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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: 1-145897026-T-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=145897026&ref=T&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 145897026,
"ref": "T",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_003637.5",
"consequences": [
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2729A>T",
"hgvs_p": "p.Lys910Met",
"transcript": "NM_003637.5",
"protein_id": "NP_003628.2",
"transcript_support_level": null,
"aa_start": 910,
"aa_end": null,
"aa_length": 1167,
"cds_start": 2729,
"cds_end": null,
"cds_length": 3504,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000369304.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_003637.5"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2729A>T",
"hgvs_p": "p.Lys910Met",
"transcript": "ENST00000369304.8",
"protein_id": "ENSP00000358310.3",
"transcript_support_level": 1,
"aa_start": 910,
"aa_end": null,
"aa_length": 1167,
"cds_start": 2729,
"cds_end": null,
"cds_length": 3504,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_003637.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000369304.8"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2300A>T",
"hgvs_p": "p.Lys767Met",
"transcript": "ENST00000539363.2",
"protein_id": "ENSP00000439894.1",
"transcript_support_level": 1,
"aa_start": 767,
"aa_end": null,
"aa_length": 1024,
"cds_start": 2300,
"cds_end": null,
"cds_length": 3075,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000539363.2"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2636A>T",
"hgvs_p": "p.Lys879Met",
"transcript": "ENST00000889441.1",
"protein_id": "ENSP00000559500.1",
"transcript_support_level": null,
"aa_start": 879,
"aa_end": null,
"aa_length": 1136,
"cds_start": 2636,
"cds_end": null,
"cds_length": 3411,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000889441.1"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2729A>T",
"hgvs_p": "p.Lys910Met",
"transcript": "ENST00000889439.1",
"protein_id": "ENSP00000559498.1",
"transcript_support_level": null,
"aa_start": 910,
"aa_end": null,
"aa_length": 1129,
"cds_start": 2729,
"cds_end": null,
"cds_length": 3390,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000889439.1"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2729A>T",
"hgvs_p": "p.Lys910Met",
"transcript": "ENST00000965598.1",
"protein_id": "ENSP00000635657.1",
"transcript_support_level": null,
"aa_start": 910,
"aa_end": null,
"aa_length": 1129,
"cds_start": 2729,
"cds_end": null,
"cds_length": 3390,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000965598.1"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2486A>T",
"hgvs_p": "p.Lys829Met",
"transcript": "ENST00000889440.1",
"protein_id": "ENSP00000559499.1",
"transcript_support_level": null,
"aa_start": 829,
"aa_end": null,
"aa_length": 1086,
"cds_start": 2486,
"cds_end": null,
"cds_length": 3261,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000889440.1"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2336A>T",
"hgvs_p": "p.Lys779Met",
"transcript": "NM_001303040.2",
"protein_id": "NP_001289969.1",
"transcript_support_level": null,
"aa_start": 779,
"aa_end": null,
"aa_length": 1036,
"cds_start": 2336,
"cds_end": null,
"cds_length": 3111,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001303040.2"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2300A>T",
"hgvs_p": "p.Lys767Met",
"transcript": "NM_001303041.2",
"protein_id": "NP_001289970.1",
"transcript_support_level": null,
"aa_start": 767,
"aa_end": null,
"aa_length": 1024,
"cds_start": 2300,
"cds_end": null,
"cds_length": 3075,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001303041.2"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2771A>T",
"hgvs_p": "p.Lys924Met",
"transcript": "XM_017002622.1",
"protein_id": "XP_016858111.1",
"transcript_support_level": null,
"aa_start": 924,
"aa_end": null,
"aa_length": 1181,
"cds_start": 2771,
"cds_end": null,
"cds_length": 3546,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017002622.1"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2768A>T",
"hgvs_p": "p.Lys923Met",
"transcript": "XM_017002623.1",
"protein_id": "XP_016858112.1",
"transcript_support_level": null,
"aa_start": 923,
"aa_end": null,
"aa_length": 1180,
"cds_start": 2768,
"cds_end": null,
"cds_length": 3543,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017002623.1"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2726A>T",
"hgvs_p": "p.Lys909Met",
"transcript": "XM_047432895.1",
"protein_id": "XP_047288851.1",
"transcript_support_level": null,
"aa_start": 909,
"aa_end": null,
"aa_length": 1166,
"cds_start": 2726,
"cds_end": null,
"cds_length": 3501,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047432895.1"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2771A>T",
"hgvs_p": "p.Lys924Met",
"transcript": "XM_017002624.1",
"protein_id": "XP_016858113.1",
"transcript_support_level": null,
"aa_start": 924,
"aa_end": null,
"aa_length": 1143,
"cds_start": 2771,
"cds_end": null,
"cds_length": 3432,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017002624.1"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2771A>T",
"hgvs_p": "p.Lys924Met",
"transcript": "XM_017002625.1",
"protein_id": "XP_016858114.1",
"transcript_support_level": null,
"aa_start": 924,
"aa_end": null,
"aa_length": 1143,
"cds_start": 2771,
"cds_end": null,
"cds_length": 3432,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017002625.1"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2729A>T",
"hgvs_p": "p.Lys910Met",
"transcript": "XM_047432904.1",
"protein_id": "XP_047288860.1",
"transcript_support_level": null,
"aa_start": 910,
"aa_end": null,
"aa_length": 1129,
"cds_start": 2729,
"cds_end": null,
"cds_length": 3390,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047432904.1"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2729A>T",
"hgvs_p": "p.Lys910Met",
"transcript": "XM_047432906.1",
"protein_id": "XP_047288862.1",
"transcript_support_level": null,
"aa_start": 910,
"aa_end": null,
"aa_length": 1129,
"cds_start": 2729,
"cds_end": null,
"cds_length": 3390,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047432906.1"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2726A>T",
"hgvs_p": "p.Lys909Met",
"transcript": "XM_047432909.1",
"protein_id": "XP_047288865.1",
"transcript_support_level": null,
"aa_start": 909,
"aa_end": null,
"aa_length": 1128,
"cds_start": 2726,
"cds_end": null,
"cds_length": 3387,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047432909.1"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2771A>T",
"hgvs_p": "p.Lys924Met",
"transcript": "XM_047432910.1",
"protein_id": "XP_047288866.1",
"transcript_support_level": null,
"aa_start": 924,
"aa_end": null,
"aa_length": 1105,
"cds_start": 2771,
"cds_end": null,
"cds_length": 3318,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047432910.1"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2543A>T",
"hgvs_p": "p.Lys848Met",
"transcript": "XM_047432915.1",
"protein_id": "XP_047288871.1",
"transcript_support_level": null,
"aa_start": 848,
"aa_end": null,
"aa_length": 1105,
"cds_start": 2543,
"cds_end": null,
"cds_length": 3318,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047432915.1"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2528A>T",
"hgvs_p": "p.Lys843Met",
"transcript": "XM_017002626.1",
"protein_id": "XP_016858115.1",
"transcript_support_level": null,
"aa_start": 843,
"aa_end": null,
"aa_length": 1100,
"cds_start": 2528,
"cds_end": null,
"cds_length": 3303,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017002626.1"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2729A>T",
"hgvs_p": "p.Lys910Met",
"transcript": "XM_047432924.1",
"protein_id": "XP_047288880.1",
"transcript_support_level": null,
"aa_start": 910,
"aa_end": null,
"aa_length": 1091,
"cds_start": 2729,
"cds_end": null,
"cds_length": 3276,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047432924.1"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.2234A>T",
"hgvs_p": "p.Lys745Met",
"transcript": "XM_011510083.2",
"protein_id": "XP_011508385.1",
"transcript_support_level": null,
"aa_start": 745,
"aa_end": null,
"aa_length": 1002,
"cds_start": 2234,
"cds_end": null,
"cds_length": 3009,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011510083.2"
},
{
"aa_ref": "K",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "c.1202A>T",
"hgvs_p": "p.Lys401Met",
"transcript": "XM_011510084.1",
"protein_id": "XP_011508386.1",
"transcript_support_level": null,
"aa_start": 401,
"aa_end": null,
"aa_length": 658,
"cds_start": 1202,
"cds_end": null,
"cds_length": 1977,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011510084.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"hgvs_c": "n.2861A>T",
"hgvs_p": null,
"transcript": "XR_007064482.1",
"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": "XR_007064482.1"
}
],
"gene_symbol": "ITGA10",
"gene_hgnc_id": 6135,
"dbsnp": "rs781892285",
"frequency_reference_population": 0.0000055764294,
"hom_count_reference_population": 0,
"allele_count_reference_population": 9,
"gnomad_exomes_af": 0.00000478863,
"gnomad_genomes_af": 0.0000131458,
"gnomad_exomes_ac": 7,
"gnomad_genomes_ac": 2,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.2558932304382324,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.07000000029802322,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": null,
"revel_prediction": null,
"alphamissense_score": 0.1545,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.18,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 0.534,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.07,
"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": 0,
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4_Moderate",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 2,
"pathogenic_score": 2,
"criteria": [
"PM2",
"BP4_Moderate"
],
"verdict": "Uncertain_significance",
"transcript": "NM_003637.5",
"gene_symbol": "ITGA10",
"hgnc_id": 6135,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.2729A>T",
"hgvs_p": "p.Lys910Met"
}
],
"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
}