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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: 1-107574079-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=107574079&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 107574079,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_006113.5",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VAV3",
"gene_hgnc_id": 12659,
"hgvs_c": "c.2470A>G",
"hgvs_p": "p.Asn824Asp",
"transcript": "NM_006113.5",
"protein_id": "NP_006104.4",
"transcript_support_level": null,
"aa_start": 824,
"aa_end": null,
"aa_length": 847,
"cds_start": 2470,
"cds_end": null,
"cds_length": 2544,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000370056.9",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_006113.5"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VAV3",
"gene_hgnc_id": 12659,
"hgvs_c": "c.2470A>G",
"hgvs_p": "p.Asn824Asp",
"transcript": "ENST00000370056.9",
"protein_id": "ENSP00000359073.4",
"transcript_support_level": 1,
"aa_start": 824,
"aa_end": null,
"aa_length": 847,
"cds_start": 2470,
"cds_end": null,
"cds_length": 2544,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_006113.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000370056.9"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VAV3",
"gene_hgnc_id": 12659,
"hgvs_c": "c.2554A>G",
"hgvs_p": "p.Asn852Asp",
"transcript": "ENST00000527011.5",
"protein_id": "ENSP00000432540.1",
"transcript_support_level": 1,
"aa_start": 852,
"aa_end": null,
"aa_length": 875,
"cds_start": 2554,
"cds_end": null,
"cds_length": 2628,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000527011.5"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VAV3",
"gene_hgnc_id": 12659,
"hgvs_c": "c.790A>G",
"hgvs_p": "p.Asn264Asp",
"transcript": "ENST00000415432.6",
"protein_id": "ENSP00000394897.2",
"transcript_support_level": 1,
"aa_start": 264,
"aa_end": null,
"aa_length": 287,
"cds_start": 790,
"cds_end": null,
"cds_length": 864,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000415432.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VAV3",
"gene_hgnc_id": 12659,
"hgvs_c": "n.2316A>G",
"hgvs_p": null,
"transcript": "ENST00000343258.8",
"protein_id": null,
"transcript_support_level": 1,
"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": "ENST00000343258.8"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VAV3",
"gene_hgnc_id": 12659,
"hgvs_c": "c.2524A>G",
"hgvs_p": "p.Asn842Asp",
"transcript": "ENST00000923907.1",
"protein_id": "ENSP00000593966.1",
"transcript_support_level": null,
"aa_start": 842,
"aa_end": null,
"aa_length": 865,
"cds_start": 2524,
"cds_end": null,
"cds_length": 2598,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000923907.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VAV3",
"gene_hgnc_id": 12659,
"hgvs_c": "c.790A>G",
"hgvs_p": "p.Asn264Asp",
"transcript": "NM_001079874.2",
"protein_id": "NP_001073343.1",
"transcript_support_level": null,
"aa_start": 264,
"aa_end": null,
"aa_length": 287,
"cds_start": 790,
"cds_end": null,
"cds_length": 864,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001079874.2"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VAV3",
"gene_hgnc_id": 12659,
"hgvs_c": "c.2398A>G",
"hgvs_p": "p.Asn800Asp",
"transcript": "XM_017000053.2",
"protein_id": "XP_016855542.1",
"transcript_support_level": null,
"aa_start": 800,
"aa_end": null,
"aa_length": 823,
"cds_start": 2398,
"cds_end": null,
"cds_length": 2472,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017000053.2"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VAV3",
"gene_hgnc_id": 12659,
"hgvs_c": "c.2209A>G",
"hgvs_p": "p.Asn737Asp",
"transcript": "XM_024450319.2",
"protein_id": "XP_024306087.1",
"transcript_support_level": null,
"aa_start": 737,
"aa_end": null,
"aa_length": 760,
"cds_start": 2209,
"cds_end": null,
"cds_length": 2283,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_024450319.2"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VAV3",
"gene_hgnc_id": 12659,
"hgvs_c": "c.2188A>G",
"hgvs_p": "p.Asn730Asp",
"transcript": "XM_005270360.3",
"protein_id": "XP_005270417.1",
"transcript_support_level": null,
"aa_start": 730,
"aa_end": null,
"aa_length": 753,
"cds_start": 2188,
"cds_end": null,
"cds_length": 2262,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_005270360.3"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VAV3",
"gene_hgnc_id": 12659,
"hgvs_c": "c.2182A>G",
"hgvs_p": "p.Asn728Asp",
"transcript": "XM_017000055.1",
"protein_id": "XP_016855544.1",
"transcript_support_level": null,
"aa_start": 728,
"aa_end": null,
"aa_length": 751,
"cds_start": 2182,
"cds_end": null,
"cds_length": 2256,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017000055.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VAV3",
"gene_hgnc_id": 12659,
"hgvs_c": "c.1942A>G",
"hgvs_p": "p.Asn648Asp",
"transcript": "XM_047430439.1",
"protein_id": "XP_047286395.1",
"transcript_support_level": null,
"aa_start": 648,
"aa_end": null,
"aa_length": 671,
"cds_start": 1942,
"cds_end": null,
"cds_length": 2016,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047430439.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VAV3",
"gene_hgnc_id": 12659,
"hgvs_c": "c.1942A>G",
"hgvs_p": "p.Asn648Asp",
"transcript": "XM_047430476.1",
"protein_id": "XP_047286432.1",
"transcript_support_level": null,
"aa_start": 648,
"aa_end": null,
"aa_length": 671,
"cds_start": 1942,
"cds_end": null,
"cds_length": 2016,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047430476.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VAV3",
"gene_hgnc_id": 12659,
"hgvs_c": "c.1150A>G",
"hgvs_p": "p.Asn384Asp",
"transcript": "XM_017000056.2",
"protein_id": "XP_016855545.1",
"transcript_support_level": null,
"aa_start": 384,
"aa_end": null,
"aa_length": 407,
"cds_start": 1150,
"cds_end": null,
"cds_length": 1224,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017000056.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VAV3",
"gene_hgnc_id": 12659,
"hgvs_c": "n.968A>G",
"hgvs_p": null,
"transcript": "ENST00000525460.5",
"protein_id": null,
"transcript_support_level": 2,
"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": "ENST00000525460.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VAV3",
"gene_hgnc_id": 12659,
"hgvs_c": "n.*585A>G",
"hgvs_p": null,
"transcript": "ENST00000529413.5",
"protein_id": "ENSP00000432865.1",
"transcript_support_level": 2,
"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": "nonsense_mediated_decay",
"feature": "ENST00000529413.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "VAV3",
"gene_hgnc_id": 12659,
"hgvs_c": "n.*585A>G",
"hgvs_p": null,
"transcript": "ENST00000529413.5",
"protein_id": "ENSP00000432865.1",
"transcript_support_level": 2,
"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": "nonsense_mediated_decay",
"feature": "ENST00000529413.5"
}
],
"gene_symbol": "VAV3",
"gene_hgnc_id": 12659,
"dbsnp": "rs1649444919",
"frequency_reference_population": 0.0000018587821,
"hom_count_reference_population": 0,
"allele_count_reference_population": 3,
"gnomad_exomes_af": 6.84069e-7,
"gnomad_genomes_af": 0.0000131475,
"gnomad_exomes_ac": 1,
"gnomad_genomes_ac": 2,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.230142742395401,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.172,
"revel_prediction": "Benign",
"alphamissense_score": 0.3503,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.47,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 5.127,
"phylop100way_prediction": "Uncertain_significance",
"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_006113.5",
"gene_symbol": "VAV3",
"hgnc_id": 12659,
"effects": [
"missense_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.2470A>G",
"hgvs_p": "p.Asn824Asp"
}
],
"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
}