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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: 10-72368348-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=72368348&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "10",
      "pos": 72368348,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "NM_001195518.2",
      "consequences": [
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "c.1278C>T",
          "hgvs_p": "p.Gly426Gly",
          "transcript": "NM_001195518.2",
          "protein_id": "NP_001182447.1",
          "transcript_support_level": null,
          "aa_start": 426,
          "aa_end": null,
          "aa_length": 476,
          "cds_start": 1278,
          "cds_end": null,
          "cds_length": 1431,
          "cdna_start": 1349,
          "cdna_end": null,
          "cdna_length": 2357,
          "mane_select": "ENST00000361114.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "c.1278C>T",
          "hgvs_p": "p.Gly426Gly",
          "transcript": "ENST00000361114.10",
          "protein_id": "ENSP00000354415.5",
          "transcript_support_level": 1,
          "aa_start": 426,
          "aa_end": null,
          "aa_length": 476,
          "cds_start": 1278,
          "cds_end": null,
          "cds_length": 1431,
          "cdna_start": 1349,
          "cdna_end": null,
          "cdna_length": 2357,
          "mane_select": "NM_001195518.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "c.1509C>T",
          "hgvs_p": "p.Gly503Gly",
          "transcript": "NM_001441218.1",
          "protein_id": "NP_001428147.1",
          "transcript_support_level": null,
          "aa_start": 503,
          "aa_end": null,
          "aa_length": 553,
          "cds_start": 1509,
          "cds_end": null,
          "cds_length": 1662,
          "cdna_start": 1580,
          "cdna_end": null,
          "cdna_length": 2588,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "c.1446C>T",
          "hgvs_p": "p.Gly482Gly",
          "transcript": "NM_001441219.1",
          "protein_id": "NP_001428148.1",
          "transcript_support_level": null,
          "aa_start": 482,
          "aa_end": null,
          "aa_length": 532,
          "cds_start": 1446,
          "cds_end": null,
          "cds_length": 1599,
          "cdna_start": 1517,
          "cdna_end": null,
          "cdna_length": 2525,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "c.1296C>T",
          "hgvs_p": "p.Gly432Gly",
          "transcript": "NM_001363513.2",
          "protein_id": "NP_001350442.1",
          "transcript_support_level": null,
          "aa_start": 432,
          "aa_end": null,
          "aa_length": 482,
          "cds_start": 1296,
          "cds_end": null,
          "cds_length": 1449,
          "cdna_start": 1367,
          "cdna_end": null,
          "cdna_length": 2375,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "c.1296C>T",
          "hgvs_p": "p.Gly432Gly",
          "transcript": "ENST00000642044.1",
          "protein_id": "ENSP00000493232.1",
          "transcript_support_level": null,
          "aa_start": 432,
          "aa_end": null,
          "aa_length": 482,
          "cds_start": 1296,
          "cds_end": null,
          "cds_length": 1449,
          "cdna_start": 1419,
          "cdna_end": null,
          "cdna_length": 2221,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "c.1290C>T",
          "hgvs_p": "p.Gly430Gly",
          "transcript": "ENST00000635239.1",
          "protein_id": "ENSP00000489563.1",
          "transcript_support_level": 5,
          "aa_start": 430,
          "aa_end": null,
          "aa_length": 480,
          "cds_start": 1290,
          "cds_end": null,
          "cds_length": 1443,
          "cdna_start": 1413,
          "cdna_end": null,
          "cdna_length": 2215,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "c.1284C>T",
          "hgvs_p": "p.Gly428Gly",
          "transcript": "NM_006077.4",
          "protein_id": "NP_006068.2",
          "transcript_support_level": null,
          "aa_start": 428,
          "aa_end": null,
          "aa_length": 478,
          "cds_start": 1284,
          "cds_end": null,
          "cds_length": 1437,
          "cdna_start": 1355,
          "cdna_end": null,
          "cdna_length": 2363,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "c.1278C>T",
          "hgvs_p": "p.Gly426Gly",
          "transcript": "NM_001441220.1",
          "protein_id": "NP_001428149.1",
          "transcript_support_level": null,
          "aa_start": 426,
          "aa_end": null,
          "aa_length": 476,
          "cds_start": 1278,
          "cds_end": null,
          "cds_length": 1431,
          "cdna_start": 1465,
          "cdna_end": null,
          "cdna_length": 2473,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "c.1278C>T",
          "hgvs_p": "p.Gly426Gly",
          "transcript": "NM_001441221.1",
          "protein_id": "NP_001428150.1",
          "transcript_support_level": null,
          "aa_start": 426,
          "aa_end": null,
          "aa_length": 476,
          "cds_start": 1278,
          "cds_end": null,
          "cds_length": 1431,
          "cdna_start": 1483,
          "cdna_end": null,
          "cdna_length": 2491,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "c.1278C>T",
          "hgvs_p": "p.Gly426Gly",
          "transcript": "NM_001441222.1",
          "protein_id": "NP_001428151.1",
          "transcript_support_level": null,
          "aa_start": 426,
          "aa_end": null,
          "aa_length": 476,
          "cds_start": 1278,
          "cds_end": null,
          "cds_length": 1431,
          "cdna_start": 1443,
          "cdna_end": null,
          "cdna_length": 2451,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "c.1278C>T",
          "hgvs_p": "p.Gly426Gly",
          "transcript": "NM_001441223.1",
          "protein_id": "NP_001428152.1",
          "transcript_support_level": null,
          "aa_start": 426,
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          "cds_start": 1278,
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          "cdna_start": 1447,
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          "mane_select": null,
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          "biotype": null,
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        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
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          "exon_count": 12,
          "intron_rank": null,
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          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "c.1266C>T",
          "hgvs_p": "p.Gly422Gly",
          "transcript": "NM_001441224.1",
          "protein_id": "NP_001428153.1",
          "transcript_support_level": null,
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          "cds_start": 1266,
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          "cdna_start": 1337,
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          "cdna_length": 2345,
          "mane_select": null,
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        },
        {
          "aa_ref": "G",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "c.1188C>T",
          "hgvs_p": "p.Gly396Gly",
          "transcript": "NM_001441225.1",
          "protein_id": "NP_001428154.1",
          "transcript_support_level": null,
          "aa_start": 396,
          "aa_end": null,
          "aa_length": 446,
          "cds_start": 1188,
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          "cds_length": 1341,
          "cdna_start": 1259,
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          "mane_select": null,
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          "feature": null
        },
        {
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          "protein_coding": true,
          "strand": false,
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          ],
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          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "c.1179C>T",
          "hgvs_p": "p.Gly393Gly",
          "transcript": "NM_001441226.1",
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        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
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          "exon_count": 11,
          "intron_rank": null,
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          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "c.1155C>T",
          "hgvs_p": "p.Gly385Gly",
          "transcript": "NM_001441227.1",
          "protein_id": "NP_001428156.1",
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          "aa_end": null,
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          "cds_start": 1155,
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          "cdna_start": 1226,
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        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "c.945C>T",
          "hgvs_p": "p.Gly315Gly",
          "transcript": "NM_001441228.1",
          "protein_id": "NP_001428157.1",
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          "aa_start": 315,
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          "cds_start": 945,
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          "cdna_start": 1018,
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        },
        {
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "MICU1",
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          "hgvs_c": "c.882C>T",
          "hgvs_p": "p.Gly294Gly",
          "transcript": "NM_001441229.1",
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        {
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            "synonymous_variant"
          ],
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          "intron_rank": null,
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          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
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          "hgvs_p": "p.Gly261Gly",
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        },
        {
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          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 7,
          "intron_rank": null,
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          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "c.684C>T",
          "hgvs_p": "p.Gly228Gly",
          "transcript": "NM_001195519.2",
          "protein_id": "NP_001182448.1",
          "transcript_support_level": null,
          "aa_start": 228,
          "aa_end": null,
          "aa_length": 278,
          "cds_start": 684,
          "cds_end": null,
          "cds_length": 837,
          "cdna_start": 811,
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          "cdna_length": 1819,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MICU1",
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          "hgvs_c": "n.2501C>T",
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          "gene_symbol": "MICU1",
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        },
        {
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          "consequences": [
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          "intron_rank": null,
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          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
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        },
        {
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          "protein_coding": false,
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          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 10,
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          "exon_count": 10,
          "intron_rank": null,
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          "gene_symbol": "MICU1",
          "gene_hgnc_id": 1530,
          "hgvs_c": "n.*186C>T",
          "hgvs_p": null,
          "transcript": "ENST00000476605.7",
          "protein_id": "ENSP00000432492.3",
          "transcript_support_level": 2,
          "aa_start": null,
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          "cdna_start": null,
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          "cdna_length": 1933,
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          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "MICU1",
      "gene_hgnc_id": 1530,
      "dbsnp": "rs751988387",
      "frequency_reference_population": 0.000002480011,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 4,
      "gnomad_exomes_af": 0.00000205368,
      "gnomad_genomes_af": 0.00000657436,
      "gnomad_exomes_ac": 3,
      "gnomad_genomes_ac": 1,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.6800000071525574,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.68,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -1.053,
      "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": -5,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong,BP6_Moderate,BP7",
      "acmg_by_gene": [
        {
          "score": -5,
          "benign_score": 7,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP6_Moderate",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_001195518.2",
          "gene_symbol": "MICU1",
          "hgnc_id": 1530,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.1278C>T",
          "hgvs_p": "p.Gly426Gly"
        }
      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}