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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: 12-112486563-TC-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=112486563&ref=TC&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "12",
      "pos": 112486563,
      "ref": "TC",
      "alt": "T",
      "effect": "frameshift_variant",
      "transcript": "NM_001330437.2",
      "consequences": [
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.1315delC",
          "hgvs_p": "p.Leu439fs",
          "transcript": "NM_002834.5",
          "protein_id": "NP_002825.3",
          "transcript_support_level": null,
          "aa_start": 439,
          "aa_end": null,
          "aa_length": 593,
          "cds_start": 1315,
          "cds_end": null,
          "cds_length": 1782,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000351677.7",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_002834.5"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.1315delC",
          "hgvs_p": "p.Leu439fs",
          "transcript": "ENST00000351677.7",
          "protein_id": "ENSP00000340944.3",
          "transcript_support_level": 1,
          "aa_start": 439,
          "aa_end": null,
          "aa_length": 593,
          "cds_start": 1315,
          "cds_end": null,
          "cds_length": 1782,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_002834.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000351677.7"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.1327delC",
          "hgvs_p": "p.Leu443fs",
          "transcript": "ENST00000635625.1",
          "protein_id": "ENSP00000489597.1",
          "transcript_support_level": 5,
          "aa_start": 443,
          "aa_end": null,
          "aa_length": 597,
          "cds_start": 1327,
          "cds_end": null,
          "cds_length": 1794,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000635625.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.1315delC",
          "hgvs_p": "p.Leu439fs",
          "transcript": "ENST00000392597.5",
          "protein_id": "ENSP00000376376.1",
          "transcript_support_level": 1,
          "aa_start": 439,
          "aa_end": null,
          "aa_length": 460,
          "cds_start": 1315,
          "cds_end": null,
          "cds_length": 1383,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000392597.5"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.328delC",
          "hgvs_p": "p.Leu110fs",
          "transcript": "ENST00000635652.1",
          "protein_id": "ENSP00000489541.1",
          "transcript_support_level": 3,
          "aa_start": 110,
          "aa_end": null,
          "aa_length": 195,
          "cds_start": 328,
          "cds_end": null,
          "cds_length": 588,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000635652.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.1315delC",
          "hgvs_p": "p.Leu439fs",
          "transcript": "ENST00000690210.1",
          "protein_id": "ENSP00000509272.1",
          "transcript_support_level": null,
          "aa_start": 439,
          "aa_end": null,
          "aa_length": 671,
          "cds_start": 1315,
          "cds_end": null,
          "cds_length": 2016,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000690210.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.1327delC",
          "hgvs_p": "p.Leu443fs",
          "transcript": "NM_001330437.2",
          "protein_id": "NP_001317366.1",
          "transcript_support_level": null,
          "aa_start": 443,
          "aa_end": null,
          "aa_length": 597,
          "cds_start": 1327,
          "cds_end": null,
          "cds_length": 1794,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001330437.2"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.1324delC",
          "hgvs_p": "p.Leu442fs",
          "transcript": "ENST00000882517.1",
          "protein_id": "ENSP00000552576.1",
          "transcript_support_level": null,
          "aa_start": 442,
          "aa_end": null,
          "aa_length": 596,
          "cds_start": 1324,
          "cds_end": null,
          "cds_length": 1791,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000882517.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.1312delC",
          "hgvs_p": "p.Leu438fs",
          "transcript": "NM_001374625.1",
          "protein_id": "NP_001361554.1",
          "transcript_support_level": null,
          "aa_start": 438,
          "aa_end": null,
          "aa_length": 592,
          "cds_start": 1312,
          "cds_end": null,
          "cds_length": 1779,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001374625.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.1312delC",
          "hgvs_p": "p.Leu438fs",
          "transcript": "ENST00000882515.1",
          "protein_id": "ENSP00000552574.1",
          "transcript_support_level": null,
          "aa_start": 438,
          "aa_end": null,
          "aa_length": 592,
          "cds_start": 1312,
          "cds_end": null,
          "cds_length": 1779,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000882515.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.1315delC",
          "hgvs_p": "p.Leu439fs",
          "transcript": "ENST00000639857.2",
          "protein_id": "ENSP00000491593.2",
          "transcript_support_level": 5,
          "aa_start": 439,
          "aa_end": null,
          "aa_length": 578,
          "cds_start": 1315,
          "cds_end": null,
          "cds_length": 1737,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000639857.2"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.1213delC",
          "hgvs_p": "p.Leu405fs",
          "transcript": "ENST00000882516.1",
          "protein_id": "ENSP00000552575.1",
          "transcript_support_level": null,
          "aa_start": 405,
          "aa_end": null,
          "aa_length": 559,
          "cds_start": 1213,
          "cds_end": null,
          "cds_length": 1680,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000882516.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.1204delC",
          "hgvs_p": "p.Leu402fs",
          "transcript": "ENST00000914890.1",
          "protein_id": "ENSP00000584949.1",
          "transcript_support_level": null,
          "aa_start": 402,
          "aa_end": null,
          "aa_length": 556,
          "cds_start": 1204,
          "cds_end": null,
          "cds_length": 1671,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000914890.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.1201delC",
          "hgvs_p": "p.Leu401fs",
          "transcript": "ENST00000687906.1",
          "protein_id": "ENSP00000509536.1",
          "transcript_support_level": null,
          "aa_start": 401,
          "aa_end": null,
          "aa_length": 555,
          "cds_start": 1201,
          "cds_end": null,
          "cds_length": 1668,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000687906.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.1198delC",
          "hgvs_p": "p.Leu400fs",
          "transcript": "ENST00000971611.1",
          "protein_id": "ENSP00000641670.1",
          "transcript_support_level": null,
          "aa_start": 400,
          "aa_end": null,
          "aa_length": 554,
          "cds_start": 1198,
          "cds_end": null,
          "cds_length": 1665,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000971611.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.1192delC",
          "hgvs_p": "p.Leu398fs",
          "transcript": "ENST00000882518.1",
          "protein_id": "ENSP00000552577.1",
          "transcript_support_level": null,
          "aa_start": 398,
          "aa_end": null,
          "aa_length": 552,
          "cds_start": 1192,
          "cds_end": null,
          "cds_length": 1659,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000882518.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.997delC",
          "hgvs_p": "p.Leu333fs",
          "transcript": "ENST00000971614.1",
          "protein_id": "ENSP00000641673.1",
          "transcript_support_level": null,
          "aa_start": 333,
          "aa_end": null,
          "aa_length": 487,
          "cds_start": 997,
          "cds_end": null,
          "cds_length": 1464,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000971614.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.1315delC",
          "hgvs_p": "p.Leu439fs",
          "transcript": "NM_080601.3",
          "protein_id": "NP_542168.1",
          "transcript_support_level": null,
          "aa_start": 439,
          "aa_end": null,
          "aa_length": 460,
          "cds_start": 1315,
          "cds_end": null,
          "cds_length": 1383,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_080601.3"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.565delC",
          "hgvs_p": "p.Leu189fs",
          "transcript": "ENST00000971612.1",
          "protein_id": "ENSP00000641671.1",
          "transcript_support_level": null,
          "aa_start": 189,
          "aa_end": null,
          "aa_length": 343,
          "cds_start": 565,
          "cds_end": null,
          "cds_length": 1032,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000971612.1"
        },
        {
          "aa_ref": "L",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PTPN11",
          "gene_hgnc_id": 9644,
          "hgvs_c": "c.523delC",
          "hgvs_p": "p.Leu175fs",
          "transcript": "ENST00000971613.1",
          "protein_id": "ENSP00000641672.1",
          "transcript_support_level": null,
          "aa_start": 175,
          "aa_end": null,
          "aa_length": 329,
          "cds_start": 523,
          "cds_end": null,
          "cds_length": 990,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000971613.1"
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        {
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      "computational_score_selected": null,
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      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
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      "phylop100way_score": 0.673,
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      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1,PM2,PP5",
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            "PP5"
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          "transcript": "NM_001330437.2",
          "gene_symbol": "PTPN11",
          "hgnc_id": 9644,
          "effects": [
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          "hgvs_p": "p.Leu443fs"
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      "clinvar_disease": "Metachondromatosis",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "no assertion criteria provided",
      "clinvar_submissions_summary": "null",
      "phenotype_combined": "Metachondromatosis",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}
For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.