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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: 11-9790561-T-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=9790561&ref=T&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 9790561,
      "ref": "T",
      "alt": "G",
      "effect": "missense_variant",
      "transcript": "ENST00000256190.13",
      "consequences": [
        {
          "aa_ref": "I",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 34,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4693A>C",
          "hgvs_p": "p.Ile1565Leu",
          "transcript": "NM_030962.4",
          "protein_id": "NP_112224.1",
          "transcript_support_level": null,
          "aa_start": 1565,
          "aa_end": null,
          "aa_length": 1849,
          "cds_start": 4693,
          "cds_end": null,
          "cds_length": 5550,
          "cdna_start": 4843,
          "cdna_end": null,
          "cdna_length": 7450,
          "mane_select": "ENST00000256190.13",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "L",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 34,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4693A>C",
          "hgvs_p": "p.Ile1565Leu",
          "transcript": "ENST00000256190.13",
          "protein_id": "ENSP00000256190.8",
          "transcript_support_level": 1,
          "aa_start": 1565,
          "aa_end": null,
          "aa_length": 1849,
          "cds_start": 4693,
          "cds_end": null,
          "cds_length": 5550,
          "cdna_start": 4843,
          "cdna_end": null,
          "cdna_length": 7450,
          "mane_select": "NM_030962.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 35,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4789A>C",
          "hgvs_p": "p.Ile1597Leu",
          "transcript": "NM_001386339.1",
          "protein_id": "NP_001373268.1",
          "transcript_support_level": null,
          "aa_start": 1597,
          "aa_end": null,
          "aa_length": 1881,
          "cds_start": 4789,
          "cds_end": null,
          "cds_length": 5646,
          "cdna_start": 4939,
          "cdna_end": null,
          "cdna_length": 7546,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 35,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4789A>C",
          "hgvs_p": "p.Ile1597Leu",
          "transcript": "ENST00000689128.1",
          "protein_id": "ENSP00000509587.1",
          "transcript_support_level": null,
          "aa_start": 1597,
          "aa_end": null,
          "aa_length": 1881,
          "cds_start": 4789,
          "cds_end": null,
          "cds_length": 5646,
          "cdna_start": 4848,
          "cdna_end": null,
          "cdna_length": 7279,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 35,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4768A>C",
          "hgvs_p": "p.Ile1590Leu",
          "transcript": "ENST00000675281.2",
          "protein_id": "ENSP00000502491.1",
          "transcript_support_level": null,
          "aa_start": 1590,
          "aa_end": null,
          "aa_length": 1874,
          "cds_start": 4768,
          "cds_end": null,
          "cds_length": 5625,
          "cdna_start": 4918,
          "cdna_end": null,
          "cdna_length": 7347,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 35,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4750A>C",
          "hgvs_p": "p.Ile1584Leu",
          "transcript": "ENST00000676387.2",
          "protein_id": "ENSP00000502779.1",
          "transcript_support_level": null,
          "aa_start": 1584,
          "aa_end": null,
          "aa_length": 1868,
          "cds_start": 4750,
          "cds_end": null,
          "cds_length": 5607,
          "cdna_start": 4888,
          "cdna_end": null,
          "cdna_length": 7167,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 35,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4729A>C",
          "hgvs_p": "p.Ile1577Leu",
          "transcript": "NM_001424318.1",
          "protein_id": "NP_001411247.1",
          "transcript_support_level": null,
          "aa_start": 1577,
          "aa_end": null,
          "aa_length": 1861,
          "cds_start": 4729,
          "cds_end": null,
          "cds_length": 5586,
          "cdna_start": 5273,
          "cdna_end": null,
          "cdna_length": 7880,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 35,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4729A>C",
          "hgvs_p": "p.Ile1577Leu",
          "transcript": "NM_001425070.1",
          "protein_id": "NP_001411999.1",
          "transcript_support_level": null,
          "aa_start": 1577,
          "aa_end": null,
          "aa_length": 1861,
          "cds_start": 4729,
          "cds_end": null,
          "cds_length": 5586,
          "cdna_start": 5073,
          "cdna_end": null,
          "cdna_length": 7680,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 34,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4687A>C",
          "hgvs_p": "p.Ile1563Leu",
          "transcript": "ENST00000689940.1",
          "protein_id": "ENSP00000508452.1",
          "transcript_support_level": null,
          "aa_start": 1563,
          "aa_end": null,
          "aa_length": 1847,
          "cds_start": 4687,
          "cds_end": null,
          "cds_length": 5544,
          "cdna_start": 4845,
          "cdna_end": null,
          "cdna_length": 7452,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 34,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4630A>C",
          "hgvs_p": "p.Ile1544Leu",
          "transcript": "ENST00000689258.1",
          "protein_id": "ENSP00000510475.1",
          "transcript_support_level": null,
          "aa_start": 1544,
          "aa_end": null,
          "aa_length": 1828,
          "cds_start": 4630,
          "cds_end": null,
          "cds_length": 5487,
          "cdna_start": 4771,
          "cdna_end": null,
          "cdna_length": 6667,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 34,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4588A>C",
          "hgvs_p": "p.Ile1530Leu",
          "transcript": "NM_001425069.1",
          "protein_id": "NP_001411998.1",
          "transcript_support_level": null,
          "aa_start": 1530,
          "aa_end": null,
          "aa_length": 1814,
          "cds_start": 4588,
          "cds_end": null,
          "cds_length": 5445,
          "cdna_start": 4932,
          "cdna_end": null,
          "cdna_length": 7539,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 33,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4564A>C",
          "hgvs_p": "p.Ile1522Leu",
          "transcript": "NM_001386342.1",
          "protein_id": "NP_001373271.1",
          "transcript_support_level": null,
          "aa_start": 1522,
          "aa_end": null,
          "aa_length": 1806,
          "cds_start": 4564,
          "cds_end": null,
          "cds_length": 5421,
          "cdna_start": 4714,
          "cdna_end": null,
          "cdna_length": 7321,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 33,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4564A>C",
          "hgvs_p": "p.Ile1522Leu",
          "transcript": "ENST00000692716.1",
          "protein_id": "ENSP00000509545.1",
          "transcript_support_level": null,
          "aa_start": 1522,
          "aa_end": null,
          "aa_length": 1806,
          "cds_start": 4564,
          "cds_end": null,
          "cds_length": 5421,
          "cdna_start": 4716,
          "cdna_end": null,
          "cdna_length": 9215,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "L",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 36,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4300A>C",
          "hgvs_p": "p.Ile1434Leu",
          "transcript": "ENST00000688344.1",
          "protein_id": "ENSP00000509987.1",
          "transcript_support_level": null,
          "aa_start": 1434,
          "aa_end": null,
          "aa_length": 1718,
          "cds_start": 4300,
          "cds_end": null,
          "cds_length": 5157,
          "cdna_start": 4300,
          "cdna_end": null,
          "cdna_length": 6763,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.3397A>C",
          "hgvs_p": "p.Ile1133Leu",
          "transcript": "ENST00000689597.1",
          "protein_id": "ENSP00000510781.1",
          "transcript_support_level": null,
          "aa_start": 1133,
          "aa_end": null,
          "aa_length": 1312,
          "cds_start": 3397,
          "cds_end": null,
          "cds_length": 3939,
          "cdna_start": 3397,
          "cdna_end": null,
          "cdna_length": 4133,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "N",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 34,
          "exon_rank_end": null,
          "exon_count": 35,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "c.4662A>C",
          "hgvs_p": "p.Lys1554Asn",
          "transcript": "XM_047427657.1",
          "protein_id": "XP_047283613.1",
          "transcript_support_level": null,
          "aa_start": 1554,
          "aa_end": null,
          "aa_length": 1554,
          "cds_start": 4662,
          "cds_end": null,
          "cds_length": 4665,
          "cdna_start": 4812,
          "cdna_end": null,
          "cdna_length": 4925,
          "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": 7,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "n.1177A>C",
          "hgvs_p": null,
          "transcript": "ENST00000524961.6",
          "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": 3559,
          "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": 6,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "n.1229A>C",
          "hgvs_p": null,
          "transcript": "ENST00000532095.2",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
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          "cdna_start": null,
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          "cdna_length": 1866,
          "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": 36,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "n.*1001A>C",
          "hgvs_p": null,
          "transcript": "ENST00000676324.2",
          "protein_id": "ENSP00000502578.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 7085,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SBF2",
          "gene_hgnc_id": 2135,
          "hgvs_c": "n.*386A>C",
          "hgvs_p": null,
          "transcript": "ENST00000689342.1",
          "protein_id": "ENSP00000510508.1",
          "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": 3239,
          "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": 16,
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        {
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      ],
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      "hom_count_reference_population": 0,
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      "gnomad_exomes_af": 0.00000139697,
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      "gnomad_exomes_ac": 2,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
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      "computational_score_selected": 0.1151396632194519,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0.15000000596046448,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.118,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.0856,
      "alphamissense_prediction": "Benign",
      "bayesdelnoaf_score": -0.38,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 1.197,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.15,
      "spliceai_max_prediction": "Benign",
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      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
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      "acmg_score": 0,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2,BP4_Moderate",
      "acmg_by_gene": [
        {
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          "pathogenic_score": 2,
          "criteria": [
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            "BP4_Moderate"
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          "verdict": "Uncertain_significance",
          "transcript": "ENST00000256190.13",
          "gene_symbol": "SBF2",
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            "missense_variant"
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          "inheritance_mode": "AR",
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          "hgvs_p": "p.Ile1565Leu"
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        {
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          "pathogenic_score": 2,
          "criteria": [
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            "BP4_Moderate"
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          "verdict": "Uncertain_significance",
          "transcript": "ENST00000534671.1",
          "gene_symbol": "SBF2-AS1",
          "hgnc_id": 27438,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.235+9986T>G",
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        {
          "score": 0,
          "benign_score": 2,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "NR_188521.1",
          "gene_symbol": "LOC105369149",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.100-308T>G",
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      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}