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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: 11-6616033-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=6616033&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 6616033,
      "ref": "G",
      "alt": "A",
      "effect": "stop_gained",
      "transcript": "ENST00000299427.12",
      "consequences": [
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "c.1117C>T",
          "hgvs_p": "p.Gln373*",
          "transcript": "NM_000391.4",
          "protein_id": "NP_000382.3",
          "transcript_support_level": null,
          "aa_start": 373,
          "aa_end": null,
          "aa_length": 563,
          "cds_start": 1117,
          "cds_end": null,
          "cds_length": 1692,
          "cdna_start": 1139,
          "cdna_end": null,
          "cdna_length": 3492,
          "mane_select": "ENST00000299427.12",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "c.1117C>T",
          "hgvs_p": "p.Gln373*",
          "transcript": "ENST00000299427.12",
          "protein_id": "ENSP00000299427.6",
          "transcript_support_level": 1,
          "aa_start": 373,
          "aa_end": null,
          "aa_length": 563,
          "cds_start": 1117,
          "cds_end": null,
          "cds_length": 1692,
          "cdna_start": 1139,
          "cdna_end": null,
          "cdna_length": 3492,
          "mane_select": "NM_000391.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "c.388C>T",
          "hgvs_p": "p.Gln130*",
          "transcript": "ENST00000533371.6",
          "protein_id": "ENSP00000437066.1",
          "transcript_support_level": 1,
          "aa_start": 130,
          "aa_end": null,
          "aa_length": 320,
          "cds_start": 388,
          "cds_end": null,
          "cds_length": 963,
          "cdna_start": 1229,
          "cdna_end": null,
          "cdna_length": 3578,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "c.1003C>T",
          "hgvs_p": "p.Gln335*",
          "transcript": "ENST00000682424.1",
          "protein_id": "ENSP00000507321.1",
          "transcript_support_level": null,
          "aa_start": 335,
          "aa_end": null,
          "aa_length": 525,
          "cds_start": 1003,
          "cds_end": null,
          "cds_length": 1578,
          "cdna_start": 1005,
          "cdna_end": null,
          "cdna_length": 3353,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "c.928C>T",
          "hgvs_p": "p.Gln310*",
          "transcript": "ENST00000644218.1",
          "protein_id": "ENSP00000493574.1",
          "transcript_support_level": null,
          "aa_start": 310,
          "aa_end": null,
          "aa_length": 500,
          "cds_start": 928,
          "cds_end": null,
          "cds_length": 1503,
          "cdna_start": 957,
          "cdna_end": null,
          "cdna_length": 3292,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "c.838C>T",
          "hgvs_p": "p.Gln280*",
          "transcript": "ENST00000644810.1",
          "protein_id": "ENSP00000495895.1",
          "transcript_support_level": null,
          "aa_start": 280,
          "aa_end": null,
          "aa_length": 470,
          "cds_start": 838,
          "cds_end": null,
          "cds_length": 1413,
          "cdna_start": 851,
          "cdna_end": null,
          "cdna_length": 3190,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "c.625C>T",
          "hgvs_p": "p.Gln209*",
          "transcript": "ENST00000643516.1",
          "protein_id": "ENSP00000496372.1",
          "transcript_support_level": null,
          "aa_start": 209,
          "aa_end": null,
          "aa_length": 399,
          "cds_start": 625,
          "cds_end": null,
          "cds_length": 1200,
          "cdna_start": 626,
          "cdna_end": null,
          "cdna_length": 2915,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "c.388C>T",
          "hgvs_p": "p.Gln130*",
          "transcript": "ENST00000642892.1",
          "protein_id": "ENSP00000494165.1",
          "transcript_support_level": null,
          "aa_start": 130,
          "aa_end": null,
          "aa_length": 320,
          "cds_start": 388,
          "cds_end": null,
          "cds_length": 963,
          "cdna_start": 1133,
          "cdna_end": null,
          "cdna_length": 3470,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "c.388C>T",
          "hgvs_p": "p.Gln130*",
          "transcript": "ENST00000645620.1",
          "protein_id": "ENSP00000493657.1",
          "transcript_support_level": null,
          "aa_start": 130,
          "aa_end": null,
          "aa_length": 320,
          "cds_start": 388,
          "cds_end": null,
          "cds_length": 963,
          "cdna_start": 1144,
          "cdna_end": null,
          "cdna_length": 3464,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "c.388C>T",
          "hgvs_p": "p.Gln130*",
          "transcript": "ENST00000647152.1",
          "protein_id": "ENSP00000495893.1",
          "transcript_support_level": null,
          "aa_start": 130,
          "aa_end": null,
          "aa_length": 320,
          "cds_start": 388,
          "cds_end": null,
          "cds_length": 963,
          "cdna_start": 1102,
          "cdna_end": null,
          "cdna_length": 3414,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "c.352C>T",
          "hgvs_p": "p.Gln118*",
          "transcript": "ENST00000436873.7",
          "protein_id": "ENSP00000398136.3",
          "transcript_support_level": 4,
          "aa_start": 118,
          "aa_end": null,
          "aa_length": 168,
          "cds_start": 352,
          "cds_end": null,
          "cds_length": 509,
          "cdna_start": 354,
          "cdna_end": null,
          "cdna_length": 511,
          "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": 1,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "n.237C>T",
          "hgvs_p": null,
          "transcript": "ENST00000524924.2",
          "protein_id": null,
          "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": 757,
          "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": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000285338",
          "gene_hgnc_id": null,
          "hgvs_c": "n.322C>T",
          "hgvs_p": null,
          "transcript": "ENST00000532191.2",
          "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": 1349,
          "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": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "n.205C>T",
          "hgvs_p": null,
          "transcript": "ENST00000643342.1",
          "protein_id": "ENSP00000494324.1",
          "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": 2007,
          "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": 8,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "n.*857C>T",
          "hgvs_p": null,
          "transcript": "ENST00000643439.1",
          "protein_id": "ENSP00000495849.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3288,
          "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": 8,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "n.1303C>T",
          "hgvs_p": null,
          "transcript": "ENST00000643479.1",
          "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": 3640,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "n.*570C>T",
          "hgvs_p": null,
          "transcript": "ENST00000644683.1",
          "protein_id": "ENSP00000494085.1",
          "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": 3333,
          "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": 8,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "n.1293C>T",
          "hgvs_p": null,
          "transcript": "ENST00000644831.1",
          "protein_id": null,
          "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,
          "cdna_end": null,
          "cdna_length": 3620,
          "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": 8,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "n.388C>T",
          "hgvs_p": null,
          "transcript": "ENST00000644933.1",
          "protein_id": "ENSP00000496133.1",
          "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": 3507,
          "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": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "n.199C>T",
          "hgvs_p": null,
          "transcript": "ENST00000645285.1",
          "protein_id": "ENSP00000495058.1",
          "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": 3306,
          "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": 5,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "TPP1",
          "gene_hgnc_id": 2073,
          "hgvs_c": "n.1880C>T",
          "hgvs_p": null,
          "transcript": "ENST00000645331.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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        {
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      ],
      "gene_symbol": "TPP1",
      "gene_hgnc_id": 2073,
      "dbsnp": "rs112812685",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.49000000953674316,
      "computational_prediction_selected": "Pathogenic",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.009999999776482582,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": 0.49,
      "bayesdelnoaf_prediction": "Pathogenic",
      "phylop100way_score": 1.264,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.01,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
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      "acmg_score": 12,
      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1,PM2,PP5_Moderate",
      "acmg_by_gene": [
        {
          "score": 12,
          "benign_score": 0,
          "pathogenic_score": 12,
          "criteria": [
            "PVS1",
            "PM2",
            "PP5_Moderate"
          ],
          "verdict": "Pathogenic",
          "transcript": "ENST00000299427.12",
          "gene_symbol": "TPP1",
          "hgnc_id": 2073,
          "effects": [
            "stop_gained"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.1117C>T",
          "hgvs_p": "p.Gln373*"
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        {
          "score": 8,
          "benign_score": 0,
          "pathogenic_score": 8,
          "criteria": [
            "PM2",
            "PP3_Strong",
            "PP5_Moderate"
          ],
          "verdict": "Likely_pathogenic",
          "transcript": "ENST00000532191.2",
          "gene_symbol": "ENSG00000285338",
          "hgnc_id": null,
          "effects": [
            "non_coding_transcript_exon_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.322C>T",
          "hgvs_p": null
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      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "P:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}