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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: 7-36522062-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=36522062&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "7",
      "pos": 36522062,
      "ref": "C",
      "alt": "T",
      "effect": "missense_variant",
      "transcript": "NM_001637.4",
      "consequences": [
        {
          "aa_ref": "V",
          "aa_alt": "M",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "AOAH",
          "gene_hgnc_id": 548,
          "hgvs_c": "c.1576G>A",
          "hgvs_p": "p.Val526Met",
          "transcript": "NM_001637.4",
          "protein_id": "NP_001628.1",
          "transcript_support_level": null,
          "aa_start": 526,
          "aa_end": null,
          "aa_length": 575,
          "cds_start": 1576,
          "cds_end": null,
          "cds_length": 1728,
          "cdna_start": 1922,
          "cdna_end": null,
          "cdna_length": 2385,
          "mane_select": "ENST00000617537.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "M",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "AOAH",
          "gene_hgnc_id": 548,
          "hgvs_c": "c.1576G>A",
          "hgvs_p": "p.Val526Met",
          "transcript": "ENST00000617537.5",
          "protein_id": "ENSP00000483783.1",
          "transcript_support_level": 1,
          "aa_start": 526,
          "aa_end": null,
          "aa_length": 575,
          "cds_start": 1576,
          "cds_end": null,
          "cds_length": 1728,
          "cdna_start": 1922,
          "cdna_end": null,
          "cdna_length": 2385,
          "mane_select": "NM_001637.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "M",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "AOAH",
          "gene_hgnc_id": 548,
          "hgvs_c": "c.1576G>A",
          "hgvs_p": "p.Val526Met",
          "transcript": "ENST00000617267.5",
          "protein_id": "ENSP00000479664.1",
          "transcript_support_level": 1,
          "aa_start": 526,
          "aa_end": null,
          "aa_length": 688,
          "cds_start": 1576,
          "cds_end": null,
          "cds_length": 2067,
          "cdna_start": 1877,
          "cdna_end": null,
          "cdna_length": 6092,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "M",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "AOAH",
          "gene_hgnc_id": 548,
          "hgvs_c": "c.1576G>A",
          "hgvs_p": "p.Val526Met",
          "transcript": "NM_001177506.2",
          "protein_id": "NP_001170977.1",
          "transcript_support_level": null,
          "aa_start": 526,
          "aa_end": null,
          "aa_length": 688,
          "cds_start": 1576,
          "cds_end": null,
          "cds_length": 2067,
          "cdna_start": 1922,
          "cdna_end": null,
          "cdna_length": 2504,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "M",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "AOAH",
          "gene_hgnc_id": 548,
          "hgvs_c": "c.1480G>A",
          "hgvs_p": "p.Val494Met",
          "transcript": "NM_001177507.2",
          "protein_id": "NP_001170978.1",
          "transcript_support_level": null,
          "aa_start": 494,
          "aa_end": null,
          "aa_length": 543,
          "cds_start": 1480,
          "cds_end": null,
          "cds_length": 1632,
          "cdna_start": 1826,
          "cdna_end": null,
          "cdna_length": 2289,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "M",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "AOAH",
          "gene_hgnc_id": 548,
          "hgvs_c": "c.1480G>A",
          "hgvs_p": "p.Val494Met",
          "transcript": "ENST00000612871.4",
          "protein_id": "ENSP00000484305.1",
          "transcript_support_level": 2,
          "aa_start": 494,
          "aa_end": null,
          "aa_length": 543,
          "cds_start": 1480,
          "cds_end": null,
          "cds_length": 1632,
          "cdna_start": 1881,
          "cdna_end": null,
          "cdna_length": 2336,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "M",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "AOAH",
          "gene_hgnc_id": 548,
          "hgvs_c": "c.1501G>A",
          "hgvs_p": "p.Val501Met",
          "transcript": "XM_011515333.3",
          "protein_id": "XP_011513635.1",
          "transcript_support_level": null,
          "aa_start": 501,
          "aa_end": null,
          "aa_length": 663,
          "cds_start": 1501,
          "cds_end": null,
          "cds_length": 1992,
          "cdna_start": 1847,
          "cdna_end": null,
          "cdna_length": 2429,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "M",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "AOAH",
          "gene_hgnc_id": 548,
          "hgvs_c": "c.1480G>A",
          "hgvs_p": "p.Val494Met",
          "transcript": "XM_011515334.3",
          "protein_id": "XP_011513636.1",
          "transcript_support_level": null,
          "aa_start": 494,
          "aa_end": null,
          "aa_length": 656,
          "cds_start": 1480,
          "cds_end": null,
          "cds_length": 1971,
          "cdna_start": 1826,
          "cdna_end": null,
          "cdna_length": 2408,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "M",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "AOAH",
          "gene_hgnc_id": 548,
          "hgvs_c": "c.1453G>A",
          "hgvs_p": "p.Val485Met",
          "transcript": "XM_011515335.3",
          "protein_id": "XP_011513637.1",
          "transcript_support_level": null,
          "aa_start": 485,
          "aa_end": null,
          "aa_length": 647,
          "cds_start": 1453,
          "cds_end": null,
          "cds_length": 1944,
          "cdna_start": 2006,
          "cdna_end": null,
          "cdna_length": 2588,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "M",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "AOAH",
          "gene_hgnc_id": 548,
          "hgvs_c": "c.1576G>A",
          "hgvs_p": "p.Val526Met",
          "transcript": "XM_011515336.3",
          "protein_id": "XP_011513638.1",
          "transcript_support_level": null,
          "aa_start": 526,
          "aa_end": null,
          "aa_length": 572,
          "cds_start": 1576,
          "cds_end": null,
          "cds_length": 1719,
          "cdna_start": 1922,
          "cdna_end": null,
          "cdna_length": 2506,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "M",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "AOAH",
          "gene_hgnc_id": 548,
          "hgvs_c": "c.1576G>A",
          "hgvs_p": "p.Val526Met",
          "transcript": "XM_047420297.1",
          "protein_id": "XP_047276253.1",
          "transcript_support_level": null,
          "aa_start": 526,
          "aa_end": null,
          "aa_length": 566,
          "cds_start": 1576,
          "cds_end": null,
          "cds_length": 1701,
          "cdna_start": 1922,
          "cdna_end": null,
          "cdna_length": 2181,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "M",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "AOAH",
          "gene_hgnc_id": 548,
          "hgvs_c": "c.1501G>A",
          "hgvs_p": "p.Val501Met",
          "transcript": "XM_017012102.3",
          "protein_id": "XP_016867591.1",
          "transcript_support_level": null,
          "aa_start": 501,
          "aa_end": null,
          "aa_length": 550,
          "cds_start": 1501,
          "cds_end": null,
          "cds_length": 1653,
          "cdna_start": 1847,
          "cdna_end": null,
          "cdna_length": 2310,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "M",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "AOAH",
          "gene_hgnc_id": 548,
          "hgvs_c": "c.1576G>A",
          "hgvs_p": "p.Val526Met",
          "transcript": "XM_011515338.3",
          "protein_id": "XP_011513640.1",
          "transcript_support_level": null,
          "aa_start": 526,
          "aa_end": null,
          "aa_length": 534,
          "cds_start": 1576,
          "cds_end": null,
          "cds_length": 1605,
          "cdna_start": 1922,
          "cdna_end": null,
          "cdna_length": 1969,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "M",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "AOAH",
          "gene_hgnc_id": 548,
          "hgvs_c": "c.1501G>A",
          "hgvs_p": "p.Val501Met",
          "transcript": "XM_017012104.1",
          "protein_id": "XP_016867593.1",
          "transcript_support_level": null,
          "aa_start": 501,
          "aa_end": null,
          "aa_length": 509,
          "cds_start": 1501,
          "cds_end": null,
          "cds_length": 1530,
          "cdna_start": 1847,
          "cdna_end": null,
          "cdna_length": 1986,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "M",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "AOAH",
          "gene_hgnc_id": 548,
          "hgvs_c": "c.883G>A",
          "hgvs_p": "p.Val295Met",
          "transcript": "XM_017012105.2",
          "protein_id": "XP_016867594.1",
          "transcript_support_level": null,
          "aa_start": 295,
          "aa_end": null,
          "aa_length": 457,
          "cds_start": 883,
          "cds_end": null,
          "cds_length": 1374,
          "cdna_start": 1037,
          "cdna_end": null,
          "cdna_length": 1619,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "M",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "AOAH",
          "gene_hgnc_id": 548,
          "hgvs_c": "c.745G>A",
          "hgvs_p": "p.Val249Met",
          "transcript": "XM_011515342.3",
          "protein_id": "XP_011513644.1",
          "transcript_support_level": null,
          "aa_start": 249,
          "aa_end": null,
          "aa_length": 411,
          "cds_start": 745,
          "cds_end": null,
          "cds_length": 1236,
          "cdna_start": 877,
          "cdna_end": null,
          "cdna_length": 1459,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "AOAH",
          "gene_hgnc_id": 548,
          "hgvs_c": "n.321G>A",
          "hgvs_p": null,
          "transcript": "ENST00000614254.1",
          "protein_id": null,
          "transcript_support_level": 2,
          "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": 722,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "AOAH",
      "gene_hgnc_id": 548,
      "dbsnp": "rs896206611",
      "frequency_reference_population": 0.000008054144,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 13,
      "gnomad_exomes_af": 0.00000478843,
      "gnomad_genomes_af": 0.0000394166,
      "gnomad_exomes_ac": 7,
      "gnomad_genomes_ac": 6,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.48389777541160583,
      "computational_prediction_selected": "Uncertain_significance",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.178,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.2068,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.11,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 1.356,
      "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": "Uncertain_significance",
      "acmg_criteria": "PM2",
      "acmg_by_gene": [
        {
          "score": 2,
          "benign_score": 0,
          "pathogenic_score": 2,
          "criteria": [
            "PM2"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "NM_001637.4",
          "gene_symbol": "AOAH",
          "hgnc_id": 548,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.1576G>A",
          "hgvs_p": "p.Val526Met"
        }
      ],
      "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
}