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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: 18-79377202-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=18&pos=79377202&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "18",
      "pos": 79377202,
      "ref": "A",
      "alt": "G",
      "effect": "intron_variant",
      "transcript": "NM_198531.5",
      "consequences": [
        {
          "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": 30,
          "intron_rank": 29,
          "intron_rank_end": null,
          "gene_symbol": "ATP9B",
          "gene_hgnc_id": 13541,
          "hgvs_c": "c.3308-45A>G",
          "hgvs_p": null,
          "transcript": "NM_198531.5",
          "protein_id": "NP_940933.3",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1147,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3444,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000426216.6",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_198531.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": 29,
          "intron_rank_end": null,
          "gene_symbol": "ATP9B",
          "gene_hgnc_id": 13541,
          "hgvs_c": "c.3308-45A>G",
          "hgvs_p": null,
          "transcript": "ENST00000426216.6",
          "protein_id": "ENSP00000398076.2",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1147,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3444,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_198531.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000426216.6"
        },
        {
          "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": 29,
          "intron_rank": 28,
          "intron_rank_end": null,
          "gene_symbol": "ATP9B",
          "gene_hgnc_id": 13541,
          "hgvs_c": "c.3275-45A>G",
          "hgvs_p": null,
          "transcript": "ENST00000307671.12",
          "protein_id": "ENSP00000304500.7",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1136,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3411,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000307671.12"
        },
        {
          "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": 8,
          "intron_rank": 7,
          "intron_rank_end": null,
          "gene_symbol": "ATP9B",
          "gene_hgnc_id": 13541,
          "hgvs_c": "n.*195-45A>G",
          "hgvs_p": null,
          "transcript": "ENST00000588921.1",
          "protein_id": "ENSP00000465269.1",
          "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": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000588921.1"
        },
        {
          "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": 31,
          "intron_rank": 30,
          "intron_rank_end": null,
          "gene_symbol": "ATP9B",
          "gene_hgnc_id": 13541,
          "hgvs_c": "c.3392-45A>G",
          "hgvs_p": null,
          "transcript": "ENST00000963364.1",
          "protein_id": "ENSP00000633423.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1175,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3528,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000963364.1"
        },
        {
          "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": 30,
          "intron_rank": 29,
          "intron_rank_end": null,
          "gene_symbol": "ATP9B",
          "gene_hgnc_id": 13541,
          "hgvs_c": "c.3386-45A>G",
          "hgvs_p": null,
          "transcript": "ENST00000899993.1",
          "protein_id": "ENSP00000570052.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1173,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3522,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000899993.1"
        },
        {
          "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": 29,
          "intron_rank": 28,
          "intron_rank_end": null,
          "gene_symbol": "ATP9B",
          "gene_hgnc_id": 13541,
          "hgvs_c": "c.3353-45A>G",
          "hgvs_p": null,
          "transcript": "ENST00000899989.1",
          "protein_id": "ENSP00000570048.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1162,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3489,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000899989.1"
        },
        {
          "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": 29,
          "intron_rank": 28,
          "intron_rank_end": null,
          "gene_symbol": "ATP9B",
          "gene_hgnc_id": 13541,
          "hgvs_c": "c.3305-45A>G",
          "hgvs_p": null,
          "transcript": "ENST00000963365.1",
          "protein_id": "ENSP00000633424.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1146,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3441,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000963365.1"
        },
        {
          "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": 29,
          "intron_rank": 28,
          "intron_rank_end": null,
          "gene_symbol": "ATP9B",
          "gene_hgnc_id": 13541,
          "hgvs_c": "c.3275-45A>G",
          "hgvs_p": null,
          "transcript": "NM_001306085.2",
          "protein_id": "NP_001293014.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1136,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3411,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001306085.2"
        },
        {
          "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": 29,
          "intron_rank": 28,
          "intron_rank_end": null,
          "gene_symbol": "ATP9B",
          "gene_hgnc_id": 13541,
          "hgvs_c": "c.3269-45A>G",
          "hgvs_p": null,
          "transcript": "ENST00000940834.1",
          "protein_id": "ENSP00000610893.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1134,
          "cds_start": null,
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          "cds_length": 3405,
          "cdna_start": null,
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          "mane_select": null,
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          "intron_rank": 27,
          "intron_rank_end": null,
          "gene_symbol": "ATP9B",
          "gene_hgnc_id": 13541,
          "hgvs_c": "c.3263-45A>G",
          "hgvs_p": null,
          "transcript": "ENST00000963369.1",
          "protein_id": "ENSP00000633428.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1132,
          "cds_start": null,
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          "cds_length": 3399,
          "cdna_start": null,
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          "mane_select": null,
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        {
          "aa_ref": null,
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          "canonical": false,
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          "gene_symbol": "ATP9B",
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          "cds_start": null,
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        {
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          "gene_symbol": "ATP9B",
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          "hgvs_c": "c.3254-45A>G",
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          "transcript": "ENST00000940836.1",
          "protein_id": "ENSP00000610895.1",
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        {
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          "intron_rank": 29,
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          "gene_symbol": "ATP9B",
          "gene_hgnc_id": 13541,
          "hgvs_c": "c.3245-45A>G",
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          "transcript": "ENST00000963370.1",
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        {
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        {
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          "intron_rank": 26,
          "intron_rank_end": null,
          "gene_symbol": "ATP9B",
          "gene_hgnc_id": 13541,
          "hgvs_c": "c.3164-45A>G",
          "hgvs_p": null,
          "transcript": "ENST00000963366.1",
          "protein_id": "ENSP00000633425.1",
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          "gene_symbol": "ATP9B",
          "gene_hgnc_id": 13541,
          "hgvs_c": "c.3152-45A>G",
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          "transcript": "ENST00000899991.1",
          "protein_id": "ENSP00000570050.1",
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          "gene_symbol": "ATP9B",
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          "transcript": "ENST00000899995.1",
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        {
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        },
        {
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          "consequences": [
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          ],
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          "exon_count": 26,
          "intron_rank": 25,
          "intron_rank_end": null,
          "gene_symbol": "ATP9B",
          "gene_hgnc_id": 13541,
          "hgvs_c": "c.3041-45A>G",
          "hgvs_p": null,
          "transcript": "ENST00000899992.1",
          "protein_id": "ENSP00000570051.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_length": 3177,
          "cdna_start": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000899992.1"
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
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      "gene_symbol": "ATP9B",
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      "gnomad_exomes_af": 0.873792,
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      "gnomad_genomes_homalt": 61057,
      "gnomad_mito_homoplasmic": null,
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      "computational_score_selected": -0.9399999976158142,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
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      "revel_prediction": null,
      "alphamissense_score": null,
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      "bayesdelnoaf_score": -0.94,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -1.07,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
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      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -12,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BA1",
      "acmg_by_gene": [
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "NM_198531.5",
          "gene_symbol": "ATP9B",
          "hgnc_id": 13541,
          "effects": [
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          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.3308-45A>G",
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      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}