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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: 2-1910340-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=1910340&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 1910340,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "ENST00000647738.2",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1717G>A",
"hgvs_p": "p.Gly573Arg",
"transcript": "NM_001303052.2",
"protein_id": "NP_001289981.1",
"transcript_support_level": null,
"aa_start": 573,
"aa_end": null,
"aa_length": 1186,
"cds_start": 1717,
"cds_end": null,
"cds_length": 3561,
"cdna_start": 2546,
"cdna_end": null,
"cdna_length": 7144,
"mane_select": "ENST00000647738.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1717G>A",
"hgvs_p": "p.Gly573Arg",
"transcript": "ENST00000647738.2",
"protein_id": "ENSP00000497479.2",
"transcript_support_level": null,
"aa_start": 573,
"aa_end": null,
"aa_length": 1186,
"cds_start": 1717,
"cds_end": null,
"cds_length": 3561,
"cdna_start": 2546,
"cdna_end": null,
"cdna_length": 7144,
"mane_select": "NM_001303052.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1717G>A",
"hgvs_p": "p.Gly573Arg",
"transcript": "ENST00000428368.7",
"protein_id": "ENSP00000396103.3",
"transcript_support_level": 1,
"aa_start": 573,
"aa_end": null,
"aa_length": 1186,
"cds_start": 1717,
"cds_end": null,
"cds_length": 3561,
"cdna_start": 2604,
"cdna_end": null,
"cdna_length": 6951,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1711G>A",
"hgvs_p": "p.Gly571Arg",
"transcript": "ENST00000399161.8",
"protein_id": "ENSP00000382114.3",
"transcript_support_level": 1,
"aa_start": 571,
"aa_end": null,
"aa_length": 1184,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3555,
"cdna_start": 2640,
"cdna_end": null,
"cdna_length": 7227,
"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": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "n.1210G>A",
"hgvs_p": null,
"transcript": "ENST00000602387.6",
"protein_id": "ENSP00000473409.2",
"transcript_support_level": 1,
"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": 2381,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1717G>A",
"hgvs_p": "p.Gly573Arg",
"transcript": "ENST00000644820.1",
"protein_id": "ENSP00000496210.1",
"transcript_support_level": null,
"aa_start": 573,
"aa_end": null,
"aa_length": 1207,
"cds_start": 1717,
"cds_end": null,
"cds_length": 3624,
"cdna_start": 2619,
"cdna_end": null,
"cdna_length": 7269,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1717G>A",
"hgvs_p": "p.Gly573Arg",
"transcript": "NM_001329844.2",
"protein_id": "NP_001316773.1",
"transcript_support_level": null,
"aa_start": 573,
"aa_end": null,
"aa_length": 1186,
"cds_start": 1717,
"cds_end": null,
"cds_length": 3561,
"cdna_start": 2622,
"cdna_end": null,
"cdna_length": 7220,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1717G>A",
"hgvs_p": "p.Gly573Arg",
"transcript": "NM_001329845.1",
"protein_id": "NP_001316774.1",
"transcript_support_level": null,
"aa_start": 573,
"aa_end": null,
"aa_length": 1186,
"cds_start": 1717,
"cds_end": null,
"cds_length": 3561,
"cdna_start": 2412,
"cdna_end": null,
"cdna_length": 7010,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1717G>A",
"hgvs_p": "p.Gly573Arg",
"transcript": "ENST00000647694.1",
"protein_id": "ENSP00000497722.1",
"transcript_support_level": null,
"aa_start": 573,
"aa_end": null,
"aa_length": 1186,
"cds_start": 1717,
"cds_end": null,
"cds_length": 3561,
"cdna_start": 2412,
"cdna_end": null,
"cdna_length": 6804,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1711G>A",
"hgvs_p": "p.Gly571Arg",
"transcript": "ENST00000650485.2",
"protein_id": "ENSP00000497068.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1186,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3561,
"cdna_start": 2612,
"cdna_end": null,
"cdna_length": 7178,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1714G>A",
"hgvs_p": "p.Gly572Arg",
"transcript": "ENST00000650560.1",
"protein_id": "ENSP00000497816.1",
"transcript_support_level": null,
"aa_start": 572,
"aa_end": null,
"aa_length": 1185,
"cds_start": 1714,
"cds_end": null,
"cds_length": 3558,
"cdna_start": 2525,
"cdna_end": null,
"cdna_length": 7067,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1711G>A",
"hgvs_p": "p.Gly571Arg",
"transcript": "NM_001329847.2",
"protein_id": "NP_001316776.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1184,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3555,
"cdna_start": 2507,
"cdna_end": null,
"cdna_length": 7105,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1711G>A",
"hgvs_p": "p.Gly571Arg",
"transcript": "NM_001329848.1",
"protein_id": "NP_001316777.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1184,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3555,
"cdna_start": 2589,
"cdna_end": null,
"cdna_length": 7187,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1711G>A",
"hgvs_p": "p.Gly571Arg",
"transcript": "NM_015025.4",
"protein_id": "NP_055840.2",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1184,
"cds_start": 1711,
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"cdna_start": 2540,
"cdna_end": null,
"cdna_length": 7138,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1711G>A",
"hgvs_p": "p.Gly571Arg",
"transcript": "ENST00000648316.1",
"protein_id": "ENSP00000497870.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1184,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3555,
"cdna_start": 2665,
"cdna_end": null,
"cdna_length": 6912,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1711G>A",
"hgvs_p": "p.Gly571Arg",
"transcript": "ENST00000648928.1",
"protein_id": "ENSP00000497017.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1184,
"cds_start": 1711,
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"cdna_start": 2750,
"cdna_end": null,
"cdna_length": 7322,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1711G>A",
"hgvs_p": "p.Gly571Arg",
"transcript": "ENST00000649207.1",
"protein_id": "ENSP00000496986.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1184,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3555,
"cdna_start": 2612,
"cdna_end": null,
"cdna_length": 7009,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1711G>A",
"hgvs_p": "p.Gly571Arg",
"transcript": "NM_001329849.3",
"protein_id": "NP_001316778.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1148,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3447,
"cdna_start": 2540,
"cdna_end": null,
"cdna_length": 6376,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1711G>A",
"hgvs_p": "p.Gly571Arg",
"transcript": "ENST00000648665.2",
"protein_id": "ENSP00000497115.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1711G>A",
"hgvs_p": "p.Gly571Arg",
"transcript": "NM_001329846.3",
"protein_id": "NP_001316775.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1146,
"cds_start": 1711,
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"cdna_start": 2507,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "G",
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1711G>A",
"hgvs_p": "p.Gly571Arg",
"transcript": "ENST00000647755.1",
"protein_id": "ENSP00000496922.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1146,
"cds_start": 1711,
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"cds_length": 3441,
"cdna_start": 2406,
"cdna_end": null,
"cdna_length": 6259,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MYT1L",
"gene_hgnc_id": 7623,
"hgvs_c": "c.1717G>A",
"hgvs_p": "p.Gly573Arg",
"transcript": "NM_001329851.3",
"protein_id": "NP_001316780.1",
"transcript_support_level": null,
"aa_start": 573,
"aa_end": null,
"aa_length": 1143,
"cds_start": 1717,
"cds_end": null,
"cds_length": 3432,
"cdna_start": 2546,
"cdna_end": null,
"cdna_length": 7434,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
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"computational_score_selected": 0.950414776802063,
"computational_prediction_selected": "Pathogenic",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.029999999329447746,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.832,
"revel_prediction": "Pathogenic",
"alphamissense_score": 0.9998,
"alphamissense_prediction": null,
"bayesdelnoaf_score": 0.3,
"bayesdelnoaf_prediction": "Pathogenic",
"phylop100way_score": 7.813,
"phylop100way_prediction": "Pathogenic",
"spliceai_max_score": 0.03,
"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": 9,
"acmg_classification": "Likely_pathogenic",
"acmg_criteria": "PM2,PM5,PP3_Strong,PP5",
"acmg_by_gene": [
{
"score": 9,
"benign_score": 0,
"pathogenic_score": 9,
"criteria": [
"PM2",
"PM5",
"PP3_Strong",
"PP5"
],
"verdict": "Likely_pathogenic",
"transcript": "ENST00000647738.2",
"gene_symbol": "MYT1L",
"hgnc_id": 7623,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.1717G>A",
"hgvs_p": "p.Gly573Arg"
}
],
"clinvar_disease": " autosomal dominant 39,Inborn genetic diseases,Intellectual disability,not provided",
"clinvar_classification": "Conflicting classifications of pathogenicity",
"clinvar_review_status": "criteria provided, conflicting classifications",
"clinvar_submissions_summary": "P:1 LP:2 US:1",
"phenotype_combined": "Inborn genetic diseases|not provided|Intellectual disability, autosomal dominant 39",
"pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
"custom_annotations": null
}
],
"message": null
}