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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: 12-111598844-GCCGAGGACGAGGAGA-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=111598844&ref=GCCGAGGACGAGGAGA&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "12",
      "pos": 111598844,
      "ref": "GCCGAGGACGAGGAGA",
      "alt": "G",
      "effect": "disruptive_inframe_deletion",
      "transcript": "ENST00000673436.1",
      "consequences": [
        {
          "aa_ref": "VSSSSA",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "c.176_190delTCTCCTCGTCCTCGG",
          "hgvs_p": "p.Val59_Ser63del",
          "transcript": "NM_001372574.1",
          "protein_id": "NP_001359503.1",
          "transcript_support_level": null,
          "aa_start": 59,
          "aa_end": null,
          "aa_length": 1155,
          "cds_start": 176,
          "cds_end": null,
          "cds_length": 3468,
          "cdna_start": 471,
          "cdna_end": null,
          "cdna_length": 4347,
          "mane_select": "ENST00000673436.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "VSSSSA",
          "aa_alt": "A",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "c.176_190delTCTCCTCGTCCTCGG",
          "hgvs_p": "p.Val59_Ser63del",
          "transcript": "ENST00000673436.1",
          "protein_id": "ENSP00000500925.1",
          "transcript_support_level": null,
          "aa_start": 59,
          "aa_end": null,
          "aa_length": 1155,
          "cds_start": 176,
          "cds_end": null,
          "cds_length": 3468,
          "cdna_start": 471,
          "cdna_end": null,
          "cdna_length": 4347,
          "mane_select": "NM_001372574.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "VSSSSA",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "c.656_670delTCTCCTCGTCCTCGG",
          "hgvs_p": "p.Val219_Ser223del",
          "transcript": "ENST00000550104.5",
          "protein_id": "ENSP00000446576.2",
          "transcript_support_level": 1,
          "aa_start": 219,
          "aa_end": null,
          "aa_length": 1313,
          "cds_start": 656,
          "cds_end": null,
          "cds_length": 3942,
          "cdna_start": 832,
          "cdna_end": null,
          "cdna_length": 4648,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "VSSSSA",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "c.176_190delTCTCCTCGTCCTCGG",
          "hgvs_p": "p.Val59_Ser63del",
          "transcript": "ENST00000608853.5",
          "protein_id": "ENSP00000476504.1",
          "transcript_support_level": 1,
          "aa_start": 59,
          "aa_end": null,
          "aa_length": 1153,
          "cds_start": 176,
          "cds_end": null,
          "cds_length": 3462,
          "cdna_start": 506,
          "cdna_end": null,
          "cdna_length": 4376,
          "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": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "n.176_190delTCTCCTCGTCCTCGG",
          "hgvs_p": null,
          "transcript": "ENST00000483311.6",
          "protein_id": "ENSP00000446512.2",
          "transcript_support_level": 1,
          "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": 4159,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "c.-65+716_-65+730delTCTCCTCGTCCTCGG",
          "hgvs_p": null,
          "transcript": "ENST00000542287.6",
          "protein_id": "ENSP00000445583.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1073,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3222,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3443,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "c.-28+716_-28+730delTCTCCTCGTCCTCGG",
          "hgvs_p": null,
          "transcript": "ENST00000535949.5",
          "protein_id": "ENSP00000439338.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1006,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3021,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3205,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": null,
          "protein_coding": null,
          "strand": false,
          "consequences": [
            "bidirectional_gene_fusion"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "n.111598859_111598845delTCTCCTCGTCCTCGG",
          "hgvs_p": null,
          "transcript": null,
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "VSSSSA",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "c.176_190delTCTCCTCGTCCTCGG",
          "hgvs_p": "p.Val59_Ser63del",
          "transcript": "ENST00000673449.1",
          "protein_id": "ENSP00000500646.1",
          "transcript_support_level": null,
          "aa_start": 59,
          "aa_end": null,
          "aa_length": 1178,
          "cds_start": 176,
          "cds_end": null,
          "cds_length": 3537,
          "cdna_start": 278,
          "cdna_end": null,
          "cdna_length": 3754,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "VSSSSA",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "c.176_190delTCTCCTCGTCCTCGG",
          "hgvs_p": "p.Val59_Ser63del",
          "transcript": "ENST00000673557.1",
          "protein_id": "ENSP00000500766.1",
          "transcript_support_level": null,
          "aa_start": 59,
          "aa_end": null,
          "aa_length": 1167,
          "cds_start": 176,
          "cds_end": null,
          "cds_length": 3504,
          "cdna_start": 282,
          "cdna_end": null,
          "cdna_length": 3926,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "VSSSSA",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "c.176_190delTCTCCTCGTCCTCGG",
          "hgvs_p": "p.Val59_Ser63del",
          "transcript": "ENST00000643669.2",
          "protein_id": "ENSP00000494663.1",
          "transcript_support_level": null,
          "aa_start": 59,
          "aa_end": null,
          "aa_length": 1166,
          "cds_start": 176,
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          "cds_length": 3501,
          "cdna_start": 471,
          "cdna_end": null,
          "cdna_length": 4380,
          "mane_select": null,
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          "feature": null
        },
        {
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 1,
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          "exon_count": 25,
          "intron_rank": null,
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          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "c.176_190delTCTCCTCGTCCTCGG",
          "hgvs_p": "p.Val59_Ser63del",
          "transcript": "NM_002973.4",
          "protein_id": "NP_002964.4",
          "transcript_support_level": null,
          "aa_start": 59,
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          "aa_length": 1153,
          "cds_start": 176,
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          "cdna_start": 471,
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        },
        {
          "aa_ref": "VSSSSA",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 1,
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          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "c.176_190delTCTCCTCGTCCTCGG",
          "hgvs_p": "p.Val59_Ser63del",
          "transcript": "ENST00000672613.1",
          "protein_id": "ENSP00000500649.1",
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          "cds_start": 176,
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          "feature": null
        },
        {
          "aa_ref": "VSSSSA",
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 1,
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          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "c.176_190delTCTCCTCGTCCTCGG",
          "hgvs_p": "p.Val59_Ser63del",
          "transcript": "ENST00000389153.10",
          "protein_id": "ENSP00000373805.6",
          "transcript_support_level": 5,
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        },
        {
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          ],
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          "intron_rank": null,
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          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "c.176_190delTCTCCTCGTCCTCGG",
          "hgvs_p": "p.Val59_Ser63del",
          "transcript": "ENST00000673283.1",
          "protein_id": "ENSP00000500313.1",
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          "cdna_start": 235,
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          "feature": null
        },
        {
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          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "c.176_190delTCTCCTCGTCCTCGG",
          "hgvs_p": "p.Val59_Ser63del",
          "transcript": "ENST00000647305.1",
          "protein_id": "ENSP00000493897.1",
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        },
        {
          "aa_ref": "VSSSSA",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "c.176_190delTCTCCTCGTCCTCGG",
          "hgvs_p": "p.Val59_Ser63del",
          "transcript": "ENST00000644883.1",
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        },
        {
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          "protein_coding": false,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 1,
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          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "n.204_218delTCTCCTCGTCCTCGG",
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          "transcript": "ENST00000549455.1",
          "protein_id": null,
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        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
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          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "n.176_190delTCTCCTCGTCCTCGG",
          "hgvs_p": null,
          "transcript": "ENST00000642389.2",
          "protein_id": "ENSP00000496055.2",
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          "cdna_start": null,
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          "cdna_length": 4438,
          "mane_select": null,
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          "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": 1,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATXN2",
          "gene_hgnc_id": 10555,
          "hgvs_c": "n.14_28delTCTCCTCGTCCTCGG",
          "hgvs_p": null,
          "transcript": "ENST00000671792.1",
          "protein_id": "ENSP00000500090.1",
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          "aa_length": null,
          "cds_start": -4,
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        {
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          "gene_symbol": "ATXN2-AS",
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        },
        {
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          "consequences": [
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          "exon_count": 2,
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          "gene_symbol": "ATXN2-AS",
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          "transcript": "ENST00000726962.1",
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        }
      ],
      "gene_symbol": "ATXN2",
      "gene_hgnc_id": 10555,
      "dbsnp": "rs778119853",
      "frequency_reference_population": 0.00006790443,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 100,
      "gnomad_exomes_af": 0.0000703869,
      "gnomad_genomes_af": 0.0000462382,
      "gnomad_exomes_ac": 93,
      "gnomad_genomes_ac": 7,
      "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": 2.734,
      "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": -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": "ENST00000673436.1",
          "gene_symbol": "ATXN2",
          "hgnc_id": 10555,
          "effects": [
            "disruptive_inframe_deletion"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.176_190delTCTCCTCGTCCTCGG",
          "hgvs_p": "p.Val59_Ser63del"
        },
        {
          "score": -1,
          "benign_score": 1,
          "pathogenic_score": 0,
          "criteria": [
            "BP6"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000726950.1",
          "gene_symbol": "ATXN2-AS",
          "hgnc_id": 51838,
          "effects": [
            "non_coding_transcript_exon_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.3_17delGACCGAGGACGAGGA",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "GM3 synthase deficiency,not provided",
      "clinvar_classification": "Conflicting classifications of pathogenicity",
      "clinvar_review_status": "criteria provided, conflicting classifications",
      "clinvar_submissions_summary": "US:1 LB:1",
      "phenotype_combined": "GM3 synthase deficiency|not provided",
      "pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
      "custom_annotations": null
    }
  ],
  "message": null
}