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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: 9-83859200-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=83859200&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "9",
      "pos": 83859200,
      "ref": "T",
      "alt": "C",
      "effect": "missense_variant",
      "transcript": "ENST00000297814.7",
      "consequences": [
        {
          "aa_ref": "N",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIF27",
          "gene_hgnc_id": 18632,
          "hgvs_c": "c.3106A>G",
          "hgvs_p": "p.Asn1036Asp",
          "transcript": "NM_017576.4",
          "protein_id": "NP_060046.1",
          "transcript_support_level": null,
          "aa_start": 1036,
          "aa_end": null,
          "aa_length": 1401,
          "cds_start": 3106,
          "cds_end": null,
          "cds_length": 4206,
          "cdna_start": 3255,
          "cdna_end": null,
          "cdna_length": 7257,
          "mane_select": "ENST00000297814.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "D",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIF27",
          "gene_hgnc_id": 18632,
          "hgvs_c": "c.3106A>G",
          "hgvs_p": "p.Asn1036Asp",
          "transcript": "ENST00000297814.7",
          "protein_id": "ENSP00000297814.2",
          "transcript_support_level": 1,
          "aa_start": 1036,
          "aa_end": null,
          "aa_length": 1401,
          "cds_start": 3106,
          "cds_end": null,
          "cds_length": 4206,
          "cdna_start": 3255,
          "cdna_end": null,
          "cdna_length": 7257,
          "mane_select": "NM_017576.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIF27",
          "gene_hgnc_id": 18632,
          "hgvs_c": "c.2908A>G",
          "hgvs_p": "p.Asn970Asp",
          "transcript": "ENST00000413982.5",
          "protein_id": "ENSP00000401688.1",
          "transcript_support_level": 1,
          "aa_start": 970,
          "aa_end": null,
          "aa_length": 1335,
          "cds_start": 2908,
          "cds_end": null,
          "cds_length": 4008,
          "cdna_start": 3090,
          "cdna_end": null,
          "cdna_length": 4493,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIF27",
          "gene_hgnc_id": 18632,
          "hgvs_c": "c.2815A>G",
          "hgvs_p": "p.Asn939Asp",
          "transcript": "ENST00000334204.6",
          "protein_id": "ENSP00000333928.2",
          "transcript_support_level": 1,
          "aa_start": 939,
          "aa_end": null,
          "aa_length": 1304,
          "cds_start": 2815,
          "cds_end": null,
          "cds_length": 3915,
          "cdna_start": 2997,
          "cdna_end": null,
          "cdna_length": 4400,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIF27",
          "gene_hgnc_id": 18632,
          "hgvs_c": "c.2908A>G",
          "hgvs_p": "p.Asn970Asp",
          "transcript": "NM_001271927.3",
          "protein_id": "NP_001258856.1",
          "transcript_support_level": null,
          "aa_start": 970,
          "aa_end": null,
          "aa_length": 1335,
          "cds_start": 2908,
          "cds_end": null,
          "cds_length": 4008,
          "cdna_start": 3057,
          "cdna_end": null,
          "cdna_length": 7059,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIF27",
          "gene_hgnc_id": 18632,
          "hgvs_c": "c.2815A>G",
          "hgvs_p": "p.Asn939Asp",
          "transcript": "NM_001271928.3",
          "protein_id": "NP_001258857.1",
          "transcript_support_level": null,
          "aa_start": 939,
          "aa_end": null,
          "aa_length": 1304,
          "cds_start": 2815,
          "cds_end": null,
          "cds_length": 3915,
          "cdna_start": 2964,
          "cdna_end": null,
          "cdna_length": 6966,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIF27",
          "gene_hgnc_id": 18632,
          "hgvs_c": "c.1666A>G",
          "hgvs_p": "p.Asn556Asp",
          "transcript": "NM_001354070.2",
          "protein_id": "NP_001340999.1",
          "transcript_support_level": null,
          "aa_start": 556,
          "aa_end": null,
          "aa_length": 921,
          "cds_start": 1666,
          "cds_end": null,
          "cds_length": 2766,
          "cdna_start": 2488,
          "cdna_end": null,
          "cdna_length": 6490,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIF27",
          "gene_hgnc_id": 18632,
          "hgvs_c": "c.3184A>G",
          "hgvs_p": "p.Asn1062Asp",
          "transcript": "XM_011518848.4",
          "protein_id": "XP_011517150.1",
          "transcript_support_level": null,
          "aa_start": 1062,
          "aa_end": null,
          "aa_length": 1427,
          "cds_start": 3184,
          "cds_end": null,
          "cds_length": 4284,
          "cdna_start": 3333,
          "cdna_end": null,
          "cdna_length": 7335,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "N",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIF27",
          "gene_hgnc_id": 18632,
          "hgvs_c": "c.3184A>G",
          "hgvs_p": "p.Asn1062Asp",
          "transcript": "XM_011518849.3",
          "protein_id": "XP_011517151.1",
          "transcript_support_level": null,
          "aa_start": 1062,
          "aa_end": null,
          "aa_length": 1427,
          "cds_start": 3184,
          "cds_end": null,
          "cds_length": 4284,
          "cdna_start": 3440,
          "cdna_end": null,
          "cdna_length": 7442,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "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": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIF27",
          "gene_hgnc_id": 18632,
          "hgvs_c": "c.3184A>G",
          "hgvs_p": "p.Asn1062Asp",
          "transcript": "XM_011518850.3",
          "protein_id": "XP_011517152.1",
          "transcript_support_level": null,
          "aa_start": 1062,
          "aa_end": null,
          "aa_length": 1427,
          "cds_start": 3184,
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          "cdna_start": 3717,
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          "cdna_length": 7719,
          "mane_select": null,
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        },
        {
          "aa_ref": "N",
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          "strand": false,
          "consequences": [
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          ],
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          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "KIF27",
          "gene_hgnc_id": 18632,
          "hgvs_c": "c.3184A>G",
          "hgvs_p": "p.Asn1062Asp",
          "transcript": "XM_017014900.2",
          "protein_id": "XP_016870389.1",
          "transcript_support_level": null,
          "aa_start": 1062,
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          "aa_length": 1427,
          "cds_start": 3184,
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          "mane_select": null,
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          "feature": null
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        {
          "aa_ref": "N",
          "aa_alt": "D",
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          "consequences": [
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          ],
          "exon_rank": 17,
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          "exon_count": 21,
          "intron_rank": null,
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          "gene_symbol": "KIF27",
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        {
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          "intron_rank": null,
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          "gene_symbol": "KIF27",
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          "hgvs_c": "c.3184A>G",
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        {
          "aa_ref": "N",
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          "intron_rank": null,
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          "gene_symbol": "KIF27",
          "gene_hgnc_id": 18632,
          "hgvs_c": "c.3184A>G",
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          "transcript": "XM_047423570.1",
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        {
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        {
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          "intron_rank": null,
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          "gene_symbol": "KIF27",
          "gene_hgnc_id": 18632,
          "hgvs_c": "c.3106A>G",
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          "transcript": "XM_017014903.2",
          "protein_id": "XP_016870392.1",
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        {
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          "intron_rank": null,
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          "hgvs_c": "c.3106A>G",
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          "transcript": "XM_017014904.2",
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        {
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        {
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        {
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          "consequences": [
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          ],
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          "exon_count": 19,
          "intron_rank": null,
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          "gene_symbol": "KIF27",
          "gene_hgnc_id": 18632,
          "hgvs_c": "c.3106A>G",
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          "transcript": "XM_047423574.1",
          "protein_id": "XP_047279530.1",
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        },
        {
          "aa_ref": "N",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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      "computational_score_selected": 0.0038152337074279785,
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      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.176,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.0728,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.59,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 2.058,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
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      "apogee2_score": null,
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      "acmg_score": -20,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BA1",
      "acmg_by_gene": [
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            "BP6_Very_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000297814.7",
          "gene_symbol": "KIF27",
          "hgnc_id": 18632,
          "effects": [
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          "hgvs_p": "p.Asn1036Asp"
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        {
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          "pathogenic_score": 0,
          "criteria": [
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            "BP6_Very_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000589817.1",
          "gene_symbol": "ENSG00000226877",
          "hgnc_id": null,
          "effects": [
            "non_coding_transcript_exon_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.603T>C",
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        },
        {
          "score": -20,
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          "pathogenic_score": 0,
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            "BP6_Very_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "XR_007061620.1",
          "gene_symbol": "LOC124900638",
          "hgnc_id": null,
          "effects": [
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          ],
          "inheritance_mode": "",
          "hgvs_c": "n.*40T>C",
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      ],
      "clinvar_disease": "not provided,not specified",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "B:2",
      "phenotype_combined": "not specified|not provided",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}