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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: 19-49860027-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=49860027&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "19",
      "pos": 49860027,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "ENST00000391842.6",
      "consequences": [
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "c.1083C>T",
          "hgvs_p": "p.Ile361Ile",
          "transcript": "ENST00000391842.6",
          "protein_id": "ENSP00000375717.1",
          "transcript_support_level": 5,
          "aa_start": 361,
          "aa_end": null,
          "aa_length": 416,
          "cds_start": 1083,
          "cds_end": null,
          "cds_length": 1251,
          "cdna_start": 1253,
          "cdna_end": null,
          "cdna_length": 1884,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "c.1083C>T",
          "hgvs_p": "p.Ile361Ile",
          "transcript": "ENST00000599732.5",
          "protein_id": "ENSP00000469128.1",
          "transcript_support_level": 1,
          "aa_start": 361,
          "aa_end": null,
          "aa_length": 416,
          "cds_start": 1083,
          "cds_end": null,
          "cds_length": 1251,
          "cdna_start": 1221,
          "cdna_end": null,
          "cdna_length": 1577,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "c.1083C>T",
          "hgvs_p": "p.Ile361Ile",
          "transcript": "ENST00000601675.5",
          "protein_id": "ENSP00000472816.1",
          "transcript_support_level": 1,
          "aa_start": 361,
          "aa_end": null,
          "aa_length": 416,
          "cds_start": 1083,
          "cds_end": null,
          "cds_length": 1251,
          "cdna_start": 1187,
          "cdna_end": null,
          "cdna_length": 1587,
          "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": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "n.1364C>T",
          "hgvs_p": null,
          "transcript": "ENST00000597793.5",
          "protein_id": null,
          "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": 1716,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "c.946-29C>T",
          "hgvs_p": null,
          "transcript": "ENST00000600603.5",
          "protein_id": "ENSP00000471458.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 374,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1125,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1443,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "c.1128C>T",
          "hgvs_p": "p.Ile376Ile",
          "transcript": "NM_001364747.2",
          "protein_id": "NP_001351676.1",
          "transcript_support_level": null,
          "aa_start": 376,
          "aa_end": null,
          "aa_length": 431,
          "cds_start": 1128,
          "cds_end": null,
          "cds_length": 1296,
          "cdna_start": 1304,
          "cdna_end": null,
          "cdna_length": 1658,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "c.1128C>T",
          "hgvs_p": "p.Ile376Ile",
          "transcript": "NM_001364749.2",
          "protein_id": "NP_001351678.1",
          "transcript_support_level": null,
          "aa_start": 376,
          "aa_end": null,
          "aa_length": 431,
          "cds_start": 1128,
          "cds_end": null,
          "cds_length": 1296,
          "cdna_start": 1304,
          "cdna_end": null,
          "cdna_length": 1706,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "c.1083C>T",
          "hgvs_p": "p.Ile361Ile",
          "transcript": "NM_001305105.2",
          "protein_id": "NP_001292034.1",
          "transcript_support_level": null,
          "aa_start": 361,
          "aa_end": null,
          "aa_length": 416,
          "cds_start": 1083,
          "cds_end": null,
          "cds_length": 1251,
          "cdna_start": 1253,
          "cdna_end": null,
          "cdna_length": 1607,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "c.1083C>T",
          "hgvs_p": "p.Ile361Ile",
          "transcript": "NM_001394010.1",
          "protein_id": "NP_001380939.1",
          "transcript_support_level": null,
          "aa_start": 361,
          "aa_end": null,
          "aa_length": 416,
          "cds_start": 1083,
          "cds_end": null,
          "cds_length": 1251,
          "cdna_start": 1253,
          "cdna_end": null,
          "cdna_length": 1884,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "c.1083C>T",
          "hgvs_p": "p.Ile361Ile",
          "transcript": "NM_017432.5",
          "protein_id": "NP_059128.2",
          "transcript_support_level": null,
          "aa_start": 361,
          "aa_end": null,
          "aa_length": 416,
          "cds_start": 1083,
          "cds_end": null,
          "cds_length": 1251,
          "cdna_start": 1253,
          "cdna_end": null,
          "cdna_length": 1655,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "c.987C>T",
          "hgvs_p": "p.Ile329Ile",
          "transcript": "NM_001364745.2",
          "protein_id": "NP_001351674.1",
          "transcript_support_level": null,
          "aa_start": 329,
          "aa_end": null,
          "aa_length": 384,
          "cds_start": 987,
          "cds_end": null,
          "cds_length": 1155,
          "cdna_start": 1163,
          "cdna_end": null,
          "cdna_length": 1517,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "c.987C>T",
          "hgvs_p": "p.Ile329Ile",
          "transcript": "ENST00000601638.5",
          "protein_id": "ENSP00000469541.1",
          "transcript_support_level": 5,
          "aa_start": 329,
          "aa_end": null,
          "aa_length": 384,
          "cds_start": 987,
          "cds_end": null,
          "cds_length": 1155,
          "cdna_start": 1040,
          "cdna_end": null,
          "cdna_length": 1413,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "c.660C>T",
          "hgvs_p": "p.Ile220Ile",
          "transcript": "NM_001364748.2",
          "protein_id": "NP_001351677.1",
          "transcript_support_level": null,
          "aa_start": 220,
          "aa_end": null,
          "aa_length": 275,
          "cds_start": 660,
          "cds_end": null,
          "cds_length": 828,
          "cdna_start": 1129,
          "cdna_end": null,
          "cdna_length": 1531,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "c.660C>T",
          "hgvs_p": "p.Ile220Ile",
          "transcript": "NM_001364750.2",
          "protein_id": "NP_001351679.1",
          "transcript_support_level": null,
          "aa_start": 220,
          "aa_end": null,
          "aa_length": 275,
          "cds_start": 660,
          "cds_end": null,
          "cds_length": 828,
          "cdna_start": 1129,
          "cdna_end": null,
          "cdna_length": 1483,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PNKP",
          "gene_hgnc_id": 9154,
          "hgvs_c": "n.403G>A",
          "hgvs_p": null,
          "transcript": "ENST00000596624.1",
          "protein_id": null,
          "transcript_support_level": 4,
          "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": 548,
          "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": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "n.1101C>T",
          "hgvs_p": null,
          "transcript": "ENST00000598325.5",
          "protein_id": null,
          "transcript_support_level": 5,
          "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": 1438,
          "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": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "n.*268C>T",
          "hgvs_p": null,
          "transcript": "ENST00000601612.5",
          "protein_id": "ENSP00000470007.1",
          "transcript_support_level": 2,
          "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": 1480,
          "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": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "n.1158C>T",
          "hgvs_p": null,
          "transcript": "NR_130963.2",
          "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": 1512,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "n.*268C>T",
          "hgvs_p": null,
          "transcript": "ENST00000601612.5",
          "protein_id": "ENSP00000470007.1",
          "transcript_support_level": 2,
          "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": 1480,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "c.*115C>T",
          "hgvs_p": null,
          "transcript": "XM_047438940.1",
          "protein_id": "XP_047294896.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 366,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1101,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1424,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "PTOV1",
          "gene_hgnc_id": 9632,
          "hgvs_c": "c.946-29C>T",
          "hgvs_p": null,
          "transcript": "NM_001305108.2",
          "protein_id": "NP_001292037.1",
          "transcript_support_level": null,
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        },
        {
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          "exon_count": 6,
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        },
        {
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          "protein_coding": true,
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          "consequences": [
            "upstream_gene_variant"
          ],
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          "exon_count": 2,
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          "gene_symbol": "PTOV1",
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          "hgvs_c": "c.-112C>T",
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          "transcript": "ENST00000597730.1",
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        },
        {
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          "protein_coding": true,
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          "exon_count": 2,
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          "gene_symbol": "PNKP",
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          "hgvs_c": "c.*72G>A",
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          "transcript": "ENST00000636840.1",
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      ],
      "gene_symbol": "PTOV1",
      "gene_hgnc_id": 9632,
      "dbsnp": "rs878894160",
      "frequency_reference_population": 0.0000020521773,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 3,
      "gnomad_exomes_af": 0.00000205218,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 3,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.46000000834465027,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.07999999821186066,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.46,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -0.34,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.08,
      "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": -1,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Moderate,BP7",
      "acmg_by_gene": [
        {
          "score": -1,
          "benign_score": 3,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000391842.6",
          "gene_symbol": "PTOV1",
          "hgnc_id": 9632,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.1083C>T",
          "hgvs_p": "p.Ile361Ile"
        },
        {
          "score": 0,
          "benign_score": 2,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000596624.1",
          "gene_symbol": "PNKP",
          "hgnc_id": 9154,
          "effects": [
            "non_coding_transcript_exon_variant"
          ],
          "inheritance_mode": "AR,AD",
          "hgvs_c": "n.403G>A",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}