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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: X-71141265-G-GCAGCAA (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=71141265&ref=G&alt=GCAGCAA&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "X",
      "pos": 71141265,
      "ref": "G",
      "alt": "GCAGCAA",
      "effect": "disruptive_inframe_insertion",
      "transcript": "ENST00000374080.8",
      "consequences": [
        {
          "aa_ref": "Q",
          "aa_alt": "QQQ",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_insertion"
          ],
          "exon_rank": 43,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.6315_6320dupACAGCA",
          "hgvs_p": "p.Gln2106_Gln2107dup",
          "transcript": "NM_005120.3",
          "protein_id": "NP_005111.2",
          "transcript_support_level": null,
          "aa_start": 2107,
          "aa_end": null,
          "aa_length": 2177,
          "cds_start": 6321,
          "cds_end": null,
          "cds_length": 6534,
          "cdna_start": 6480,
          "cdna_end": null,
          "cdna_length": 6925,
          "mane_select": "ENST00000374080.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "QQQ",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_insertion"
          ],
          "exon_rank": 43,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.6315_6320dupACAGCA",
          "hgvs_p": "p.Gln2106_Gln2107dup",
          "transcript": "ENST00000374080.8",
          "protein_id": "ENSP00000363193.3",
          "transcript_support_level": 1,
          "aa_start": 2107,
          "aa_end": null,
          "aa_length": 2177,
          "cds_start": 6321,
          "cds_end": null,
          "cds_length": 6534,
          "cdna_start": 6480,
          "cdna_end": null,
          "cdna_length": 6925,
          "mane_select": "NM_005120.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "QQQ",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_insertion"
          ],
          "exon_rank": 43,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.6324_6329dupACAGCA",
          "hgvs_p": "p.Gln2109_Gln2110dup",
          "transcript": "ENST00000374102.6",
          "protein_id": "ENSP00000363215.2",
          "transcript_support_level": 1,
          "aa_start": 2110,
          "aa_end": null,
          "aa_length": 2180,
          "cds_start": 6330,
          "cds_end": null,
          "cds_length": 6543,
          "cdna_start": 6456,
          "cdna_end": null,
          "cdna_length": 6901,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "QQQ",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_insertion"
          ],
          "exon_rank": 43,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.6321_6326dupACAGCA",
          "hgvs_p": "p.Gln2108_Gln2109dup",
          "transcript": "ENST00000690145.1",
          "protein_id": "ENSP00000508818.1",
          "transcript_support_level": null,
          "aa_start": 2109,
          "aa_end": null,
          "aa_length": 2179,
          "cds_start": 6327,
          "cds_end": null,
          "cds_length": 6540,
          "cdna_start": 6357,
          "cdna_end": null,
          "cdna_length": 6739,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "QQQ",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_insertion"
          ],
          "exon_rank": 43,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.6312_6317dupACAGCA",
          "hgvs_p": "p.Gln2105_Gln2106dup",
          "transcript": "ENST00000692304.1",
          "protein_id": "ENSP00000508427.1",
          "transcript_support_level": null,
          "aa_start": 2106,
          "aa_end": null,
          "aa_length": 2176,
          "cds_start": 6318,
          "cds_end": null,
          "cds_length": 6531,
          "cdna_start": 6530,
          "cdna_end": null,
          "cdna_length": 8628,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "QQQ",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_insertion"
          ],
          "exon_rank": 44,
          "exon_rank_end": null,
          "exon_count": 46,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.6249_6254dupACAGCA",
          "hgvs_p": "p.Gln2084_Gln2085dup",
          "transcript": "ENST00000690242.1",
          "protein_id": "ENSP00000510090.1",
          "transcript_support_level": null,
          "aa_start": 2085,
          "aa_end": null,
          "aa_length": 2155,
          "cds_start": 6255,
          "cds_end": null,
          "cds_length": 6468,
          "cdna_start": 6467,
          "cdna_end": null,
          "cdna_length": 6912,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "QQQ",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_insertion"
          ],
          "exon_rank": 44,
          "exon_rank_end": null,
          "exon_count": 46,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.6240_6245dupACAGCA",
          "hgvs_p": "p.Gln2081_Gln2082dup",
          "transcript": "ENST00000687382.1",
          "protein_id": "ENSP00000510724.1",
          "transcript_support_level": null,
          "aa_start": 2082,
          "aa_end": null,
          "aa_length": 2152,
          "cds_start": 6246,
          "cds_end": null,
          "cds_length": 6459,
          "cdna_start": 6445,
          "cdna_end": null,
          "cdna_length": 6764,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "QQQ",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_insertion"
          ],
          "exon_rank": 43,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.6195_6200dupACAGCA",
          "hgvs_p": "p.Gln2066_Gln2067dup",
          "transcript": "ENST00000333646.11",
          "protein_id": "ENSP00000333125.8",
          "transcript_support_level": 5,
          "aa_start": 2067,
          "aa_end": null,
          "aa_length": 2137,
          "cds_start": 6201,
          "cds_end": null,
          "cds_length": 6414,
          "cdna_start": 6360,
          "cdna_end": null,
          "cdna_length": 6797,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "QQQ",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_insertion"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 31,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.4266_4271dupACAGCA",
          "hgvs_p": "p.Gln1423_Gln1424dup",
          "transcript": "ENST00000693391.1",
          "protein_id": "ENSP00000509563.1",
          "transcript_support_level": null,
          "aa_start": 1424,
          "aa_end": null,
          "aa_length": 1494,
          "cds_start": 4272,
          "cds_end": null,
          "cds_length": 4485,
          "cdna_start": 4272,
          "cdna_end": null,
          "cdna_length": 4699,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "QQQ",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_insertion"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.1287_1292dupACAGCA",
          "hgvs_p": "p.Gln430_Gln431dup",
          "transcript": "ENST00000444034.2",
          "protein_id": "ENSP00000404373.2",
          "transcript_support_level": 5,
          "aa_start": 431,
          "aa_end": null,
          "aa_length": 501,
          "cds_start": 1293,
          "cds_end": null,
          "cds_length": 1506,
          "cdna_start": 1293,
          "cdna_end": null,
          "cdna_length": 1675,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "QQQ",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_insertion"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "c.357_362dupACAGCA",
          "hgvs_p": "p.Gln120_Gln121dup",
          "transcript": "ENST00000688231.1",
          "protein_id": "ENSP00000508591.1",
          "transcript_support_level": null,
          "aa_start": 121,
          "aa_end": null,
          "aa_length": 246,
          "cds_start": 363,
          "cds_end": null,
          "cds_length": 741,
          "cdna_start": 365,
          "cdna_end": null,
          "cdna_length": 854,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.3013_3018dupACAGCA",
          "hgvs_p": null,
          "transcript": "ENST00000685182.1",
          "protein_id": null,
          "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": 3446,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.2701_2706dupACAGCA",
          "hgvs_p": null,
          "transcript": "ENST00000686169.1",
          "protein_id": null,
          "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": 3148,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 43,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.*6220_*6225dupACAGCA",
          "hgvs_p": null,
          "transcript": "ENST00000686548.1",
          "protein_id": "ENSP00000509582.1",
          "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": 6852,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.3030_3035dupACAGCA",
          "hgvs_p": null,
          "transcript": "ENST00000687161.1",
          "protein_id": null,
          "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": 3481,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.3074_3079dupACAGCA",
          "hgvs_p": null,
          "transcript": "ENST00000687701.1",
          "protein_id": null,
          "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": 3499,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.988_993dupACAGCA",
          "hgvs_p": null,
          "transcript": "ENST00000687973.1",
          "protein_id": null,
          "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": 1423,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 25,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.4310_4315dupACAGCA",
          "hgvs_p": null,
          "transcript": "ENST00000688079.1",
          "protein_id": null,
          "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": 4676,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.1875_1880dupACAGCA",
          "hgvs_p": null,
          "transcript": "ENST00000688508.1",
          "protein_id": null,
          "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": 2263,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MED12",
          "gene_hgnc_id": 11957,
          "hgvs_c": "n.*166_*171dupACAGCA",
          "hgvs_p": null,
          "transcript": "ENST00000688774.1",
          "protein_id": "ENSP00000508823.1",
          "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": 1186,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
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          "cdna_end": null,
          "cdna_length": 1015,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "MED12",
      "gene_hgnc_id": 11957,
      "dbsnp": "rs764789036",
      "frequency_reference_population": 0.000101037935,
      "hom_count_reference_population": 2,
      "allele_count_reference_population": 11,
      "gnomad_exomes_af": 0.0000180882,
      "gnomad_genomes_af": 0.000101038,
      "gnomad_exomes_ac": 19,
      "gnomad_genomes_ac": 11,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": null,
      "computational_prediction_selected": null,
      "computational_source_selected": null,
      "splice_score_selected": null,
      "splice_prediction_selected": null,
      "splice_source_selected": null,
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": null,
      "bayesdelnoaf_prediction": null,
      "phylop100way_score": 2.202,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": null,
      "spliceai_max_prediction": null,
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -10,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP3,BP6,BS1,BS2",
      "acmg_by_gene": [
        {
          "score": -10,
          "benign_score": 10,
          "pathogenic_score": 0,
          "criteria": [
            "BP3",
            "BP6",
            "BS1",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000374080.8",
          "gene_symbol": "MED12",
          "hgnc_id": 11957,
          "effects": [
            "disruptive_inframe_insertion"
          ],
          "inheritance_mode": "XL",
          "hgvs_c": "c.6315_6320dupACAGCA",
          "hgvs_p": "p.Gln2106_Gln2107dup"
        },
        {
          "score": -5,
          "benign_score": 5,
          "pathogenic_score": 0,
          "criteria": [
            "BP6",
            "BS2"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000740246.1",
          "gene_symbol": "ENSG00000228427",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.347-420_347-415dupTTGCTG",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "FG syndrome,Familial thoracic aortic aneurysm and aortic dissection,not provided",
      "clinvar_classification": "Conflicting classifications of pathogenicity",
      "clinvar_review_status": "criteria provided, conflicting classifications",
      "clinvar_submissions_summary": "US:1 LB:2",
      "phenotype_combined": "not provided|Familial thoracic aortic aneurysm and aortic dissection|FG syndrome",
      "pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
      "custom_annotations": null
    }
  ],
  "message": null
}