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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: 14-94464807-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=94464807&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "14",
"pos": 94464807,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_175739.4",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.950A>G",
"hgvs_p": "p.Asn317Ser",
"transcript": "NM_175739.4",
"protein_id": "NP_783866.3",
"transcript_support_level": null,
"aa_start": 317,
"aa_end": null,
"aa_length": 417,
"cds_start": 950,
"cds_end": null,
"cds_length": 1254,
"cdna_start": 1029,
"cdna_end": null,
"cdna_length": 1705,
"mane_select": "ENST00000674397.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_175739.4"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.950A>G",
"hgvs_p": "p.Asn317Ser",
"transcript": "ENST00000674397.2",
"protein_id": "ENSP00000501517.1",
"transcript_support_level": null,
"aa_start": 317,
"aa_end": null,
"aa_length": 417,
"cds_start": 950,
"cds_end": null,
"cds_length": 1254,
"cdna_start": 1029,
"cdna_end": null,
"cdna_length": 1705,
"mane_select": "NM_175739.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000674397.2"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.1004A>G",
"hgvs_p": "p.Asn335Ser",
"transcript": "ENST00000337425.10",
"protein_id": "ENSP00000337133.5",
"transcript_support_level": 1,
"aa_start": 335,
"aa_end": null,
"aa_length": 435,
"cds_start": 1004,
"cds_end": null,
"cds_length": 1308,
"cdna_start": 1165,
"cdna_end": null,
"cdna_length": 1839,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000337425.10"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.710A>G",
"hgvs_p": "p.Asn237Ser",
"transcript": "ENST00000448305.6",
"protein_id": "ENSP00000414092.2",
"transcript_support_level": 1,
"aa_start": 237,
"aa_end": null,
"aa_length": 337,
"cds_start": 710,
"cds_end": null,
"cds_length": 1014,
"cdna_start": 840,
"cdna_end": null,
"cdna_length": 1520,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000448305.6"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.650A>G",
"hgvs_p": "p.Asn217Ser",
"transcript": "ENST00000298845.12",
"protein_id": "ENSP00000298845.8",
"transcript_support_level": 1,
"aa_start": 217,
"aa_end": null,
"aa_length": 317,
"cds_start": 650,
"cds_end": null,
"cds_length": 954,
"cdna_start": 743,
"cdna_end": null,
"cdna_length": 1423,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000298845.12"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.557A>G",
"hgvs_p": "p.Asn186Ser",
"transcript": "ENST00000424550.6",
"protein_id": "ENSP00000409012.2",
"transcript_support_level": 1,
"aa_start": 186,
"aa_end": null,
"aa_length": 286,
"cds_start": 557,
"cds_end": null,
"cds_length": 861,
"cdna_start": 782,
"cdna_end": null,
"cdna_length": 1462,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000424550.6"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.710A>G",
"hgvs_p": "p.Asn237Ser",
"transcript": "ENST00000546329.2",
"protein_id": "ENSP00000445476.2",
"transcript_support_level": 1,
"aa_start": 237,
"aa_end": null,
"aa_length": 272,
"cds_start": 710,
"cds_end": null,
"cds_length": 819,
"cdna_start": 975,
"cdna_end": null,
"cdna_length": 1156,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000546329.2"
},
{
"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": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "n.*480A>G",
"hgvs_p": null,
"transcript": "ENST00000538527.5",
"protein_id": "ENSP00000441511.1",
"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": 1346,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000538527.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "n.*480A>G",
"hgvs_p": null,
"transcript": "ENST00000538527.5",
"protein_id": "ENSP00000441511.1",
"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": 1346,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000538527.5"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.974A>G",
"hgvs_p": "p.Asn325Ser",
"transcript": "ENST00000853990.1",
"protein_id": "ENSP00000524049.1",
"transcript_support_level": null,
"aa_start": 325,
"aa_end": null,
"aa_length": 425,
"cds_start": 974,
"cds_end": null,
"cds_length": 1278,
"cdna_start": 1080,
"cdna_end": null,
"cdna_length": 1740,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000853990.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.950A>G",
"hgvs_p": "p.Asn317Ser",
"transcript": "ENST00000380365.7",
"protein_id": "ENSP00000369723.3",
"transcript_support_level": 5,
"aa_start": 317,
"aa_end": null,
"aa_length": 417,
"cds_start": 950,
"cds_end": null,
"cds_length": 1254,
"cdna_start": 1029,
"cdna_end": null,
"cdna_length": 1333,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000380365.7"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.950A>G",
"hgvs_p": "p.Asn317Ser",
"transcript": "ENST00000853989.1",
"protein_id": "ENSP00000524048.1",
"transcript_support_level": null,
"aa_start": 317,
"aa_end": null,
"aa_length": 417,
"cds_start": 950,
"cds_end": null,
"cds_length": 1254,
"cdna_start": 1189,
"cdna_end": null,
"cdna_length": 1863,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000853989.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.710A>G",
"hgvs_p": "p.Asn237Ser",
"transcript": "NM_001284275.2",
"protein_id": "NP_001271204.2",
"transcript_support_level": null,
"aa_start": 237,
"aa_end": null,
"aa_length": 337,
"cds_start": 710,
"cds_end": null,
"cds_length": 1014,
"cdna_start": 839,
"cdna_end": null,
"cdna_length": 1515,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001284275.2"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.704A>G",
"hgvs_p": "p.Asn235Ser",
"transcript": "ENST00000674164.1",
"protein_id": "ENSP00000501328.1",
"transcript_support_level": null,
"aa_start": 235,
"aa_end": null,
"aa_length": 335,
"cds_start": 704,
"cds_end": null,
"cds_length": 1008,
"cdna_start": 865,
"cdna_end": null,
"cdna_length": 1539,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000674164.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.650A>G",
"hgvs_p": "p.Asn217Ser",
"transcript": "NM_001042518.2",
"protein_id": "NP_001035983.2",
"transcript_support_level": null,
"aa_start": 217,
"aa_end": null,
"aa_length": 317,
"cds_start": 650,
"cds_end": null,
"cds_length": 954,
"cdna_start": 729,
"cdna_end": null,
"cdna_length": 1405,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001042518.2"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.557A>G",
"hgvs_p": "p.Asn186Ser",
"transcript": "NM_001284276.2",
"protein_id": "NP_001271205.1",
"transcript_support_level": null,
"aa_start": 186,
"aa_end": null,
"aa_length": 286,
"cds_start": 557,
"cds_end": null,
"cds_length": 861,
"cdna_start": 736,
"cdna_end": null,
"cdna_length": 1412,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001284276.2"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.950A>G",
"hgvs_p": "p.Asn317Ser",
"transcript": "XM_011536714.3",
"protein_id": "XP_011535016.1",
"transcript_support_level": null,
"aa_start": 317,
"aa_end": null,
"aa_length": 417,
"cds_start": 950,
"cds_end": null,
"cds_length": 1254,
"cdna_start": 1241,
"cdna_end": null,
"cdna_length": 1917,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011536714.3"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.950A>G",
"hgvs_p": "p.Asn317Ser",
"transcript": "XM_011536715.3",
"protein_id": "XP_011535017.1",
"transcript_support_level": null,
"aa_start": 317,
"aa_end": null,
"aa_length": 417,
"cds_start": 950,
"cds_end": null,
"cds_length": 1254,
"cdna_start": 1127,
"cdna_end": null,
"cdna_length": 1803,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011536715.3"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.950A>G",
"hgvs_p": "p.Asn317Ser",
"transcript": "XM_047431339.1",
"protein_id": "XP_047287295.1",
"transcript_support_level": null,
"aa_start": 317,
"aa_end": null,
"aa_length": 417,
"cds_start": 950,
"cds_end": null,
"cds_length": 1254,
"cdna_start": 2216,
"cdna_end": null,
"cdna_length": 2892,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047431339.1"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.710A>G",
"hgvs_p": "p.Asn237Ser",
"transcript": "XM_011536716.3",
"protein_id": "XP_011535018.1",
"transcript_support_level": null,
"aa_start": 237,
"aa_end": null,
"aa_length": 337,
"cds_start": 710,
"cds_end": null,
"cds_length": 1014,
"cdna_start": 1051,
"cdna_end": null,
"cdna_length": 1727,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011536716.3"
},
{
"aa_ref": "N",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"hgvs_c": "c.710A>G",
"hgvs_p": "p.Asn237Ser",
"transcript": "XM_047431341.1",
"protein_id": "XP_047287297.1",
"transcript_support_level": null,
"aa_start": 237,
"aa_end": null,
"aa_length": 337,
"cds_start": 710,
"cds_end": null,
"cds_length": 1014,
"cdna_start": 2026,
"cdna_end": null,
"cdna_length": 2702,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047431341.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"downstream_gene_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ENSG00000256357",
"gene_hgnc_id": null,
"hgvs_c": "n.*77T>C",
"hgvs_p": null,
"transcript": "ENST00000536735.1",
"protein_id": null,
"transcript_support_level": 4,
"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": 568,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000536735.1"
}
],
"gene_symbol": "SERPINA9",
"gene_hgnc_id": 15995,
"dbsnp": "rs769429068",
"frequency_reference_population": 0.000028506836,
"hom_count_reference_population": 0,
"allele_count_reference_population": 46,
"gnomad_exomes_af": 0.0000294236,
"gnomad_genomes_af": 0.0000197062,
"gnomad_exomes_ac": 43,
"gnomad_genomes_ac": 3,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.22168707847595215,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0.36000001430511475,
"splice_prediction_selected": "Uncertain_significance",
"splice_source_selected": "max_spliceai",
"revel_score": 0.289,
"revel_prediction": "Benign",
"alphamissense_score": 0.0833,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.47,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 3.783,
"phylop100way_prediction": "Uncertain_significance",
"spliceai_max_score": 0.36,
"spliceai_max_prediction": "Uncertain_significance",
"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": "",
"acmg_by_gene": [
{
"score": 0,
"benign_score": 0,
"pathogenic_score": 0,
"criteria": [],
"verdict": "Uncertain_significance",
"transcript": "NM_175739.4",
"gene_symbol": "SERPINA9",
"hgnc_id": 15995,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.950A>G",
"hgvs_p": "p.Asn317Ser"
},
{
"score": 0,
"benign_score": 0,
"pathogenic_score": 0,
"criteria": [],
"verdict": "Uncertain_significance",
"transcript": "ENST00000536735.1",
"gene_symbol": "ENSG00000256357",
"hgnc_id": null,
"effects": [
"downstream_gene_variant"
],
"inheritance_mode": "",
"hgvs_c": "n.*77T>C",
"hgvs_p": null
}
],
"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
}