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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: 3-47017180-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=47017180&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "3",
      "pos": 47017180,
      "ref": "C",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "NM_014159.7",
      "consequences": [
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.7608G>T",
          "hgvs_p": "p.Val2536Val",
          "transcript": "NM_014159.7",
          "protein_id": "NP_054878.5",
          "transcript_support_level": null,
          "aa_start": 2536,
          "aa_end": null,
          "aa_length": 2564,
          "cds_start": 7608,
          "cds_end": null,
          "cds_length": 7695,
          "cdna_start": 7797,
          "cdna_end": null,
          "cdna_length": 8541,
          "mane_select": "ENST00000409792.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.7608G>T",
          "hgvs_p": "p.Val2536Val",
          "transcript": "ENST00000409792.4",
          "protein_id": "ENSP00000386759.3",
          "transcript_support_level": 5,
          "aa_start": 2536,
          "aa_end": null,
          "aa_length": 2564,
          "cds_start": 7608,
          "cds_end": null,
          "cds_length": 7695,
          "cdna_start": 7797,
          "cdna_end": null,
          "cdna_length": 8541,
          "mane_select": "NM_014159.7",
          "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": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*3331G>T",
          "hgvs_p": null,
          "transcript": "ENST00000330022.11",
          "protein_id": "ENSP00000332415.7",
          "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": 8172,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*3331G>T",
          "hgvs_p": null,
          "transcript": "ENST00000330022.11",
          "protein_id": "ENSP00000332415.7",
          "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": 8172,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.7476G>T",
          "hgvs_p": "p.Val2492Val",
          "transcript": "NM_001349370.3",
          "protein_id": "NP_001336299.1",
          "transcript_support_level": null,
          "aa_start": 2492,
          "aa_end": null,
          "aa_length": 2520,
          "cds_start": 7476,
          "cds_end": null,
          "cds_length": 7563,
          "cdna_start": 7781,
          "cdna_end": null,
          "cdna_length": 8525,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.7476G>T",
          "hgvs_p": "p.Val2492Val",
          "transcript": "ENST00000638947.2",
          "protein_id": "ENSP00000491413.2",
          "transcript_support_level": 5,
          "aa_start": 2492,
          "aa_end": null,
          "aa_length": 2520,
          "cds_start": 7476,
          "cds_end": null,
          "cds_length": 7563,
          "cdna_start": 7550,
          "cdna_end": null,
          "cdna_length": 8302,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.7374G>T",
          "hgvs_p": "p.Val2458Val",
          "transcript": "ENST00000685005.1",
          "protein_id": "ENSP00000509568.1",
          "transcript_support_level": null,
          "aa_start": 2458,
          "aa_end": null,
          "aa_length": 2486,
          "cds_start": 7374,
          "cds_end": null,
          "cds_length": 7461,
          "cdna_start": 7374,
          "cdna_end": null,
          "cdna_length": 8109,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.4323G>T",
          "hgvs_p": "p.Val1441Val",
          "transcript": "ENST00000686876.1",
          "protein_id": "ENSP00000509591.1",
          "transcript_support_level": null,
          "aa_start": 1441,
          "aa_end": null,
          "aa_length": 1469,
          "cds_start": 4323,
          "cds_end": null,
          "cds_length": 4410,
          "cdna_start": 4324,
          "cdna_end": null,
          "cdna_length": 5076,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.3960G>T",
          "hgvs_p": "p.Val1320Val",
          "transcript": "ENST00000690157.1",
          "protein_id": "ENSP00000509438.1",
          "transcript_support_level": null,
          "aa_start": 1320,
          "aa_end": null,
          "aa_length": 1348,
          "cds_start": 3960,
          "cds_end": null,
          "cds_length": 4047,
          "cdna_start": 3961,
          "cdna_end": null,
          "cdna_length": 4696,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "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": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.3402G>T",
          "hgvs_p": "p.Val1134Val",
          "transcript": "ENST00000691902.1",
          "protein_id": "ENSP00000510234.1",
          "transcript_support_level": null,
          "aa_start": 1134,
          "aa_end": null,
          "aa_length": 1162,
          "cds_start": 3402,
          "cds_end": null,
          "cds_length": 3489,
          "cdna_start": 3403,
          "cdna_end": null,
          "cdna_length": 4138,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "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": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.2664G>T",
          "hgvs_p": "p.Val888Val",
          "transcript": "ENST00000691544.1",
          "protein_id": "ENSP00000510710.1",
          "transcript_support_level": null,
          "aa_start": 888,
          "aa_end": null,
          "aa_length": 916,
          "cds_start": 2664,
          "cds_end": null,
          "cds_length": 2751,
          "cdna_start": 2664,
          "cdna_end": null,
          "cdna_length": 3416,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.7476G>T",
          "hgvs_p": "p.Val2492Val",
          "transcript": "XM_047448045.1",
          "protein_id": "XP_047304001.1",
          "transcript_support_level": null,
          "aa_start": 2492,
          "aa_end": null,
          "aa_length": 2520,
          "cds_start": 7476,
          "cds_end": null,
          "cds_length": 7563,
          "cdna_start": 7578,
          "cdna_end": null,
          "cdna_length": 8322,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.7341G>T",
          "hgvs_p": "p.Val2447Val",
          "transcript": "XM_024453487.2",
          "protein_id": "XP_024309255.1",
          "transcript_support_level": null,
          "aa_start": 2447,
          "aa_end": null,
          "aa_length": 2475,
          "cds_start": 7341,
          "cds_end": null,
          "cds_length": 7428,
          "cdna_start": 7443,
          "cdna_end": null,
          "cdna_length": 8187,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "V",
          "aa_alt": "V",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "c.7176G>T",
          "hgvs_p": "p.Val2392Val",
          "transcript": "XM_024453488.2",
          "protein_id": "XP_024309256.1",
          "transcript_support_level": null,
          "aa_start": 2392,
          "aa_end": null,
          "aa_length": 2420,
          "cds_start": 7176,
          "cds_end": null,
          "cds_length": 7263,
          "cdna_start": 7237,
          "cdna_end": null,
          "cdna_length": 7981,
          "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": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*2933G>T",
          "hgvs_p": null,
          "transcript": "ENST00000431180.5",
          "protein_id": "ENSP00000388349.1",
          "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": 7555,
          "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": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*1558G>T",
          "hgvs_p": null,
          "transcript": "ENST00000445387.5",
          "protein_id": "ENSP00000411901.1",
          "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": 7075,
          "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": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.4417G>T",
          "hgvs_p": null,
          "transcript": "ENST00000685237.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5152,
          "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": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*1814G>T",
          "hgvs_p": null,
          "transcript": "ENST00000685505.1",
          "protein_id": "ENSP00000510732.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6667,
          "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": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.*1714G>T",
          "hgvs_p": null,
          "transcript": "ENST00000686773.1",
          "protein_id": "ENSP00000510025.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 6508,
          "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": 10,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
          "hgvs_c": "n.1830G>T",
          "hgvs_p": null,
          "transcript": "ENST00000686792.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2565,
          "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": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SETD2",
          "gene_hgnc_id": 18420,
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}