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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: 11-66565840-AG-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=66565840&ref=AG&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 66565840,
      "ref": "AG",
      "alt": "A",
      "effect": "frameshift_variant",
      "transcript": "ENST00000310325.10",
      "consequences": [
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "c.954delC",
          "hgvs_p": "p.Ser319fs",
          "transcript": "NM_003793.4",
          "protein_id": "NP_003784.2",
          "transcript_support_level": null,
          "aa_start": 318,
          "aa_end": null,
          "aa_length": 484,
          "cds_start": 954,
          "cds_end": null,
          "cds_length": 1455,
          "cdna_start": 1074,
          "cdna_end": null,
          "cdna_length": 2044,
          "mane_select": "ENST00000310325.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "c.954delC",
          "hgvs_p": "p.Ser319fs",
          "transcript": "ENST00000310325.10",
          "protein_id": "ENSP00000310832.5",
          "transcript_support_level": 1,
          "aa_start": 318,
          "aa_end": null,
          "aa_length": 484,
          "cds_start": 954,
          "cds_end": null,
          "cds_length": 1455,
          "cdna_start": 1074,
          "cdna_end": null,
          "cdna_length": 2044,
          "mane_select": "NM_003793.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "c.954delC",
          "hgvs_p": "p.Ser319fs",
          "transcript": "ENST00000679347.1",
          "protein_id": "ENSP00000503676.1",
          "transcript_support_level": null,
          "aa_start": 318,
          "aa_end": null,
          "aa_length": 505,
          "cds_start": 954,
          "cds_end": null,
          "cds_length": 1518,
          "cdna_start": 1074,
          "cdna_end": null,
          "cdna_length": 2139,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "c.954delC",
          "hgvs_p": "p.Ser319fs",
          "transcript": "ENST00000677005.1",
          "protein_id": "ENSP00000503238.1",
          "transcript_support_level": null,
          "aa_start": 318,
          "aa_end": null,
          "aa_length": 504,
          "cds_start": 954,
          "cds_end": null,
          "cds_length": 1515,
          "cdna_start": 1074,
          "cdna_end": null,
          "cdna_length": 2136,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "c.996delC",
          "hgvs_p": "p.Ser333fs",
          "transcript": "ENST00000677587.1",
          "protein_id": "ENSP00000503791.1",
          "transcript_support_level": null,
          "aa_start": 332,
          "aa_end": null,
          "aa_length": 498,
          "cds_start": 996,
          "cds_end": null,
          "cds_length": 1497,
          "cdna_start": 1116,
          "cdna_end": null,
          "cdna_length": 2086,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "c.954delC",
          "hgvs_p": "p.Ser319fs",
          "transcript": "ENST00000678872.1",
          "protein_id": "ENSP00000503425.1",
          "transcript_support_level": null,
          "aa_start": 318,
          "aa_end": null,
          "aa_length": 492,
          "cds_start": 954,
          "cds_end": null,
          "cds_length": 1479,
          "cdna_start": 1074,
          "cdna_end": null,
          "cdna_length": 2036,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "c.951delC",
          "hgvs_p": "p.Ser318fs",
          "transcript": "ENST00000524994.6",
          "protein_id": "ENSP00000433082.2",
          "transcript_support_level": 5,
          "aa_start": 317,
          "aa_end": null,
          "aa_length": 483,
          "cds_start": 951,
          "cds_end": null,
          "cds_length": 1452,
          "cdna_start": 1071,
          "cdna_end": null,
          "cdna_length": 1709,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "c.954delC",
          "hgvs_p": "p.Ser319fs",
          "transcript": "ENST00000678471.1",
          "protein_id": "ENSP00000502949.1",
          "transcript_support_level": null,
          "aa_start": 318,
          "aa_end": null,
          "aa_length": 483,
          "cds_start": 954,
          "cds_end": null,
          "cds_length": 1452,
          "cdna_start": 1074,
          "cdna_end": null,
          "cdna_length": 2014,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "c.945delC",
          "hgvs_p": "p.Ser316fs",
          "transcript": "ENST00000677896.1",
          "protein_id": "ENSP00000504605.1",
          "transcript_support_level": null,
          "aa_start": 315,
          "aa_end": null,
          "aa_length": 481,
          "cds_start": 945,
          "cds_end": null,
          "cds_length": 1446,
          "cdna_start": 1065,
          "cdna_end": null,
          "cdna_length": 2035,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "c.954delC",
          "hgvs_p": "p.Ser319fs",
          "transcript": "ENST00000679024.1",
          "protein_id": "ENSP00000503506.1",
          "transcript_support_level": null,
          "aa_start": 318,
          "aa_end": null,
          "aa_length": 479,
          "cds_start": 954,
          "cds_end": null,
          "cds_length": 1440,
          "cdna_start": 1074,
          "cdna_end": null,
          "cdna_length": 2061,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "c.882delC",
          "hgvs_p": "p.Ser295fs",
          "transcript": "ENST00000678305.1",
          "protein_id": "ENSP00000504383.1",
          "transcript_support_level": null,
          "aa_start": 294,
          "aa_end": null,
          "aa_length": 460,
          "cds_start": 882,
          "cds_end": null,
          "cds_length": 1383,
          "cdna_start": 1001,
          "cdna_end": null,
          "cdna_length": 1971,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "c.879delC",
          "hgvs_p": "p.Ser294fs",
          "transcript": "ENST00000679160.1",
          "protein_id": "ENSP00000503972.1",
          "transcript_support_level": null,
          "aa_start": 293,
          "aa_end": null,
          "aa_length": 459,
          "cds_start": 879,
          "cds_end": null,
          "cds_length": 1380,
          "cdna_start": 968,
          "cdna_end": null,
          "cdna_length": 1938,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "c.678delC",
          "hgvs_p": "p.Ser227fs",
          "transcript": "ENST00000526010.2",
          "protein_id": "ENSP00000435822.2",
          "transcript_support_level": 4,
          "aa_start": 226,
          "aa_end": null,
          "aa_length": 392,
          "cds_start": 678,
          "cds_end": null,
          "cds_length": 1179,
          "cdna_start": 903,
          "cdna_end": null,
          "cdna_length": 1873,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "c.774delC",
          "hgvs_p": "p.Ser259fs",
          "transcript": "XM_011545328.3",
          "protein_id": "XP_011543630.1",
          "transcript_support_level": null,
          "aa_start": 258,
          "aa_end": null,
          "aa_length": 424,
          "cds_start": 774,
          "cds_end": null,
          "cds_length": 1275,
          "cdna_start": 1177,
          "cdna_end": null,
          "cdna_length": 2147,
          "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": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "n.*148delC",
          "hgvs_p": null,
          "transcript": "ENST00000525733.6",
          "protein_id": "ENSP00000434936.2",
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
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          "cdna_start": null,
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          "cdna_length": 1439,
          "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": 7,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "n.853delC",
          "hgvs_p": null,
          "transcript": "ENST00000527141.6",
          "protein_id": null,
          "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": 2207,
          "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": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "n.214delC",
          "hgvs_p": null,
          "transcript": "ENST00000529199.1",
          "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": 578,
          "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": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "n.577delC",
          "hgvs_p": null,
          "transcript": "ENST00000530565.6",
          "protein_id": null,
          "transcript_support_level": 5,
          "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": 2940,
          "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": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "n.1042delC",
          "hgvs_p": null,
          "transcript": "ENST00000533168.2",
          "protein_id": null,
          "transcript_support_level": 2,
          "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": 1806,
          "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": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "n.905delC",
          "hgvs_p": null,
          "transcript": "ENST00000676860.1",
          "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": 2262,
          "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": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "n.954delC",
          "hgvs_p": null,
          "transcript": "ENST00000676924.1",
          "protein_id": "ENSP00000503579.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
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          "cdna_end": null,
          "cdna_length": 1475,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CTSF",
          "gene_hgnc_id": 2531,
          "hgvs_c": "n.-250delC",
          "hgvs_p": null,
          "transcript": "ENST00000677020.1",
          "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": 1941,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "CTSF",
      "gene_hgnc_id": 2531,
      "dbsnp": "rs753084727",
      "frequency_reference_population": 0.00007063836,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 114,
      "gnomad_exomes_af": 0.000076626,
      "gnomad_genomes_af": 0.0000131397,
      "gnomad_exomes_ac": 112,
      "gnomad_genomes_ac": 2,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": null,
      "computational_prediction_selected": null,
      "computational_source_selected": null,
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": null,
      "bayesdelnoaf_prediction": null,
      "phylop100way_score": 0.105,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": 11,
      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1,PM2,PP5",
      "acmg_by_gene": [
        {
          "score": 11,
          "benign_score": 0,
          "pathogenic_score": 11,
          "criteria": [
            "PVS1",
            "PM2",
            "PP5"
          ],
          "verdict": "Pathogenic",
          "transcript": "ENST00000310325.10",
          "gene_symbol": "CTSF",
          "hgnc_id": 2531,
          "effects": [
            "frameshift_variant"
          ],
          "inheritance_mode": "AR,Unknown",
          "hgvs_c": "c.954delC",
          "hgvs_p": "p.Ser319fs"
        }
      ],
      "clinvar_disease": "Neuronal ceroid lipofuscinosis 13",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "no assertion criteria provided",
      "clinvar_submissions_summary": "null",
      "phenotype_combined": "Neuronal ceroid lipofuscinosis 13",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}