← 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: 20-49863011-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=20&pos=49863011&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"message": null,
"variants": [
{
"acmg_by_gene": [
{
"benign_score": 1,
"criteria": [
"PM2",
"BP4"
],
"effects": [
"missense_variant"
],
"gene_symbol": "SLC9A8",
"hgnc_id": 20728,
"hgvs_c": "c.844A>G",
"hgvs_p": "p.Lys282Glu",
"inheritance_mode": "AR",
"pathogenic_score": 2,
"score": 1,
"transcript": "NM_001260491.2",
"verdict": "Uncertain_significance"
}
],
"acmg_classification": "Uncertain_significance",
"acmg_criteria": "PM2,BP4",
"acmg_score": 1,
"allele_count_reference_population": 15,
"alphamissense_prediction": null,
"alphamissense_score": 0.2788,
"alt": "G",
"apogee2_prediction": null,
"apogee2_score": null,
"bayesdelnoaf_prediction": "Uncertain_significance",
"bayesdelnoaf_score": -0.02,
"chr": "20",
"clinvar_classification": "Uncertain significance",
"clinvar_disease": "not specified",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"computational_prediction_selected": "Benign",
"computational_score_selected": 0.31633126735687256,
"computational_source_selected": "MetaRNN",
"consequences": [
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 581,
"aa_ref": "K",
"aa_start": 266,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6147,
"cdna_start": 891,
"cds_end": null,
"cds_length": 1746,
"cds_start": 796,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "NM_015266.3",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.796A>G",
"hgvs_p": "p.Lys266Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "ENST00000361573.3",
"protein_coding": true,
"protein_id": "NP_056081.1",
"strand": true,
"transcript": "NM_015266.3",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 581,
"aa_ref": "K",
"aa_start": 266,
"biotype": "protein_coding",
"canonical": true,
"cdna_end": null,
"cdna_length": 6147,
"cdna_start": 891,
"cds_end": null,
"cds_length": 1746,
"cds_start": 796,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000361573.3",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.796A>G",
"hgvs_p": "p.Lys266Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": "NM_015266.3",
"protein_coding": true,
"protein_id": "ENSP00000354966.2",
"strand": true,
"transcript": "ENST00000361573.3",
"transcript_support_level": 1
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 614,
"aa_ref": "K",
"aa_start": 299,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3601,
"cdna_start": 956,
"cds_end": null,
"cds_length": 1845,
"cds_start": 895,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "ENST00000851371.1",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.895A>G",
"hgvs_p": "p.Lys299Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000521430.1",
"strand": true,
"transcript": "ENST00000851371.1",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 597,
"aa_ref": "K",
"aa_start": 282,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6195,
"cdna_start": 939,
"cds_end": null,
"cds_length": 1794,
"cds_start": 844,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "NM_001260491.2",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.844A>G",
"hgvs_p": "p.Lys282Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "NP_001247420.1",
"strand": true,
"transcript": "NM_001260491.2",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 597,
"aa_ref": "K",
"aa_start": 282,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6309,
"cdna_start": 1054,
"cds_end": null,
"cds_length": 1794,
"cds_start": 844,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000417961.5",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.844A>G",
"hgvs_p": "p.Lys282Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000416418.1",
"strand": true,
"transcript": "ENST00000417961.5",
"transcript_support_level": 2
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 593,
"aa_ref": "K",
"aa_start": 266,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4336,
"cdna_start": 891,
"cds_end": null,
"cds_length": 1782,
"cds_start": 796,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000851370.1",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.796A>G",
"hgvs_p": "p.Lys266Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000521429.1",
"strand": true,
"transcript": "ENST00000851370.1",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 580,
"aa_ref": "K",
"aa_start": 265,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 3462,
"cdna_start": 813,
"cds_end": null,
"cds_length": 1743,
"cds_start": 793,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000851372.1",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.793A>G",
"hgvs_p": "p.Lys265Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000521431.1",
"strand": true,
"transcript": "ENST00000851372.1",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 553,
"aa_ref": "K",
"aa_start": 238,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 4596,
"cdna_start": 795,
"cds_end": null,
"cds_length": 1662,
"cds_start": 712,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "ENST00000851369.1",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.712A>G",
"hgvs_p": "p.Lys238Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000521428.1",
"strand": true,
"transcript": "ENST00000851369.1",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 552,
"aa_ref": "K",
"aa_start": 266,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5978,
"cdna_start": 816,
"cds_end": null,
"cds_length": 1659,
"cds_start": 796,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "ENST00000851368.1",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.796A>G",
"hgvs_p": "p.Lys266Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "ENSP00000521427.1",
"strand": true,
"transcript": "ENST00000851368.1",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 630,
"aa_ref": "K",
"aa_start": 315,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6294,
"cdna_start": 1038,
"cds_end": null,
"cds_length": 1893,
"cds_start": 943,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "XM_011528736.3",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.943A>G",
"hgvs_p": "p.Lys315Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011527038.1",
"strand": true,
"transcript": "XM_011528736.3",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 614,
"aa_ref": "K",
"aa_start": 299,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6246,
"cdna_start": 990,
"cds_end": null,
"cds_length": 1845,
"cds_start": 895,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "XM_006723756.2",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.895A>G",
"hgvs_p": "p.Lys299Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_006723819.1",
"strand": true,
"transcript": "XM_006723756.2",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 602,
"aa_ref": "K",
"aa_start": 287,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6210,
"cdna_start": 954,
"cds_end": null,
"cds_length": 1809,
"cds_start": 859,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "XM_011528737.2",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.859A>G",
"hgvs_p": "p.Lys287Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011527039.1",
"strand": true,
"transcript": "XM_011528737.2",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 591,
"aa_ref": "K",
"aa_start": 315,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6177,
"cdna_start": 1038,
"cds_end": null,
"cds_length": 1776,
"cds_start": 943,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "XM_011528738.3",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.943A>G",
"hgvs_p": "p.Lys315Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011527040.1",
"strand": true,
"transcript": "XM_011528738.3",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 571,
"aa_ref": "K",
"aa_start": 256,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6291,
"cdna_start": 1035,
"cds_end": null,
"cds_length": 1716,
"cds_start": 766,
"consequences": [
"missense_variant"
],
"exon_count": 17,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "XM_047440069.1",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.766A>G",
"hgvs_p": "p.Lys256Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047296025.1",
"strand": true,
"transcript": "XM_047440069.1",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 565,
"aa_ref": "K",
"aa_start": 315,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 2735,
"cdna_start": 1038,
"cds_end": null,
"cds_length": 1698,
"cds_start": 943,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "XM_017027754.3",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.943A>G",
"hgvs_p": "p.Lys315Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_016883243.1",
"strand": true,
"transcript": "XM_017027754.3",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 564,
"aa_ref": "K",
"aa_start": 315,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1885,
"cdna_start": 1038,
"cds_end": null,
"cds_length": 1695,
"cds_start": 943,
"consequences": [
"missense_variant"
],
"exon_count": 16,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "XM_011528740.3",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.943A>G",
"hgvs_p": "p.Lys315Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011527042.1",
"strand": true,
"transcript": "XM_011528740.3",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 558,
"aa_ref": "K",
"aa_start": 282,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6078,
"cdna_start": 939,
"cds_end": null,
"cds_length": 1677,
"cds_start": 844,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "XM_011528741.3",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.844A>G",
"hgvs_p": "p.Lys282Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011527043.1",
"strand": true,
"transcript": "XM_011528741.3",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 553,
"aa_ref": "K",
"aa_start": 238,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6063,
"cdna_start": 807,
"cds_end": null,
"cds_length": 1662,
"cds_start": 712,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "XM_047440070.1",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.712A>G",
"hgvs_p": "p.Lys238Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047296026.1",
"strand": true,
"transcript": "XM_047440070.1",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 542,
"aa_ref": "K",
"aa_start": 266,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 6030,
"cdna_start": 891,
"cds_end": null,
"cds_length": 1629,
"cds_start": 796,
"consequences": [
"missense_variant"
],
"exon_count": 15,
"exon_rank": 9,
"exon_rank_end": null,
"feature": "XM_047440071.1",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.796A>G",
"hgvs_p": "p.Lys266Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047296027.1",
"strand": true,
"transcript": "XM_047440071.1",
"transcript_support_level": null
},
{
"aa_alt": "E",
"aa_end": null,
"aa_length": 395,
"aa_ref": "K",
"aa_start": 80,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 5678,
"cdna_start": 422,
"cds_end": null,
"cds_length": 1188,
"cds_start": 238,
"consequences": [
"missense_variant"
],
"exon_count": 11,
"exon_rank": 4,
"exon_rank_end": null,
"feature": "XM_047440072.1",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.238A>G",
"hgvs_p": "p.Lys80Glu",
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047296028.1",
"strand": true,
"transcript": "XM_047440072.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 299,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1104,
"cdna_start": null,
"cds_end": null,
"cds_length": 900,
"cds_start": null,
"consequences": [
"3_prime_UTR_variant"
],
"exon_count": 11,
"exon_rank": 11,
"exon_rank_end": null,
"feature": "XM_011528745.3",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.*99A>G",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_011527047.1",
"strand": true,
"transcript": "XM_011528745.3",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": 293,
"aa_ref": null,
"aa_start": null,
"biotype": "protein_coding",
"canonical": false,
"cdna_end": null,
"cdna_length": 1075,
"cdna_start": null,
"cds_end": null,
"cds_length": 882,
"cds_start": null,
"consequences": [
"3_prime_UTR_variant"
],
"exon_count": 10,
"exon_rank": 10,
"exon_rank_end": null,
"feature": "XM_047440073.1",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "c.*66A>G",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": true,
"protein_id": "XP_047296029.1",
"strand": true,
"transcript": "XM_047440073.1",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 6112,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 15,
"exon_rank": 8,
"exon_rank_end": null,
"feature": "NR_048537.2",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "n.856A>G",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": true,
"transcript": "NR_048537.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 6028,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 14,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "NR_048538.2",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "n.772A>G",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": true,
"transcript": "NR_048538.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 5810,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_count": 12,
"exon_rank": 7,
"exon_rank_end": null,
"feature": "NR_048540.2",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "n.754A>G",
"hgvs_p": null,
"intron_rank": null,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": true,
"transcript": "NR_048540.2",
"transcript_support_level": null
},
{
"aa_alt": null,
"aa_end": null,
"aa_length": null,
"aa_ref": null,
"aa_start": null,
"biotype": "pseudogene",
"canonical": false,
"cdna_end": null,
"cdna_length": 5984,
"cdna_start": null,
"cds_end": null,
"cds_length": null,
"cds_start": null,
"consequences": [
"intron_variant"
],
"exon_count": 14,
"exon_rank": null,
"exon_rank_end": null,
"feature": "NR_048539.2",
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"hgvs_c": "n.774-1717A>G",
"hgvs_p": null,
"intron_rank": 7,
"intron_rank_end": null,
"mane_plus": null,
"mane_select": null,
"protein_coding": false,
"protein_id": null,
"strand": true,
"transcript": "NR_048539.2",
"transcript_support_level": null
}
],
"custom_annotations": null,
"dbscsnv_ada_prediction": null,
"dbscsnv_ada_score": null,
"dbsnp": "rs376467705",
"effect": "missense_variant",
"frequency_reference_population": 0.000009293922,
"gene_hgnc_id": 20728,
"gene_symbol": "SLC9A8",
"gnomad_exomes_ac": 14,
"gnomad_exomes_af": 0.00000957769,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_ac": 1,
"gnomad_genomes_af": 0.00000656909,
"gnomad_genomes_homalt": 0,
"gnomad_mito_heteroplasmic": null,
"gnomad_mito_homoplasmic": null,
"hom_count_reference_population": 0,
"mitotip_prediction": null,
"mitotip_score": null,
"pathogenicity_classification_combined": "Uncertain significance",
"phenotype_combined": "not specified",
"phylop100way_prediction": "Uncertain_significance",
"phylop100way_score": 6.733,
"pos": 49863011,
"ref": "A",
"revel_prediction": "Benign",
"revel_score": 0.276,
"splice_prediction_selected": "Benign",
"splice_score_selected": 0,
"splice_source_selected": "max_spliceai",
"spliceai_max_prediction": "Benign",
"spliceai_max_score": 0,
"transcript": "NM_001260491.2"
}
]
}