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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: 16-84408489-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=84408489&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "16",
"pos": 84408489,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001286527.3",
"consequences": [
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.412G>A",
"hgvs_p": "p.Ala138Thr",
"transcript": "NM_014861.4",
"protein_id": "NP_055676.3",
"transcript_support_level": null,
"aa_start": 138,
"aa_end": null,
"aa_length": 946,
"cds_start": 412,
"cds_end": null,
"cds_length": 2841,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000262429.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_014861.4"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.412G>A",
"hgvs_p": "p.Ala138Thr",
"transcript": "ENST00000262429.9",
"protein_id": "ENSP00000262429.4",
"transcript_support_level": 1,
"aa_start": 138,
"aa_end": null,
"aa_length": 946,
"cds_start": 412,
"cds_end": null,
"cds_length": 2841,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_014861.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000262429.9"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.412G>A",
"hgvs_p": "p.Ala138Thr",
"transcript": "ENST00000416219.7",
"protein_id": "ENSP00000397925.2",
"transcript_support_level": 1,
"aa_start": 138,
"aa_end": null,
"aa_length": 975,
"cds_start": 412,
"cds_end": null,
"cds_length": 2928,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000416219.7"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.412G>A",
"hgvs_p": "p.Ala138Thr",
"transcript": "NM_001286527.3",
"protein_id": "NP_001273456.2",
"transcript_support_level": null,
"aa_start": 138,
"aa_end": null,
"aa_length": 975,
"cds_start": 412,
"cds_end": null,
"cds_length": 2928,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001286527.3"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.412G>A",
"hgvs_p": "p.Ala138Thr",
"transcript": "ENST00000861763.1",
"protein_id": "ENSP00000531822.1",
"transcript_support_level": null,
"aa_start": 138,
"aa_end": null,
"aa_length": 971,
"cds_start": 412,
"cds_end": null,
"cds_length": 2916,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000861763.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.412G>A",
"hgvs_p": "p.Ala138Thr",
"transcript": "ENST00000861768.1",
"protein_id": "ENSP00000531827.1",
"transcript_support_level": null,
"aa_start": 138,
"aa_end": null,
"aa_length": 971,
"cds_start": 412,
"cds_end": null,
"cds_length": 2916,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000861768.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.346G>A",
"hgvs_p": "p.Ala116Thr",
"transcript": "ENST00000861767.1",
"protein_id": "ENSP00000531826.1",
"transcript_support_level": null,
"aa_start": 116,
"aa_end": null,
"aa_length": 952,
"cds_start": 346,
"cds_end": null,
"cds_length": 2859,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000861767.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.406G>A",
"hgvs_p": "p.Ala136Thr",
"transcript": "ENST00000861766.1",
"protein_id": "ENSP00000531825.1",
"transcript_support_level": null,
"aa_start": 136,
"aa_end": null,
"aa_length": 944,
"cds_start": 406,
"cds_end": null,
"cds_length": 2835,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000861766.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.412G>A",
"hgvs_p": "p.Ala138Thr",
"transcript": "ENST00000957789.1",
"protein_id": "ENSP00000627848.1",
"transcript_support_level": null,
"aa_start": 138,
"aa_end": null,
"aa_length": 944,
"cds_start": 412,
"cds_end": null,
"cds_length": 2835,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000957789.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.412G>A",
"hgvs_p": "p.Ala138Thr",
"transcript": "ENST00000861764.1",
"protein_id": "ENSP00000531823.1",
"transcript_support_level": null,
"aa_start": 138,
"aa_end": null,
"aa_length": 943,
"cds_start": 412,
"cds_end": null,
"cds_length": 2832,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000861764.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.412G>A",
"hgvs_p": "p.Ala138Thr",
"transcript": "ENST00000861771.1",
"protein_id": "ENSP00000531830.1",
"transcript_support_level": null,
"aa_start": 138,
"aa_end": null,
"aa_length": 942,
"cds_start": 412,
"cds_end": null,
"cds_length": 2829,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000861771.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.412G>A",
"hgvs_p": "p.Ala138Thr",
"transcript": "ENST00000957791.1",
"protein_id": "ENSP00000627850.1",
"transcript_support_level": null,
"aa_start": 138,
"aa_end": null,
"aa_length": 941,
"cds_start": 412,
"cds_end": null,
"cds_length": 2826,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000957791.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.412G>A",
"hgvs_p": "p.Ala138Thr",
"transcript": "ENST00000861762.1",
"protein_id": "ENSP00000531821.1",
"transcript_support_level": null,
"aa_start": 138,
"aa_end": null,
"aa_length": 912,
"cds_start": 412,
"cds_end": null,
"cds_length": 2739,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000861762.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.301G>A",
"hgvs_p": "p.Ala101Thr",
"transcript": "ENST00000957790.1",
"protein_id": "ENSP00000627849.1",
"transcript_support_level": null,
"aa_start": 101,
"aa_end": null,
"aa_length": 909,
"cds_start": 301,
"cds_end": null,
"cds_length": 2730,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000957790.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.412G>A",
"hgvs_p": "p.Ala138Thr",
"transcript": "ENST00000861769.1",
"protein_id": "ENSP00000531828.1",
"transcript_support_level": null,
"aa_start": 138,
"aa_end": null,
"aa_length": 907,
"cds_start": 412,
"cds_end": null,
"cds_length": 2724,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000861769.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.412G>A",
"hgvs_p": "p.Ala138Thr",
"transcript": "ENST00000861770.1",
"protein_id": "ENSP00000531829.1",
"transcript_support_level": null,
"aa_start": 138,
"aa_end": null,
"aa_length": 889,
"cds_start": 412,
"cds_end": null,
"cds_length": 2670,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000861770.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.412G>A",
"hgvs_p": "p.Ala138Thr",
"transcript": "ENST00000861765.1",
"protein_id": "ENSP00000531824.1",
"transcript_support_level": null,
"aa_start": 138,
"aa_end": null,
"aa_length": 873,
"cds_start": 412,
"cds_end": null,
"cds_length": 2622,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000861765.1"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.343G>A",
"hgvs_p": "p.Ala115Thr",
"transcript": "XM_011523486.3",
"protein_id": "XP_011521788.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 952,
"cds_start": 343,
"cds_end": null,
"cds_length": 2859,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011523486.3"
},
{
"aa_ref": "A",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.343G>A",
"hgvs_p": "p.Ala115Thr",
"transcript": "XM_047434994.1",
"protein_id": "XP_047290950.1",
"transcript_support_level": null,
"aa_start": 115,
"aa_end": null,
"aa_length": 923,
"cds_start": 343,
"cds_end": null,
"cds_length": 2772,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047434994.1"
},
{
"aa_ref": "S",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"synonymous_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "c.21G>A",
"hgvs_p": "p.Ser7Ser",
"transcript": "NM_001291454.2",
"protein_id": "NP_001278383.1",
"transcript_support_level": null,
"aa_start": 7,
"aa_end": null,
"aa_length": 795,
"cds_start": 21,
"cds_end": null,
"cds_length": 2388,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001291454.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "n.147G>A",
"hgvs_p": null,
"transcript": "ENST00000420010.6",
"protein_id": null,
"transcript_support_level": 2,
"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": "ENST00000420010.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "n.147G>A",
"hgvs_p": null,
"transcript": "ENST00000565546.5",
"protein_id": null,
"transcript_support_level": 5,
"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": "ENST00000565546.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "n.903G>A",
"hgvs_p": null,
"transcript": "ENST00000565631.5",
"protein_id": null,
"transcript_support_level": 2,
"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": "ENST00000565631.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "n.401G>A",
"hgvs_p": null,
"transcript": "ENST00000565927.1",
"protein_id": null,
"transcript_support_level": 4,
"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": "ENST00000565927.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "n.52G>A",
"hgvs_p": null,
"transcript": "ENST00000568160.1",
"protein_id": null,
"transcript_support_level": 3,
"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": "ENST00000568160.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"hgvs_c": "n.109G>A",
"hgvs_p": null,
"transcript": "ENST00000569207.5",
"protein_id": "ENSP00000456595.1",
"transcript_support_level": 5,
"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": "nonsense_mediated_decay",
"feature": "ENST00000569207.5"
}
],
"gene_symbol": "ATP2C2",
"gene_hgnc_id": 29103,
"dbsnp": "rs78371901",
"frequency_reference_population": 0.00381161,
"hom_count_reference_population": 31,
"allele_count_reference_population": 6146,
"gnomad_exomes_af": 0.0038365,
"gnomad_genomes_af": 0.00357246,
"gnomad_exomes_ac": 5603,
"gnomad_genomes_ac": 543,
"gnomad_exomes_homalt": 28,
"gnomad_genomes_homalt": 3,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.009264618158340454,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.333,
"revel_prediction": "Uncertain_significance",
"alphamissense_score": 0.0769,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.25,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.24,
"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": -20,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS1,BS2",
"acmg_by_gene": [
{
"score": -20,
"benign_score": 20,
"pathogenic_score": 0,
"criteria": [
"BP4_Strong",
"BP6_Very_Strong",
"BS1",
"BS2"
],
"verdict": "Benign",
"transcript": "NM_001286527.3",
"gene_symbol": "ATP2C2",
"hgnc_id": 29103,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.412G>A",
"hgvs_p": "p.Ala138Thr"
}
],
"clinvar_disease": "not provided",
"clinvar_classification": "Benign",
"clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
"clinvar_submissions_summary": "B:2",
"phenotype_combined": "not provided",
"pathogenicity_classification_combined": "Benign",
"custom_annotations": null
}
],
"message": null
}