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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: 5-176943430-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=176943430&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "5",
"pos": 176943430,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_016290.4",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.1502A>G",
"hgvs_p": "p.Asn501Ser",
"transcript": "NM_001199298.2",
"protein_id": "NP_001186227.1",
"transcript_support_level": null,
"aa_start": 501,
"aa_end": null,
"aa_length": 719,
"cds_start": 1502,
"cds_end": null,
"cds_length": 2160,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000511320.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001199298.2"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.1502A>G",
"hgvs_p": "p.Asn501Ser",
"transcript": "ENST00000511320.6",
"protein_id": "ENSP00000421926.1",
"transcript_support_level": 1,
"aa_start": 501,
"aa_end": null,
"aa_length": 719,
"cds_start": 1502,
"cds_end": null,
"cds_length": 2160,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001199298.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000511320.6"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.1502A>G",
"hgvs_p": "p.Asn501Ser",
"transcript": "ENST00000377227.8",
"protein_id": "ENSP00000366434.4",
"transcript_support_level": 1,
"aa_start": 501,
"aa_end": null,
"aa_length": 719,
"cds_start": 1502,
"cds_end": null,
"cds_length": 2160,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000377227.8"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.1004A>G",
"hgvs_p": "p.Asn335Ser",
"transcript": "ENST00000506128.5",
"protein_id": "ENSP00000427480.1",
"transcript_support_level": 1,
"aa_start": 335,
"aa_end": null,
"aa_length": 553,
"cds_start": 1004,
"cds_end": null,
"cds_length": 1662,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000506128.5"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.392A>G",
"hgvs_p": "p.Asn131Ser",
"transcript": "ENST00000510698.2",
"protein_id": "ENSP00000423717.2",
"transcript_support_level": 1,
"aa_start": 131,
"aa_end": null,
"aa_length": 349,
"cds_start": 392,
"cds_end": null,
"cds_length": 1050,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000510698.2"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.1502A>G",
"hgvs_p": "p.Asn501Ser",
"transcript": "NM_001199297.2",
"protein_id": "NP_001186226.1",
"transcript_support_level": null,
"aa_start": 501,
"aa_end": null,
"aa_length": 719,
"cds_start": 1502,
"cds_end": null,
"cds_length": 2160,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001199297.2"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.1502A>G",
"hgvs_p": "p.Asn501Ser",
"transcript": "NM_016290.4",
"protein_id": "NP_057374.3",
"transcript_support_level": null,
"aa_start": 501,
"aa_end": null,
"aa_length": 719,
"cds_start": 1502,
"cds_end": null,
"cds_length": 2160,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_016290.4"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.1502A>G",
"hgvs_p": "p.Asn501Ser",
"transcript": "ENST00000890107.1",
"protein_id": "ENSP00000560166.1",
"transcript_support_level": null,
"aa_start": 501,
"aa_end": null,
"aa_length": 719,
"cds_start": 1502,
"cds_end": null,
"cds_length": 2160,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000890107.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.1502A>G",
"hgvs_p": "p.Asn501Ser",
"transcript": "ENST00000924857.1",
"protein_id": "ENSP00000594916.1",
"transcript_support_level": null,
"aa_start": 501,
"aa_end": null,
"aa_length": 719,
"cds_start": 1502,
"cds_end": null,
"cds_length": 2160,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000924857.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.1004A>G",
"hgvs_p": "p.Asn335Ser",
"transcript": "NM_001317961.1",
"protein_id": "NP_001304890.1",
"transcript_support_level": null,
"aa_start": 335,
"aa_end": null,
"aa_length": 553,
"cds_start": 1004,
"cds_end": null,
"cds_length": 1662,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001317961.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.659A>G",
"hgvs_p": "p.Asn220Ser",
"transcript": "ENST00000970269.1",
"protein_id": "ENSP00000640328.1",
"transcript_support_level": null,
"aa_start": 220,
"aa_end": null,
"aa_length": 479,
"cds_start": 659,
"cds_end": null,
"cds_length": 1440,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000970269.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.659A>G",
"hgvs_p": "p.Asn220Ser",
"transcript": "ENST00000890105.1",
"protein_id": "ENSP00000560164.1",
"transcript_support_level": null,
"aa_start": 220,
"aa_end": null,
"aa_length": 438,
"cds_start": 659,
"cds_end": null,
"cds_length": 1317,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000890105.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.659A>G",
"hgvs_p": "p.Asn220Ser",
"transcript": "ENST00000890106.1",
"protein_id": "ENSP00000560165.1",
"transcript_support_level": null,
"aa_start": 220,
"aa_end": null,
"aa_length": 438,
"cds_start": 659,
"cds_end": null,
"cds_length": 1317,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000890106.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.659A>G",
"hgvs_p": "p.Asn220Ser",
"transcript": "ENST00000890108.1",
"protein_id": "ENSP00000560167.1",
"transcript_support_level": null,
"aa_start": 220,
"aa_end": null,
"aa_length": 438,
"cds_start": 659,
"cds_end": null,
"cds_length": 1317,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000890108.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.659A>G",
"hgvs_p": "p.Asn220Ser",
"transcript": "ENST00000890110.1",
"protein_id": "ENSP00000560169.1",
"transcript_support_level": null,
"aa_start": 220,
"aa_end": null,
"aa_length": 438,
"cds_start": 659,
"cds_end": null,
"cds_length": 1317,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000890110.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.1502A>G",
"hgvs_p": "p.Asn501Ser",
"transcript": "XM_005265930.3",
"protein_id": "XP_005265987.1",
"transcript_support_level": null,
"aa_start": 501,
"aa_end": null,
"aa_length": 719,
"cds_start": 1502,
"cds_end": null,
"cds_length": 2160,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005265930.3"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.1502A>G",
"hgvs_p": "p.Asn501Ser",
"transcript": "XM_006714871.3",
"protein_id": "XP_006714934.1",
"transcript_support_level": null,
"aa_start": 501,
"aa_end": null,
"aa_length": 719,
"cds_start": 1502,
"cds_end": null,
"cds_length": 2160,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006714871.3"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.1205A>G",
"hgvs_p": "p.Asn402Ser",
"transcript": "XM_047417303.1",
"protein_id": "XP_047273259.1",
"transcript_support_level": null,
"aa_start": 402,
"aa_end": null,
"aa_length": 620,
"cds_start": 1205,
"cds_end": null,
"cds_length": 1863,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047417303.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.1502A>G",
"hgvs_p": "p.Asn501Ser",
"transcript": "XM_011534570.2",
"protein_id": "XP_011532872.1",
"transcript_support_level": null,
"aa_start": 501,
"aa_end": null,
"aa_length": 537,
"cds_start": 1502,
"cds_end": null,
"cds_length": 1614,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011534570.2"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.659A>G",
"hgvs_p": "p.Asn220Ser",
"transcript": "XM_005265932.4",
"protein_id": "XP_005265989.1",
"transcript_support_level": null,
"aa_start": 220,
"aa_end": null,
"aa_length": 438,
"cds_start": 659,
"cds_end": null,
"cds_length": 1317,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005265932.4"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.659A>G",
"hgvs_p": "p.Asn220Ser",
"transcript": "XM_005265933.3",
"protein_id": "XP_005265990.1",
"transcript_support_level": null,
"aa_start": 220,
"aa_end": null,
"aa_length": 438,
"cds_start": 659,
"cds_end": null,
"cds_length": 1317,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005265933.3"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "UIMC1",
"gene_hgnc_id": 30298,
"hgvs_c": "c.659A>G",
"hgvs_p": "p.Asn220Ser",
"transcript": "XM_017009576.2",
"protein_id": "XP_016865065.1",
"transcript_support_level": null,
"aa_start": 220,
"aa_end": null,
"aa_length": 438,
"cds_start": 659,
"cds_end": null,
"cds_length": 1317,
"cdna_start": null,
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"cdna_length": null,
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{
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{
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{
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{
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{
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{
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],
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],
"gene_symbol": "UIMC1",
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"dbsnp": "rs529063071",
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"computational_score_selected": 0.008883088827133179,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.05000000074505806,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.003,
"revel_prediction": "Benign",
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"bayesdelnoaf_score": -0.81,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": -1.37,
"phylop100way_prediction": "Benign",
"spliceai_max_score": 0.05,
"spliceai_max_prediction": "Benign",
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"apogee2_prediction": null,
"mitotip_score": null,
"mitotip_prediction": null,
"acmg_score": -4,
"acmg_classification": "Likely_benign",
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"acmg_by_gene": [
{
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"pathogenic_score": 0,
"criteria": [
"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "NM_016290.4",
"gene_symbol": "UIMC1",
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"effects": [
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],
"inheritance_mode": "Unknown",
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],
"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
}