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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-71141247-ACAG-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=71141247&ref=ACAG&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "X",
      "pos": 71141247,
      "ref": "ACAG",
      "alt": "A",
      "effect": "disruptive_inframe_deletion",
      "transcript": "ENST00000374080.8",
      "consequences": [
        {
          "aa_ref": "QQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "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.6306_6308delGCA",
          "hgvs_p": "p.Gln2103del",
          "transcript": "NM_005120.3",
          "protein_id": "NP_005111.2",
          "transcript_support_level": null,
          "aa_start": 2102,
          "aa_end": null,
          "aa_length": 2177,
          "cds_start": 6306,
          "cds_end": null,
          "cds_length": 6534,
          "cdna_start": 6465,
          "cdna_end": null,
          "cdna_length": 6925,
          "mane_select": "ENST00000374080.8",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQ",
          "aa_alt": "Q",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "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.6306_6308delGCA",
          "hgvs_p": "p.Gln2103del",
          "transcript": "ENST00000374080.8",
          "protein_id": "ENSP00000363193.3",
          "transcript_support_level": 1,
          "aa_start": 2102,
          "aa_end": null,
          "aa_length": 2177,
          "cds_start": 6306,
          "cds_end": null,
          "cds_length": 6534,
          "cdna_start": 6465,
          "cdna_end": null,
          "cdna_length": 6925,
          "mane_select": "NM_005120.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "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_6317delGCA",
          "hgvs_p": "p.Gln2106del",
          "transcript": "ENST00000374102.6",
          "protein_id": "ENSP00000363215.2",
          "transcript_support_level": 1,
          "aa_start": 2105,
          "aa_end": null,
          "aa_length": 2180,
          "cds_start": 6315,
          "cds_end": null,
          "cds_length": 6543,
          "cdna_start": 6441,
          "cdna_end": null,
          "cdna_length": 6901,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "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_6314delGCA",
          "hgvs_p": "p.Gln2105del",
          "transcript": "ENST00000690145.1",
          "protein_id": "ENSP00000508818.1",
          "transcript_support_level": null,
          "aa_start": 2104,
          "aa_end": null,
          "aa_length": 2179,
          "cds_start": 6312,
          "cds_end": null,
          "cds_length": 6540,
          "cdna_start": 6342,
          "cdna_end": null,
          "cdna_length": 6739,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "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.6303_6305delGCA",
          "hgvs_p": "p.Gln2102del",
          "transcript": "ENST00000692304.1",
          "protein_id": "ENSP00000508427.1",
          "transcript_support_level": null,
          "aa_start": 2101,
          "aa_end": null,
          "aa_length": 2176,
          "cds_start": 6303,
          "cds_end": null,
          "cds_length": 6531,
          "cdna_start": 6515,
          "cdna_end": null,
          "cdna_length": 8628,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "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_6242delGCA",
          "hgvs_p": "p.Gln2081del",
          "transcript": "ENST00000690242.1",
          "protein_id": "ENSP00000510090.1",
          "transcript_support_level": null,
          "aa_start": 2080,
          "aa_end": null,
          "aa_length": 2155,
          "cds_start": 6240,
          "cds_end": null,
          "cds_length": 6468,
          "cdna_start": 6452,
          "cdna_end": null,
          "cdna_length": 6912,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "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.6231_6233delGCA",
          "hgvs_p": "p.Gln2078del",
          "transcript": "ENST00000687382.1",
          "protein_id": "ENSP00000510724.1",
          "transcript_support_level": null,
          "aa_start": 2077,
          "aa_end": null,
          "aa_length": 2152,
          "cds_start": 6231,
          "cds_end": null,
          "cds_length": 6459,
          "cdna_start": 6430,
          "cdna_end": null,
          "cdna_length": 6764,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "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.6186_6188delGCA",
          "hgvs_p": "p.Gln2063del",
          "transcript": "ENST00000333646.11",
          "protein_id": "ENSP00000333125.8",
          "transcript_support_level": 5,
          "aa_start": 2062,
          "aa_end": null,
          "aa_length": 2137,
          "cds_start": 6186,
          "cds_end": null,
          "cds_length": 6414,
          "cdna_start": 6345,
          "cdna_end": null,
          "cdna_length": 6797,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "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.4257_4259delGCA",
          "hgvs_p": "p.Gln1420del",
          "transcript": "ENST00000693391.1",
          "protein_id": "ENSP00000509563.1",
          "transcript_support_level": null,
          "aa_start": 1419,
          "aa_end": null,
          "aa_length": 1494,
          "cds_start": 4257,
          "cds_end": null,
          "cds_length": 4485,
          "cdna_start": 4257,
          "cdna_end": null,
          "cdna_length": 4699,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "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.1278_1280delGCA",
          "hgvs_p": "p.Gln427del",
          "transcript": "ENST00000444034.2",
          "protein_id": "ENSP00000404373.2",
          "transcript_support_level": 5,
          "aa_start": 426,
          "aa_end": null,
          "aa_length": 501,
          "cds_start": 1278,
          "cds_end": null,
          "cds_length": 1506,
          "cdna_start": 1278,
          "cdna_end": null,
          "cdna_length": 1675,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "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.348_350delGCA",
          "hgvs_p": "p.Gln117del",
          "transcript": "ENST00000688231.1",
          "protein_id": "ENSP00000508591.1",
          "transcript_support_level": null,
          "aa_start": 116,
          "aa_end": null,
          "aa_length": 246,
          "cds_start": 348,
          "cds_end": null,
          "cds_length": 741,
          "cdna_start": 350,
          "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.3004_3006delGCA",
          "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.2692_2694delGCA",
          "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.*6211_*6213delGCA",
          "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.3021_3023delGCA",
          "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.3065_3067delGCA",
          "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.979_981delGCA",
          "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.4301_4303delGCA",
          "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.1866_1868delGCA",
          "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.*157_*159delGCA",
          "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,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
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      "dbsnp": "rs766775649",
      "frequency_reference_population": 0.00011680766,
      "hom_count_reference_population": 4,
      "allele_count_reference_population": 134,
      "gnomad_exomes_af": 0.000127281,
      "gnomad_genomes_af": 0.0000181638,
      "gnomad_exomes_ac": 132,
      "gnomad_genomes_ac": 2,
      "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": 0.009999999776482582,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": null,
      "bayesdelnoaf_prediction": null,
      "phylop100way_score": 3.821,
      "phylop100way_prediction": "Uncertain_significance",
      "spliceai_max_score": 0.01,
      "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": -6,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "BP3,BP6,BS2",
      "acmg_by_gene": [
        {
          "score": -6,
          "benign_score": 6,
          "pathogenic_score": 0,
          "criteria": [
            "BP3",
            "BP6",
            "BS2"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000374080.8",
          "gene_symbol": "MED12",
          "hgnc_id": 11957,
          "effects": [
            "disruptive_inframe_deletion"
          ],
          "inheritance_mode": "XL",
          "hgvs_c": "c.6306_6308delGCA",
          "hgvs_p": "p.Gln2103del"
        },
        {
          "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.347-399_347-397delCTG",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "FG syndrome,Familial thoracic aortic aneurysm and aortic dissection,MED12-related disorder,not provided",
      "clinvar_classification": "Conflicting classifications of pathogenicity",
      "clinvar_review_status": "criteria provided, conflicting classifications",
      "clinvar_submissions_summary": "US:2 LB:1",
      "phenotype_combined": "MED12-related disorder|FG syndrome|not provided|Familial thoracic aortic aneurysm and aortic dissection",
      "pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
      "custom_annotations": null
    }
  ],
  "message": null
}