1",
"transcript_support_level": null,
"aa_start": 299,
"aa_end": null,
"aa_length": 315,
"cds_start": 895,
"cds_end": null,
"cds_length": 948,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000889875.1"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "c.211A>G",
"hgvs_p": "p.Lys71Glu",
"transcript": "ENST00000559205.1",
"protein_id": "ENSP00000453989.1",
"transcript_support_level": 4,
"aa_start": 71,
"aa_end": null,
"aa_length": 87,
"cds_start": 211,
"cds_end": null,
"cds_length": 264,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000559205.1"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "c.898A>G",
"hgvs_p": "p.Lys300Glu",
"transcript": "XM_024449911.2",
"protein_id": "XP_024305679.1",
"transcript_support_level": null,
"aa_start": 300,
"aa_end": null,
"aa_length": 316,
"cds_start": 898,
"cds_end": null,
"cds_length": 951,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_024449911.2"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "c.898A>G",
"hgvs_p": "p.Lys300Glu",
"transcript": "XM_047432428.1",
"protein_id": "XP_047288384.1",
"transcript_support_level": null,
"aa_start": 300,
"aa_end": null,
"aa_length": 316,
"cds_start": 898,
"cds_end": null,
"cds_length": 951,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047432428.1"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "c.898A>G",
"hgvs_p": "p.Lys300Glu",
"transcript": "XM_047432429.1",
"protein_id": "XP_047288385.1",
"transcript_support_level": null,
"aa_start": 300,
"aa_end": null,
"aa_length": 316,
"cds_start": 898,
"cds_end": null,
"cds_length": 951,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047432429.1"
},
{
"aa_ref": "K",
"aa_alt": "E",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IDH3A",
"gene_hgnc_id": 5384,
"hgvs_c": "c.721A>G",
"hgvs_p": "p.Lys241Glu",
"transcript": "XM_047432430.1",
"protein_id": "XP_047288386.1",
"transcript_support_level": null,
"aa_start": 241,
"aa_end": null,
"aa_length": 257,
"cds_start": 721,
"cds_end": null,
"cds_length": 774,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
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"feature": "XM_011521390.4"
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{
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{
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{
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"protein_coding": false,
"strand": true,
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],
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"gene_symbol": "IDH3A",
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"transcript": "ENST00000557960.1",
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{
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"strand": true,
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{
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"strand": true,
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{
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{
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{
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{
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"feature": "ENST00000560667.5"
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],
"gene_symbol": "IDH3A",
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"dbsnp": "rs2141308114",
"frequency_reference_population": 0.0000013775547,
"hom_count_reference_population": 0,
"allele_count_reference_population": 2,
"gnomad_exomes_af": 0.00000137755,
"gnomad_genomes_af": null,
"gnomad_exomes_ac": 2,
"gnomad_genomes_ac": null,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": null,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.4581112861633301,
"computational_prediction_selected": "Uncertain_significance",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.029999999329447746,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.285,
"revel_prediction": "Benign",
"alphamissense_score": 0.4363,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.04,
"bayesdelnoaf_prediction": "Uncertain_significance",
"phylop100way_score": 6.431,
"phylop100way_prediction": "Uncertain_significance",
"spliceai_max_score": 0.03,
"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_005530.3",
"gene_symbol": "IDH3A",
"hgnc_id": 5384,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.1048A>G",
"hgvs_p": "p.Lys350Glu"
},
{
"score": 2,
"benign_score": 0,
"pathogenic_score": 2,
"criteria": [
"PM2"
],
"verdict": "Uncertain_significance",
"transcript": "NM_015162.5",
"gene_symbol": "ACSBG1",
"hgnc_id": 29567,
"effects": [
"3_prime_UTR_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.*2492T>C",
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}
],
"clinvar_disease": "not provided,not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "US:2",
"phenotype_combined": "not provided|not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}