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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: 2-127259306-C-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=127259306&ref=C&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 127259306,
      "ref": "C",
      "alt": "G",
      "effect": "missense_variant",
      "transcript": "ENST00000285398.7",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "c.2207G>C",
          "hgvs_p": "p.Arg736Thr",
          "transcript": "NM_000122.2",
          "protein_id": "NP_000113.1",
          "transcript_support_level": null,
          "aa_start": 736,
          "aa_end": null,
          "aa_length": 782,
          "cds_start": 2207,
          "cds_end": null,
          "cds_length": 2349,
          "cdna_start": 2270,
          "cdna_end": null,
          "cdna_length": 2718,
          "mane_select": "ENST00000285398.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "T",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "c.2207G>C",
          "hgvs_p": "p.Arg736Thr",
          "transcript": "ENST00000285398.7",
          "protein_id": "ENSP00000285398.2",
          "transcript_support_level": 1,
          "aa_start": 736,
          "aa_end": null,
          "aa_length": 782,
          "cds_start": 2207,
          "cds_end": null,
          "cds_length": 2349,
          "cdna_start": 2270,
          "cdna_end": null,
          "cdna_length": 2718,
          "mane_select": "NM_000122.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "c.2282G>C",
          "hgvs_p": "p.Arg761Thr",
          "transcript": "ENST00000647169.1",
          "protein_id": "ENSP00000495619.1",
          "transcript_support_level": null,
          "aa_start": 761,
          "aa_end": null,
          "aa_length": 807,
          "cds_start": 2282,
          "cds_end": null,
          "cds_length": 2424,
          "cdna_start": 2345,
          "cdna_end": null,
          "cdna_length": 2787,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "c.2015G>C",
          "hgvs_p": "p.Arg672Thr",
          "transcript": "NM_001303416.2",
          "protein_id": "NP_001290345.1",
          "transcript_support_level": null,
          "aa_start": 672,
          "aa_end": null,
          "aa_length": 718,
          "cds_start": 2015,
          "cds_end": null,
          "cds_length": 2157,
          "cdna_start": 2467,
          "cdna_end": null,
          "cdna_length": 2915,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "c.2015G>C",
          "hgvs_p": "p.Arg672Thr",
          "transcript": "NM_001303418.2",
          "protein_id": "NP_001290347.1",
          "transcript_support_level": null,
          "aa_start": 672,
          "aa_end": null,
          "aa_length": 718,
          "cds_start": 2015,
          "cds_end": null,
          "cds_length": 2157,
          "cdna_start": 2529,
          "cdna_end": null,
          "cdna_length": 2977,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "c.2225G>C",
          "hgvs_p": "p.Arg742Thr",
          "transcript": "XM_011510794.3",
          "protein_id": "XP_011509096.1",
          "transcript_support_level": null,
          "aa_start": 742,
          "aa_end": null,
          "aa_length": 788,
          "cds_start": 2225,
          "cds_end": null,
          "cds_length": 2367,
          "cdna_start": 2288,
          "cdna_end": null,
          "cdna_length": 2736,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "c.1769G>C",
          "hgvs_p": "p.Arg590Thr",
          "transcript": "XM_011510795.2",
          "protein_id": "XP_011509097.1",
          "transcript_support_level": null,
          "aa_start": 590,
          "aa_end": null,
          "aa_length": 636,
          "cds_start": 1769,
          "cds_end": null,
          "cds_length": 1911,
          "cdna_start": 2055,
          "cdna_end": null,
          "cdna_length": 2503,
          "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": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "n.*2188G>C",
          "hgvs_p": null,
          "transcript": "ENST00000426778.5",
          "protein_id": "ENSP00000415335.1",
          "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": 2916,
          "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": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "n.*2250G>C",
          "hgvs_p": null,
          "transcript": "ENST00000445889.5",
          "protein_id": "ENSP00000390888.1",
          "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": 2920,
          "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": 1,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "n.3577G>C",
          "hgvs_p": null,
          "transcript": "ENST00000491292.5",
          "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": 4018,
          "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": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "n.*1696G>C",
          "hgvs_p": null,
          "transcript": "ENST00000644317.1",
          "protein_id": "ENSP00000494012.1",
          "transcript_support_level": null,
          "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": 2345,
          "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": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "n.*2419G>C",
          "hgvs_p": null,
          "transcript": "ENST00000645233.1",
          "protein_id": "ENSP00000494116.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 3398,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "n.*979G>C",
          "hgvs_p": null,
          "transcript": "ENST00000645467.1",
          "protein_id": "ENSP00000494889.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2807,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "n.*657G>C",
          "hgvs_p": null,
          "transcript": "ENST00000645736.1",
          "protein_id": "ENSP00000494545.1",
          "transcript_support_level": null,
          "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": 2297,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "n.2942G>C",
          "hgvs_p": null,
          "transcript": "ENST00000646042.1",
          "protein_id": null,
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          "cdna_start": null,
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          "cdna_length": 3390,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "n.*1674G>C",
          "hgvs_p": null,
          "transcript": "ENST00000646654.1",
          "protein_id": "ENSP00000494526.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 2656,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "n.*2188G>C",
          "hgvs_p": null,
          "transcript": "ENST00000426778.5",
          "protein_id": "ENSP00000415335.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 2916,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "n.*2250G>C",
          "hgvs_p": null,
          "transcript": "ENST00000445889.5",
          "protein_id": "ENSP00000390888.1",
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          "aa_start": null,
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          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "n.*1696G>C",
          "hgvs_p": null,
          "transcript": "ENST00000644317.1",
          "protein_id": "ENSP00000494012.1",
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "n.*2419G>C",
          "hgvs_p": null,
          "transcript": "ENST00000645233.1",
          "protein_id": "ENSP00000494116.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3398,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC3",
          "gene_hgnc_id": 3435,
          "hgvs_c": "n.*979G>C",
          "hgvs_p": null,
          "transcript": "ENST00000645467.1",
          "protein_id": "ENSP00000494889.1",
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        },
        {
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        },
        {
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          "hgvs_c": "n.*1674G>C",
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          "transcript": "ENST00000646654.1",
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        },
        {
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          "exon_count": 5,
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          "gene_symbol": "ERCC3",
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          "hgvs_c": "c.394-1704G>C",
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          "transcript": "ENST00000647496.1",
          "protein_id": "ENSP00000496038.1",
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      ],
      "gene_symbol": "ERCC3",
      "gene_hgnc_id": 3435,
      "dbsnp": "rs587778276",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.08604574203491211,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.076,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.2102,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.48,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.235,
      "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": 0,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2,BP4_Moderate",
      "acmg_by_gene": [
        {
          "score": 0,
          "benign_score": 2,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000285398.7",
          "gene_symbol": "ERCC3",
          "hgnc_id": 3435,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AR,AD",
          "hgvs_c": "c.2207G>C",
          "hgvs_p": "p.Arg736Thr"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}