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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: 3-4711790-A-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=4711790&ref=A&alt=C&genome=hg38&allGenes=true"API Response
json
{
  "variants": [
    {
      "chr": "3",
      "pos": 4711790,
      "ref": "A",
      "alt": "C",
      "effect": "missense_variant",
      "transcript": "ENST00000443694.5",
      "consequences": [
        {
          "aa_ref": "E",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 62,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.5025A>C",
          "hgvs_p": "p.Glu1675Asp",
          "transcript": "NM_001378452.1",
          "protein_id": "NP_001365381.1",
          "transcript_support_level": null,
          "aa_start": 1675,
          "aa_end": null,
          "aa_length": 2758,
          "cds_start": 5025,
          "cds_end": null,
          "cds_length": 8277,
          "cdna_start": 5375,
          "cdna_end": null,
          "cdna_length": 9908,
          "mane_select": "ENST00000649015.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "D",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 62,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.5025A>C",
          "hgvs_p": "p.Glu1675Asp",
          "transcript": "ENST00000649015.2",
          "protein_id": "ENSP00000497605.1",
          "transcript_support_level": null,
          "aa_start": 1675,
          "aa_end": null,
          "aa_length": 2758,
          "cds_start": 5025,
          "cds_end": null,
          "cds_length": 8277,
          "cdna_start": 5375,
          "cdna_end": null,
          "cdna_length": 9908,
          "mane_select": "NM_001378452.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "D",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 62,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.4998A>C",
          "hgvs_p": "p.Glu1666Asp",
          "transcript": "ENST00000354582.12",
          "protein_id": "ENSP00000346595.8",
          "transcript_support_level": 5,
          "aa_start": 1666,
          "aa_end": null,
          "aa_length": 2750,
          "cds_start": 4998,
          "cds_end": null,
          "cds_length": 8253,
          "cdna_start": 5348,
          "cdna_end": null,
          "cdna_length": 9876,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "D",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 62,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.4998A>C",
          "hgvs_p": "p.Glu1666Asp",
          "transcript": "ENST00000648266.1",
          "protein_id": "ENSP00000498014.1",
          "transcript_support_level": null,
          "aa_start": 1666,
          "aa_end": null,
          "aa_length": 2749,
          "cds_start": 4998,
          "cds_end": null,
          "cds_length": 8250,
          "cdna_start": 5242,
          "cdna_end": null,
          "cdna_length": 9767,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "D",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 38,
          "exon_rank_end": null,
          "exon_count": 61,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.4980A>C",
          "hgvs_p": "p.Glu1660Asp",
          "transcript": "ENST00000650294.1",
          "protein_id": "ENSP00000498056.1",
          "transcript_support_level": null,
          "aa_start": 1660,
          "aa_end": null,
          "aa_length": 2744,
          "cds_start": 4980,
          "cds_end": null,
          "cds_length": 8235,
          "cdna_start": 5117,
          "cdna_end": null,
          "cdna_length": 9353,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "D",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 38,
          "exon_rank_end": null,
          "exon_count": 61,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.4980A>C",
          "hgvs_p": "p.Glu1660Asp",
          "transcript": "ENST00000443694.5",
          "protein_id": "ENSP00000401671.2",
          "transcript_support_level": 1,
          "aa_start": 1660,
          "aa_end": null,
          "aa_length": 2743,
          "cds_start": 4980,
          "cds_end": null,
          "cds_length": 8232,
          "cdna_start": 5225,
          "cdna_end": null,
          "cdna_length": 9647,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "D",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 36,
          "exon_rank_end": null,
          "exon_count": 59,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.4953A>C",
          "hgvs_p": "p.Glu1651Asp",
          "transcript": "ENST00000648309.1",
          "protein_id": "ENSP00000497026.1",
          "transcript_support_level": null,
          "aa_start": 1651,
          "aa_end": null,
          "aa_length": 2734,
          "cds_start": 4953,
          "cds_end": null,
          "cds_length": 8205,
          "cdna_start": 4958,
          "cdna_end": null,
          "cdna_length": 9311,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "D",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 59,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.4998A>C",
          "hgvs_p": "p.Glu1666Asp",
          "transcript": "ENST00000357086.10",
          "protein_id": "ENSP00000349597.4",
          "transcript_support_level": 1,
          "aa_start": 1666,
          "aa_end": null,
          "aa_length": 2710,
          "cds_start": 4998,
          "cds_end": null,
          "cds_length": 8133,
          "cdna_start": 5351,
          "cdna_end": null,
          "cdna_length": 9767,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "D",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 38,
          "exon_rank_end": null,
          "exon_count": 58,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.4953A>C",
          "hgvs_p": "p.Glu1651Asp",
          "transcript": "ENST00000456211.8",
          "protein_id": "ENSP00000397885.2",
          "transcript_support_level": 1,
          "aa_start": 1651,
          "aa_end": null,
          "aa_length": 2695,
          "cds_start": 4953,
          "cds_end": null,
          "cds_length": 8088,
          "cdna_start": 5199,
          "cdna_end": null,
          "cdna_length": 9506,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "D",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.2835A>C",
          "hgvs_p": "p.Glu945Asp",
          "transcript": "ENST00000648038.1",
          "protein_id": "ENSP00000497872.1",
          "transcript_support_level": null,
          "aa_start": 945,
          "aa_end": null,
          "aa_length": 2012,
          "cds_start": 2835,
          "cds_end": null,
          "cds_length": 6039,
          "cdna_start": 2835,
          "cdna_end": null,
          "cdna_length": 6998,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "D",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
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          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.2325A>C",
          "hgvs_p": "p.Glu775Asp",
          "transcript": "ENST00000648431.1",
          "protein_id": "ENSP00000498149.1",
          "transcript_support_level": null,
          "aa_start": 775,
          "aa_end": null,
          "aa_length": 1817,
          "cds_start": 2325,
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          "cdna_start": 2327,
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          "cdna_length": 6517,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "D",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.1932A>C",
          "hgvs_p": "p.Glu644Asp",
          "transcript": "ENST00000648212.1",
          "protein_id": "ENSP00000498022.1",
          "transcript_support_level": null,
          "aa_start": 644,
          "aa_end": null,
          "aa_length": 1738,
          "cds_start": 1932,
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          "cds_length": 5217,
          "cdna_start": 1933,
          "cdna_end": null,
          "cdna_length": 6373,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 20,
          "intron_rank": 12,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.996+57904A>C",
          "hgvs_p": null,
          "transcript": "ENST00000544951.6",
          "protein_id": "ENSP00000440564.1",
          "transcript_support_level": 1,
          "aa_start": null,
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          "cds_start": -4,
          "cds_end": null,
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          "cdna_start": null,
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          "cdna_length": 2799,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 38,
          "exon_rank_end": null,
          "exon_count": 61,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.4980A>C",
          "hgvs_p": "p.Glu1660Asp",
          "transcript": "NM_001168272.2",
          "protein_id": "NP_001161744.1",
          "transcript_support_level": null,
          "aa_start": 1660,
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          "cds_start": 4980,
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          "cdna_start": 5330,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 59,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.4998A>C",
          "hgvs_p": "p.Glu1666Asp",
          "transcript": "NM_001099952.4",
          "protein_id": "NP_001093422.2",
          "transcript_support_level": null,
          "aa_start": 1666,
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          "cds_start": 4998,
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          "cds_length": 8133,
          "cdna_start": 5348,
          "cdna_end": null,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 38,
          "exon_rank_end": null,
          "exon_count": 58,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.4953A>C",
          "hgvs_p": "p.Glu1651Asp",
          "transcript": "NM_002222.7",
          "protein_id": "NP_002213.5",
          "transcript_support_level": null,
          "aa_start": 1651,
          "aa_end": null,
          "aa_length": 2695,
          "cds_start": 4953,
          "cds_end": null,
          "cds_length": 8088,
          "cdna_start": 5303,
          "cdna_end": null,
          "cdna_length": 9719,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 34,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.1356A>C",
          "hgvs_p": "p.Glu452Asp",
          "transcript": "ENST00000648016.1",
          "protein_id": "ENSP00000496893.1",
          "transcript_support_level": null,
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          "cds_length": 4644,
          "cdna_start": 1357,
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        },
        {
          "aa_ref": "E",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.600A>C",
          "hgvs_p": "p.Glu200Asp",
          "transcript": "ENST00000649414.1",
          "protein_id": "ENSP00000497099.1",
          "transcript_support_level": null,
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          "aa_end": null,
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          "cds_start": 600,
          "cds_end": null,
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          "cdna_start": 600,
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          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 3,
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          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.336A>C",
          "hgvs_p": "p.Glu112Asp",
          "transcript": "ENST00000648564.1",
          "protein_id": "ENSP00000497186.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 247,
          "cds_start": 336,
          "cds_end": null,
          "cds_length": 744,
          "cdna_start": 337,
          "cdna_end": null,
          "cdna_length": 745,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "D",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ITPR1",
          "gene_hgnc_id": 6180,
          "hgvs_c": "c.366A>C",
          "hgvs_p": "p.Glu122Asp",
          "transcript": "ENST00000648390.1",
          "protein_id": "ENSP00000497404.1",
          "transcript_support_level": null,
          "aa_start": 122,
          "aa_end": null,
          "aa_length": 176,
          "cds_start": 366,
          "cds_end": null,
          "cds_length": 531,
          "cdna_start": 368,
          "cdna_end": null,
          "cdna_length": 1601,
          "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": 38,
          "exon_rank_end": null,
          "exon_count": 61,
          "intron_rank": null,
          "intron_rank_end": null,
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        {
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        }
      ],
      "gene_symbol": "ITPR1",
      "gene_hgnc_id": 6180,
      "dbsnp": "rs1553706329",
      "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": 0.12703019380569458,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.215,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.7802,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.29,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.553,
      "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": -2,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Moderate,BP6_Moderate",
      "acmg_by_gene": [
        {
          "score": -2,
          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate",
            "BP6_Moderate"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000443694.5",
          "gene_symbol": "ITPR1",
          "hgnc_id": 6180,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.4980A>C",
          "hgvs_p": "p.Glu1660Asp"
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      ],
      "clinvar_disease": "Spinocerebellar ataxia type 29",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "Spinocerebellar ataxia type 29",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}