← Back to variant description
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: 14-104770411-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=104770411&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "14",
"pos": 104770411,
"ref": "A",
"alt": "G",
"effect": "missense_variant",
"transcript": "ENST00000649815.2",
"consequences": [
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "NM_001382430.1",
"protein_id": "NP_001369359.1",
"transcript_support_level": null,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 1895,
"cdna_end": null,
"cdna_length": 2957,
"mane_select": "ENST00000649815.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "ENST00000649815.2",
"protein_id": "ENSP00000497822.1",
"transcript_support_level": null,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 1895,
"cdna_end": null,
"cdna_length": 2957,
"mane_select": "NM_001382430.1",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "ENST00000349310.7",
"protein_id": "ENSP00000270202.4",
"transcript_support_level": 1,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 1804,
"cdna_end": null,
"cdna_length": 2866,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "ENST00000402615.6",
"protein_id": "ENSP00000385326.2",
"transcript_support_level": 1,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 2854,
"cdna_end": null,
"cdna_length": 3913,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "ENST00000407796.7",
"protein_id": "ENSP00000384293.2",
"transcript_support_level": 1,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 1717,
"cdna_end": null,
"cdna_length": 2779,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "ENST00000554581.5",
"protein_id": "ENSP00000451828.1",
"transcript_support_level": 1,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 2854,
"cdna_end": null,
"cdna_length": 3916,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "ENST00000554848.5",
"protein_id": "ENSP00000451166.1",
"transcript_support_level": 1,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 1525,
"cdna_end": null,
"cdna_length": 1595,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "ENST00000555528.5",
"protein_id": "ENSP00000450688.1",
"transcript_support_level": 1,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 2026,
"cdna_end": null,
"cdna_length": 3066,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1520T>C",
"hgvs_p": "p.Met507Thr",
"transcript": "ENST00000714130.1",
"protein_id": "ENSP00000519419.1",
"transcript_support_level": null,
"aa_start": 507,
"aa_end": null,
"aa_length": 529,
"cds_start": 1520,
"cds_end": null,
"cds_length": 1590,
"cdna_start": 2098,
"cdna_end": null,
"cdna_length": 3155,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1448T>C",
"hgvs_p": "p.Met483Thr",
"transcript": "ENST00000553797.2",
"protein_id": "ENSP00000507566.1",
"transcript_support_level": 3,
"aa_start": 483,
"aa_end": null,
"aa_length": 505,
"cds_start": 1448,
"cds_end": null,
"cds_length": 1518,
"cdna_start": 2696,
"cdna_end": null,
"cdna_length": 3711,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "NM_001014431.2",
"protein_id": "NP_001014431.1",
"transcript_support_level": null,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 1717,
"cdna_end": null,
"cdna_length": 2779,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "NM_001014432.2",
"protein_id": "NP_001014432.1",
"transcript_support_level": null,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 1801,
"cdna_end": null,
"cdna_length": 2863,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "NM_001382431.1",
"protein_id": "NP_001369360.1",
"transcript_support_level": null,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 1860,
"cdna_end": null,
"cdna_length": 2922,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "NM_001382432.1",
"protein_id": "NP_001369361.1",
"transcript_support_level": null,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 1944,
"cdna_end": null,
"cdna_length": 3006,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "NM_001382433.1",
"protein_id": "NP_001369362.1",
"transcript_support_level": null,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 2013,
"cdna_end": null,
"cdna_length": 3075,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "NM_005163.2",
"protein_id": "NP_005154.2",
"transcript_support_level": null,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 1927,
"cdna_end": null,
"cdna_length": 2989,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "ENST00000683722.1",
"protein_id": "ENSP00000507879.1",
"transcript_support_level": null,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 1569,
"cdna_end": null,
"cdna_length": 2609,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1274T>C",
"hgvs_p": "p.Met425Thr",
"transcript": "ENST00000554192.6",
"protein_id": "ENSP00000450681.3",
"transcript_support_level": 2,
"aa_start": 425,
"aa_end": null,
"aa_length": 447,
"cds_start": 1274,
"cds_end": null,
"cds_length": 1344,
"cdna_start": 1618,
"cdna_end": null,
"cdna_length": 2057,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1247T>C",
"hgvs_p": "p.Met416Thr",
"transcript": "ENST00000714123.1",
"protein_id": "ENSP00000519414.1",
"transcript_support_level": null,
"aa_start": 416,
"aa_end": null,
"aa_length": 438,
"cds_start": 1247,
"cds_end": null,
"cds_length": 1317,
"cdna_start": 1602,
"cdna_end": null,
"cdna_length": 2664,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "XM_047431069.1",
"protein_id": "XP_047287025.1",
"transcript_support_level": null,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 2719,
"cdna_end": null,
"cdna_length": 3781,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "XM_047431070.1",
"protein_id": "XP_047287026.1",
"transcript_support_level": null,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 2507,
"cdna_end": null,
"cdna_length": 3569,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "XM_047431071.1",
"protein_id": "XP_047287027.1",
"transcript_support_level": null,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 2424,
"cdna_end": null,
"cdna_length": 3486,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "XM_047431072.1",
"protein_id": "XP_047287028.1",
"transcript_support_level": null,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 2204,
"cdna_end": null,
"cdna_length": 3266,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "XM_047431073.1",
"protein_id": "XP_047287029.1",
"transcript_support_level": null,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 2616,
"cdna_end": null,
"cdna_length": 3678,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "XM_047431074.1",
"protein_id": "XP_047287030.1",
"transcript_support_level": null,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 2852,
"cdna_end": null,
"cdna_length": 3914,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "M",
"aa_alt": "T",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr",
"transcript": "XM_047431075.1",
"protein_id": "XP_047287031.1",
"transcript_support_level": null,
"aa_start": 458,
"aa_end": null,
"aa_length": 480,
"cds_start": 1373,
"cds_end": null,
"cds_length": 1443,
"cdna_start": 2038,
"cdna_end": null,
"cdna_length": 3100,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "n.1308T>C",
"hgvs_p": null,
"transcript": "ENST00000544168.5",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1564,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "n.1771T>C",
"hgvs_p": null,
"transcript": "ENST00000553506.5",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2830,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "n.*199T>C",
"hgvs_p": null,
"transcript": "ENST00000554585.6",
"protein_id": "ENSP00000481526.2",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2030,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "n.1842T>C",
"hgvs_p": null,
"transcript": "ENST00000554826.2",
"protein_id": null,
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2857,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "n.7337T>C",
"hgvs_p": null,
"transcript": "ENST00000557552.1",
"protein_id": null,
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8396,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "n.3359T>C",
"hgvs_p": null,
"transcript": "ENST00000610370.2",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4373,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "n.1250T>C",
"hgvs_p": null,
"transcript": "ENST00000683058.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2277,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "n.930T>C",
"hgvs_p": null,
"transcript": "ENST00000684058.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1945,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "n.*199T>C",
"hgvs_p": null,
"transcript": "ENST00000554585.6",
"protein_id": "ENSP00000481526.2",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2030,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 14,
"intron_rank": 13,
"intron_rank_end": null,
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"hgvs_c": "c.1363+334T>C",
"hgvs_p": null,
"transcript": "ENST00000555458.6",
"protein_id": "ENSP00000451470.3",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 467,
"cds_start": -4,
"cds_end": null,
"cds_length": 1404,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1942,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ENSG00000258430",
"gene_hgnc_id": null,
"hgvs_c": "n.*140A>G",
"hgvs_p": null,
"transcript": "ENST00000557223.1",
"protein_id": null,
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 663,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
}
],
"gene_symbol": "AKT1",
"gene_hgnc_id": 391,
"dbsnp": "rs587778018",
"frequency_reference_population": 0.000032892614,
"hom_count_reference_population": 0,
"allele_count_reference_population": 53,
"gnomad_exomes_af": 0.0000308407,
"gnomad_genomes_af": 0.0000525645,
"gnomad_exomes_ac": 45,
"gnomad_genomes_ac": 8,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.14931204915046692,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.137,
"revel_prediction": "Benign",
"alphamissense_score": 0.0811,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.31,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 9.188,
"phylop100way_prediction": "Pathogenic",
"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": -7,
"acmg_classification": "Benign",
"acmg_criteria": "BP4_Moderate,BS1_Supporting,BS2",
"acmg_by_gene": [
{
"score": -7,
"benign_score": 7,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate",
"BS1_Supporting",
"BS2"
],
"verdict": "Benign",
"transcript": "ENST00000649815.2",
"gene_symbol": "AKT1",
"hgnc_id": 391,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD,Unknown",
"hgvs_c": "c.1373T>C",
"hgvs_p": "p.Met458Thr"
},
{
"score": -2,
"benign_score": 2,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate"
],
"verdict": "Likely_benign",
"transcript": "ENST00000557223.1",
"gene_symbol": "ENSG00000258430",
"hgnc_id": null,
"effects": [
"downstream_gene_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.*140A>G",
"hgvs_p": null
}
],
"clinvar_disease": "Cowden syndrome 6,not specified",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1 O:1",
"phenotype_combined": "not specified|Cowden syndrome 6",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}