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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: 21-33241949-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=21&pos=33241949&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "21",
      "pos": 33241949,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "ENST00000342136.9",
      "consequences": [
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2",
          "gene_hgnc_id": 5433,
          "hgvs_c": "c.27C>T",
          "hgvs_p": "p.Ile9Ile",
          "transcript": "NM_001289125.3",
          "protein_id": "NP_001276054.1",
          "transcript_support_level": null,
          "aa_start": 9,
          "aa_end": null,
          "aa_length": 515,
          "cds_start": 27,
          "cds_end": null,
          "cds_length": 1548,
          "cdna_start": 389,
          "cdna_end": null,
          "cdna_length": 4074,
          "mane_select": "ENST00000342136.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2",
          "gene_hgnc_id": 5433,
          "hgvs_c": "c.27C>T",
          "hgvs_p": "p.Ile9Ile",
          "transcript": "ENST00000342136.9",
          "protein_id": "ENSP00000343957.5",
          "transcript_support_level": 1,
          "aa_start": 9,
          "aa_end": null,
          "aa_length": 515,
          "cds_start": 27,
          "cds_end": null,
          "cds_length": 1548,
          "cdna_start": 389,
          "cdna_end": null,
          "cdna_length": 4074,
          "mane_select": "NM_001289125.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2-IL10RB",
          "gene_hgnc_id": null,
          "hgvs_c": "c.27C>T",
          "hgvs_p": "p.Ile9Ile",
          "transcript": "ENST00000433395.7",
          "protein_id": "ENSP00000388223.3",
          "transcript_support_level": 5,
          "aa_start": 9,
          "aa_end": null,
          "aa_length": 545,
          "cds_start": 27,
          "cds_end": null,
          "cds_length": 1638,
          "cdna_start": 150,
          "cdna_end": null,
          "cdna_length": 2112,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2",
          "gene_hgnc_id": 5433,
          "hgvs_c": "c.27C>T",
          "hgvs_p": "p.Ile9Ile",
          "transcript": "ENST00000382264.7",
          "protein_id": "ENSP00000371699.3",
          "transcript_support_level": 1,
          "aa_start": 9,
          "aa_end": null,
          "aa_length": 331,
          "cds_start": 27,
          "cds_end": null,
          "cds_length": 996,
          "cdna_start": 380,
          "cdna_end": null,
          "cdna_length": 1389,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2",
          "gene_hgnc_id": 5433,
          "hgvs_c": "c.27C>T",
          "hgvs_p": "p.Ile9Ile",
          "transcript": "ENST00000404220.7",
          "protein_id": "ENSP00000384309.2",
          "transcript_support_level": 1,
          "aa_start": 9,
          "aa_end": null,
          "aa_length": 331,
          "cds_start": 27,
          "cds_end": null,
          "cds_length": 996,
          "cdna_start": 356,
          "cdna_end": null,
          "cdna_length": 4284,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2",
          "gene_hgnc_id": 5433,
          "hgvs_c": "c.27C>T",
          "hgvs_p": "p.Ile9Ile",
          "transcript": "ENST00000342101.7",
          "protein_id": "ENSP00000343289.3",
          "transcript_support_level": 1,
          "aa_start": 9,
          "aa_end": null,
          "aa_length": 239,
          "cds_start": 27,
          "cds_end": null,
          "cds_length": 720,
          "cdna_start": 191,
          "cdna_end": null,
          "cdna_length": 2606,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2-IL10RB",
          "gene_hgnc_id": null,
          "hgvs_c": "c.27C>T",
          "hgvs_p": "p.Ile9Ile",
          "transcript": "NM_001414505.1",
          "protein_id": "NP_001401434.1",
          "transcript_support_level": null,
          "aa_start": 9,
          "aa_end": null,
          "aa_length": 545,
          "cds_start": 27,
          "cds_end": null,
          "cds_length": 1638,
          "cdna_start": 343,
          "cdna_end": null,
          "cdna_length": 2818,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2",
          "gene_hgnc_id": 5433,
          "hgvs_c": "c.27C>T",
          "hgvs_p": "p.Ile9Ile",
          "transcript": "NM_207585.3",
          "protein_id": "NP_997468.1",
          "transcript_support_level": null,
          "aa_start": 9,
          "aa_end": null,
          "aa_length": 515,
          "cds_start": 27,
          "cds_end": null,
          "cds_length": 1548,
          "cdna_start": 343,
          "cdna_end": null,
          "cdna_length": 4028,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2",
          "gene_hgnc_id": 5433,
          "hgvs_c": "c.27C>T",
          "hgvs_p": "p.Ile9Ile",
          "transcript": "ENST00000683941.1",
          "protein_id": "ENSP00000508013.1",
          "transcript_support_level": null,
          "aa_start": 9,
          "aa_end": null,
          "aa_length": 515,
          "cds_start": 27,
          "cds_end": null,
          "cds_length": 1548,
          "cdna_start": 187,
          "cdna_end": null,
          "cdna_length": 3872,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2",
          "gene_hgnc_id": 5433,
          "hgvs_c": "c.27C>T",
          "hgvs_p": "p.Ile9Ile",
          "transcript": "NM_001385055.1",
          "protein_id": "NP_001371984.1",
          "transcript_support_level": null,
          "aa_start": 9,
          "aa_end": null,
          "aa_length": 451,
          "cds_start": 27,
          "cds_end": null,
          "cds_length": 1356,
          "cdna_start": 343,
          "cdna_end": null,
          "cdna_length": 2365,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2",
          "gene_hgnc_id": 5433,
          "hgvs_c": "c.27C>T",
          "hgvs_p": "p.Ile9Ile",
          "transcript": "NM_000874.5",
          "protein_id": "NP_000865.2",
          "transcript_support_level": null,
          "aa_start": 9,
          "aa_end": null,
          "aa_length": 331,
          "cds_start": 27,
          "cds_end": null,
          "cds_length": 996,
          "cdna_start": 389,
          "cdna_end": null,
          "cdna_length": 4306,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2",
          "gene_hgnc_id": 5433,
          "hgvs_c": "c.27C>T",
          "hgvs_p": "p.Ile9Ile",
          "transcript": "NM_207584.3",
          "protein_id": "NP_997467.1",
          "transcript_support_level": null,
          "aa_start": 9,
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          "aa_length": 331,
          "cds_start": 27,
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          "cdna_start": 343,
          "cdna_end": null,
          "cdna_length": 4260,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2",
          "gene_hgnc_id": 5433,
          "hgvs_c": "c.27C>T",
          "hgvs_p": "p.Ile9Ile",
          "transcript": "NM_001385054.1",
          "protein_id": "NP_001371983.1",
          "transcript_support_level": null,
          "aa_start": 9,
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          "cds_start": 27,
          "cds_end": null,
          "cds_length": 726,
          "cdna_start": 343,
          "cdna_end": null,
          "cdna_length": 4129,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2",
          "gene_hgnc_id": 5433,
          "hgvs_c": "c.27C>T",
          "hgvs_p": "p.Ile9Ile",
          "transcript": "NM_001289126.2",
          "protein_id": "NP_001276055.1",
          "transcript_support_level": null,
          "aa_start": 9,
          "aa_end": null,
          "aa_length": 239,
          "cds_start": 27,
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          "cds_length": 720,
          "cdna_start": 343,
          "cdna_end": null,
          "cdna_length": 3897,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2",
          "gene_hgnc_id": 5433,
          "hgvs_c": "c.27C>T",
          "hgvs_p": "p.Ile9Ile",
          "transcript": "NM_001289128.2",
          "protein_id": "NP_001276057.1",
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          "cdna_start": 389,
          "cdna_end": null,
          "cdna_length": 3943,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "I",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2",
          "gene_hgnc_id": 5433,
          "hgvs_c": "c.99C>T",
          "hgvs_p": "p.Ile33Ile",
          "transcript": "ENST00000447980.1",
          "protein_id": "ENSP00000402311.1",
          "transcript_support_level": 5,
          "aa_start": 33,
          "aa_end": null,
          "aa_length": 203,
          "cds_start": 99,
          "cds_end": null,
          "cds_length": 612,
          "cdna_start": 213,
          "cdna_end": null,
          "cdna_length": 726,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2",
          "gene_hgnc_id": 5433,
          "hgvs_c": "n.27C>T",
          "hgvs_p": null,
          "transcript": "ENST00000382238.6",
          "protein_id": "ENSP00000371673.2",
          "transcript_support_level": 3,
          "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": 1127,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2",
          "gene_hgnc_id": 5433,
          "hgvs_c": "n.299C>T",
          "hgvs_p": null,
          "transcript": "ENST00000420068.1",
          "protein_id": null,
          "transcript_support_level": 5,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 505,
          "mane_select": null,
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          "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": 2,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2-IL10RB",
          "gene_hgnc_id": null,
          "hgvs_c": "n.27C>T",
          "hgvs_p": null,
          "transcript": "ENST00000646150.1",
          "protein_id": "ENSP00000496248.1",
          "transcript_support_level": null,
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          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 3770,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2-IL10RB",
          "gene_hgnc_id": null,
          "hgvs_c": "n.27C>T",
          "hgvs_p": null,
          "transcript": "ENST00000682009.1",
          "protein_id": "ENSP00000506919.1",
          "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": 2941,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "IFNAR2-IL10RB",
          "gene_hgnc_id": null,
          "hgvs_c": "n.27C>T",
          "hgvs_p": null,
          "transcript": "ENST00000683116.1",
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        {
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          "protein_coding": false,
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        },
        {
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          "protein_coding": false,
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
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          ],
          "exon_rank": null,
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          "exon_count": 7,
          "intron_rank": 1,
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          "gene_symbol": "IFNAR2",
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          "hgvs_c": "c.-119-3002C>T",
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          "transcript": "ENST00000443073.5",
          "protein_id": "ENSP00000403569.1",
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          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 841,
          "mane_select": null,
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          "feature": null
        },
        {
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          "strand": true,
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          ],
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          "gene_symbol": "IFNAR2",
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          "hgvs_c": "c.-119-3002C>T",
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          "transcript": "ENST00000413881.5",
          "protein_id": "ENSP00000413160.1",
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          "aa_start": null,
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          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 710,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "IFNAR2",
      "gene_hgnc_id": 5433,
      "dbsnp": "rs750264158",
      "frequency_reference_population": 0.0000027385743,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 4,
      "gnomad_exomes_af": 0.00000273857,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 4,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.800000011920929,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.3700000047683716,
      "splice_prediction_selected": "Uncertain_significance",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.8,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -1.404,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.37,
      "spliceai_max_prediction": "Uncertain_significance",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": 2,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2",
      "acmg_by_gene": [
        {
          "score": 2,
          "benign_score": 0,
          "pathogenic_score": 2,
          "criteria": [
            "PM2"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000342136.9",
          "gene_symbol": "IFNAR2",
          "hgnc_id": 5433,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.27C>T",
          "hgvs_p": "p.Ile9Ile"
        },
        {
          "score": 2,
          "benign_score": 0,
          "pathogenic_score": 2,
          "criteria": [
            "PM2"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000433395.7",
          "gene_symbol": "IFNAR2-IL10RB",
          "hgnc_id": null,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "c.27C>T",
          "hgvs_p": "p.Ile9Ile"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}