← 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: 18-76379020-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=18&pos=76379020&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "18",
"pos": 76379020,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_014643.4",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "NM_014643.4",
"protein_id": "NP_055458.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000443185.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_014643.4"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "ENST00000443185.7",
"protein_id": "ENSP00000394757.2",
"transcript_support_level": 1,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_014643.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000443185.7"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.1264G>A",
"hgvs_p": "p.Val422Met",
"transcript": "ENST00000617840.1",
"protein_id": "ENSP00000478712.1",
"transcript_support_level": 1,
"aa_start": 422,
"aa_end": null,
"aa_length": 516,
"cds_start": 1264,
"cds_end": null,
"cds_length": 1551,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000617840.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "ENST00000871208.1",
"protein_id": "ENSP00000541267.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000871208.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "ENST00000871209.1",
"protein_id": "ENSP00000541268.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000871209.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "ENST00000871210.1",
"protein_id": "ENSP00000541269.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000871210.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "ENST00000915360.1",
"protein_id": "ENSP00000585419.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000915360.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "ENST00000915361.1",
"protein_id": "ENSP00000585420.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000915361.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "ENST00000915362.1",
"protein_id": "ENSP00000585421.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000915362.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "ENST00000957637.1",
"protein_id": "ENSP00000627696.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000957637.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "ENST00000957638.1",
"protein_id": "ENSP00000627697.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000957638.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "ENST00000957639.1",
"protein_id": "ENSP00000627698.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000957639.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "XM_011526269.3",
"protein_id": "XP_011524571.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011526269.3"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "XM_011526270.4",
"protein_id": "XP_011524572.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011526270.4"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "XM_011526273.4",
"protein_id": "XP_011524575.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011526273.4"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "XM_011526274.4",
"protein_id": "XP_011524576.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011526274.4"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "XM_011526275.3",
"protein_id": "XP_011524577.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011526275.3"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "XM_017026097.3",
"protein_id": "XP_016881586.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017026097.3"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "XM_047437950.1",
"protein_id": "XP_047293906.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047437950.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "XM_047437951.1",
"protein_id": "XP_047293907.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047437951.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "XM_047437952.1",
"protein_id": "XP_047293908.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047437952.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "XM_047437953.1",
"protein_id": "XP_047293909.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047437953.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "XM_047437954.1",
"protein_id": "XP_047293910.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047437954.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "XM_047437955.1",
"protein_id": "XP_047293911.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047437955.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "XM_047437956.1",
"protein_id": "XP_047293912.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1163,
"cds_start": 3094,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047437956.1"
},
{
"aa_ref": "V",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met",
"transcript": "XM_047437957.1",
"protein_id": "XP_047293913.1",
"transcript_support_level": null,
"aa_start": 1032,
"aa_end": null,
"aa_length": 1091,
"cds_start": 3094,
"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_047437957.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "n.33765G>A",
"hgvs_p": null,
"transcript": "XR_007066258.1",
"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_007066258.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"upstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"hgvs_c": "c.-108G>A",
"hgvs_p": null,
"transcript": "ENST00000542818.1",
"protein_id": "ENSP00000445902.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 24,
"cds_start": null,
"cds_end": null,
"cds_length": 75,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000542818.1"
}
],
"gene_symbol": "ZNF516",
"gene_hgnc_id": 28990,
"dbsnp": "rs200905294",
"frequency_reference_population": 0.000011206198,
"hom_count_reference_population": 0,
"allele_count_reference_population": 18,
"gnomad_exomes_af": 0.0000109797,
"gnomad_genomes_af": 0.0000134216,
"gnomad_exomes_ac": 16,
"gnomad_genomes_ac": 2,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.08058673143386841,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.009,
"revel_prediction": "Benign",
"alphamissense_score": 0.0846,
"alphamissense_prediction": "Benign",
"bayesdelnoaf_score": -0.81,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -0.267,
"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": 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_014643.4",
"gene_symbol": "ZNF516",
"hgnc_id": 28990,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.3094G>A",
"hgvs_p": "p.Val1032Met"
}
],
"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
}