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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: 12-49598760-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=49598760&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 49598760,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_032130.3",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FAM186B",
"gene_hgnc_id": 25296,
"hgvs_c": "c.2359C>G",
"hgvs_p": "p.Pro787Ala",
"transcript": "NM_032130.3",
"protein_id": "NP_115506.1",
"transcript_support_level": null,
"aa_start": 787,
"aa_end": null,
"aa_length": 893,
"cds_start": 2359,
"cds_end": null,
"cds_length": 2682,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000257894.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_032130.3"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FAM186B",
"gene_hgnc_id": 25296,
"hgvs_c": "c.2359C>G",
"hgvs_p": "p.Pro787Ala",
"transcript": "ENST00000257894.2",
"protein_id": "ENSP00000257894.2",
"transcript_support_level": 1,
"aa_start": 787,
"aa_end": null,
"aa_length": 893,
"cds_start": 2359,
"cds_end": null,
"cds_length": 2682,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_032130.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000257894.2"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FAM186B",
"gene_hgnc_id": 25296,
"hgvs_c": "c.1198C>G",
"hgvs_p": "p.Pro400Ala",
"transcript": "ENST00000532262.5",
"protein_id": "ENSP00000436995.1",
"transcript_support_level": 1,
"aa_start": 400,
"aa_end": null,
"aa_length": 506,
"cds_start": 1198,
"cds_end": null,
"cds_length": 1521,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000532262.5"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 1,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FAM186B",
"gene_hgnc_id": 25296,
"hgvs_c": "c.28C>G",
"hgvs_p": "p.Pro10Ala",
"transcript": "ENST00000548841.5",
"protein_id": "ENSP00000448989.1",
"transcript_support_level": 5,
"aa_start": 10,
"aa_end": null,
"aa_length": 116,
"cds_start": 28,
"cds_end": null,
"cds_length": 351,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000548841.5"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FAM186B",
"gene_hgnc_id": 25296,
"hgvs_c": "c.2359C>G",
"hgvs_p": "p.Pro787Ala",
"transcript": "XM_006719625.3",
"protein_id": "XP_006719688.1",
"transcript_support_level": null,
"aa_start": 787,
"aa_end": null,
"aa_length": 893,
"cds_start": 2359,
"cds_end": null,
"cds_length": 2682,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006719625.3"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FAM186B",
"gene_hgnc_id": 25296,
"hgvs_c": "c.2359C>G",
"hgvs_p": "p.Pro787Ala",
"transcript": "XM_011538796.3",
"protein_id": "XP_011537098.1",
"transcript_support_level": null,
"aa_start": 787,
"aa_end": null,
"aa_length": 893,
"cds_start": 2359,
"cds_end": null,
"cds_length": 2682,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011538796.3"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FAM186B",
"gene_hgnc_id": 25296,
"hgvs_c": "c.2359C>G",
"hgvs_p": "p.Pro787Ala",
"transcript": "XM_006719626.3",
"protein_id": "XP_006719689.1",
"transcript_support_level": null,
"aa_start": 787,
"aa_end": null,
"aa_length": 871,
"cds_start": 2359,
"cds_end": null,
"cds_length": 2616,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006719626.3"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FAM186B",
"gene_hgnc_id": 25296,
"hgvs_c": "c.2359C>G",
"hgvs_p": "p.Pro787Ala",
"transcript": "XM_006719627.4",
"protein_id": "XP_006719690.1",
"transcript_support_level": null,
"aa_start": 787,
"aa_end": null,
"aa_length": 862,
"cds_start": 2359,
"cds_end": null,
"cds_length": 2589,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_006719627.4"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FAM186B",
"gene_hgnc_id": 25296,
"hgvs_c": "c.2089C>G",
"hgvs_p": "p.Pro697Ala",
"transcript": "XM_047429639.1",
"protein_id": "XP_047285595.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 803,
"cds_start": 2089,
"cds_end": null,
"cds_length": 2412,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047429639.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FAM186B",
"gene_hgnc_id": 25296,
"hgvs_c": "c.2089C>G",
"hgvs_p": "p.Pro697Ala",
"transcript": "XM_047429640.1",
"protein_id": "XP_047285596.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 803,
"cds_start": 2089,
"cds_end": null,
"cds_length": 2412,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047429640.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FAM186B",
"gene_hgnc_id": 25296,
"hgvs_c": "c.2089C>G",
"hgvs_p": "p.Pro697Ala",
"transcript": "XM_047429641.1",
"protein_id": "XP_047285597.1",
"transcript_support_level": null,
"aa_start": 697,
"aa_end": null,
"aa_length": 803,
"cds_start": 2089,
"cds_end": null,
"cds_length": 2412,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047429641.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"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": "FAM186B",
"gene_hgnc_id": 25296,
"hgvs_c": "c.2359C>G",
"hgvs_p": "p.Pro787Ala",
"transcript": "XM_011538797.4",
"protein_id": "XP_011537099.1",
"transcript_support_level": null,
"aa_start": 787,
"aa_end": null,
"aa_length": 799,
"cds_start": 2359,
"cds_end": null,
"cds_length": 2400,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011538797.4"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "FAM186B",
"gene_hgnc_id": 25296,
"hgvs_c": "c.633+2247C>G",
"hgvs_p": null,
"transcript": "ENST00000551047.5",
"protein_id": "ENSP00000448656.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 241,
"cds_start": null,
"cds_end": null,
"cds_length": 726,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000551047.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PRPF40B",
"gene_hgnc_id": 25031,
"hgvs_c": "c.-161-23877G>C",
"hgvs_p": null,
"transcript": "ENST00000551063.5",
"protein_id": "ENSP00000449569.1",
"transcript_support_level": 4,
"aa_start": null,
"aa_end": null,
"aa_length": 5,
"cds_start": null,
"cds_end": null,
"cds_length": 18,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000551063.5"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FAM186B",
"gene_hgnc_id": 25296,
"hgvs_c": "n.*2365C>G",
"hgvs_p": null,
"transcript": "ENST00000533372.1",
"protein_id": "ENSP00000433047.1",
"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": "ENST00000533372.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FAM186B",
"gene_hgnc_id": 25296,
"hgvs_c": "n.2701C>G",
"hgvs_p": null,
"transcript": "NR_027450.2",
"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": "NR_027450.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "FAM186B",
"gene_hgnc_id": 25296,
"hgvs_c": "n.*2365C>G",
"hgvs_p": null,
"transcript": "ENST00000533372.1",
"protein_id": "ENSP00000433047.1",
"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": "ENST00000533372.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PRPF40B",
"gene_hgnc_id": 25031,
"hgvs_c": "n.188-5417G>C",
"hgvs_p": null,
"transcript": "ENST00000527253.2",
"protein_id": null,
"transcript_support_level": 3,
"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": "ENST00000527253.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 2,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PRPF40B",
"gene_hgnc_id": 25031,
"hgvs_c": "n.489-1068G>C",
"hgvs_p": null,
"transcript": "ENST00000547764.1",
"protein_id": null,
"transcript_support_level": 3,
"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": "ENST00000547764.1"
}
],
"gene_symbol": "FAM186B",
"gene_hgnc_id": 25296,
"dbsnp": "rs760921646",
"frequency_reference_population": 0.000016188102,
"hom_count_reference_population": 0,
"allele_count_reference_population": 26,
"gnomad_exomes_af": 0.0000171818,
"gnomad_genomes_af": 0.00000661875,
"gnomad_exomes_ac": 25,
"gnomad_genomes_ac": 1,
"gnomad_exomes_homalt": 0,
"gnomad_genomes_homalt": 0,
"gnomad_mito_homoplasmic": null,
"gnomad_mito_heteroplasmic": null,
"computational_score_selected": 0.1116911768913269,
"computational_prediction_selected": "Benign",
"computational_source_selected": "MetaRNN",
"splice_score_selected": 0,
"splice_prediction_selected": "Benign",
"splice_source_selected": "max_spliceai",
"revel_score": 0.191,
"revel_prediction": "Benign",
"alphamissense_score": 0.3228,
"alphamissense_prediction": null,
"bayesdelnoaf_score": -0.35,
"bayesdelnoaf_prediction": "Benign",
"phylop100way_score": 1.401,
"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": -2,
"acmg_classification": "Likely_benign",
"acmg_criteria": "BP4_Moderate",
"acmg_by_gene": [
{
"score": -2,
"benign_score": 2,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate"
],
"verdict": "Likely_benign",
"transcript": "NM_032130.3",
"gene_symbol": "FAM186B",
"hgnc_id": 25296,
"effects": [
"missense_variant"
],
"inheritance_mode": "AR",
"hgvs_c": "c.2359C>G",
"hgvs_p": "p.Pro787Ala"
},
{
"score": -6,
"benign_score": 6,
"pathogenic_score": 0,
"criteria": [
"BP4_Moderate",
"BS2"
],
"verdict": "Likely_benign",
"transcript": "ENST00000551063.5",
"gene_symbol": "PRPF40B",
"hgnc_id": 25031,
"effects": [
"intron_variant"
],
"inheritance_mode": "AD",
"hgvs_c": "c.-161-23877G>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
}