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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: 11-72302312-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=72302312&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "11",
      "pos": 72302312,
      "ref": "G",
      "alt": "C",
      "effect": "missense_variant",
      "transcript": "ENST00000538039.6",
      "consequences": [
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "c.1249C>G",
          "hgvs_p": "p.Arg417Gly",
          "transcript": "NM_030813.6",
          "protein_id": "NP_110440.1",
          "transcript_support_level": null,
          "aa_start": 417,
          "aa_end": null,
          "aa_length": 707,
          "cds_start": 1249,
          "cds_end": null,
          "cds_length": 2124,
          "cdna_start": 1306,
          "cdna_end": null,
          "cdna_length": 10053,
          "mane_select": null,
          "mane_plus": "ENST00000294053.9",
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "c.1249C>G",
          "hgvs_p": "p.Arg417Gly",
          "transcript": "ENST00000294053.9",
          "protein_id": "ENSP00000294053.3",
          "transcript_support_level": 1,
          "aa_start": 417,
          "aa_end": null,
          "aa_length": 707,
          "cds_start": 1249,
          "cds_end": null,
          "cds_length": 2124,
          "cdna_start": 1306,
          "cdna_end": null,
          "cdna_length": 10053,
          "mane_select": null,
          "mane_plus": "NM_030813.6",
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "c.1159C>G",
          "hgvs_p": "p.Arg387Gly",
          "transcript": "NM_001258392.3",
          "protein_id": "NP_001245321.1",
          "transcript_support_level": null,
          "aa_start": 387,
          "aa_end": null,
          "aa_length": 677,
          "cds_start": 1159,
          "cds_end": null,
          "cds_length": 2034,
          "cdna_start": 1216,
          "cdna_end": null,
          "cdna_length": 9963,
          "mane_select": "ENST00000538039.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "c.1159C>G",
          "hgvs_p": "p.Arg387Gly",
          "transcript": "ENST00000538039.6",
          "protein_id": "ENSP00000441518.1",
          "transcript_support_level": 2,
          "aa_start": 387,
          "aa_end": null,
          "aa_length": 677,
          "cds_start": 1159,
          "cds_end": null,
          "cds_length": 2034,
          "cdna_start": 1216,
          "cdna_end": null,
          "cdna_length": 9963,
          "mane_select": "NM_001258392.3",
          "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": 3,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "n.176C>G",
          "hgvs_p": null,
          "transcript": "ENST00000538021.5",
          "protein_id": "ENSP00000445180.2",
          "transcript_support_level": 1,
          "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": 1108,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "c.1114C>G",
          "hgvs_p": "p.Arg372Gly",
          "transcript": "NM_001258394.3",
          "protein_id": "NP_001245323.1",
          "transcript_support_level": null,
          "aa_start": 372,
          "aa_end": null,
          "aa_length": 662,
          "cds_start": 1114,
          "cds_end": null,
          "cds_length": 1989,
          "cdna_start": 1413,
          "cdna_end": null,
          "cdna_length": 10160,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "c.1072C>G",
          "hgvs_p": "p.Arg358Gly",
          "transcript": "NM_001258393.3",
          "protein_id": "NP_001245322.1",
          "transcript_support_level": null,
          "aa_start": 358,
          "aa_end": null,
          "aa_length": 648,
          "cds_start": 1072,
          "cds_end": null,
          "cds_length": 1947,
          "cdna_start": 1129,
          "cdna_end": null,
          "cdna_length": 9876,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "c.1072C>G",
          "hgvs_p": "p.Arg358Gly",
          "transcript": "ENST00000340729.9",
          "protein_id": "ENSP00000340385.5",
          "transcript_support_level": 2,
          "aa_start": 358,
          "aa_end": null,
          "aa_length": 648,
          "cds_start": 1072,
          "cds_end": null,
          "cds_length": 1947,
          "cdna_start": 1132,
          "cdna_end": null,
          "cdna_length": 2071,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "c.646C>G",
          "hgvs_p": "p.Arg216Gly",
          "transcript": "ENST00000642288.1",
          "protein_id": "ENSP00000495167.1",
          "transcript_support_level": null,
          "aa_start": 216,
          "aa_end": null,
          "aa_length": 381,
          "cds_start": 646,
          "cds_end": null,
          "cds_length": 1146,
          "cdna_start": 921,
          "cdna_end": null,
          "cdna_length": 1421,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "c.1162C>G",
          "hgvs_p": "p.Arg388Gly",
          "transcript": "XM_005274320.2",
          "protein_id": "XP_005274377.1",
          "transcript_support_level": null,
          "aa_start": 388,
          "aa_end": null,
          "aa_length": 678,
          "cds_start": 1162,
          "cds_end": null,
          "cds_length": 2037,
          "cdna_start": 1219,
          "cdna_end": null,
          "cdna_length": 9966,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "c.1024C>G",
          "hgvs_p": "p.Arg342Gly",
          "transcript": "XM_047427655.1",
          "protein_id": "XP_047283611.1",
          "transcript_support_level": null,
          "aa_start": 342,
          "aa_end": null,
          "aa_length": 632,
          "cds_start": 1024,
          "cds_end": null,
          "cds_length": 1899,
          "cdna_start": 1323,
          "cdna_end": null,
          "cdna_length": 10070,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "R",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "c.736C>G",
          "hgvs_p": "p.Arg246Gly",
          "transcript": "XM_047427656.1",
          "protein_id": "XP_047283612.1",
          "transcript_support_level": null,
          "aa_start": 246,
          "aa_end": null,
          "aa_length": 536,
          "cds_start": 736,
          "cds_end": null,
          "cds_length": 1611,
          "cdna_start": 1515,
          "cdna_end": null,
          "cdna_length": 10262,
          "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": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "n.*584C>G",
          "hgvs_p": null,
          "transcript": "ENST00000535477.6",
          "protein_id": "ENSP00000440423.2",
          "transcript_support_level": 5,
          "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": 2133,
          "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": 12,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "n.*849C>G",
          "hgvs_p": null,
          "transcript": "ENST00000535990.6",
          "protein_id": "ENSP00000443822.2",
          "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": 2501,
          "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": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "n.582C>G",
          "hgvs_p": null,
          "transcript": "ENST00000544382.5",
          "protein_id": null,
          "transcript_support_level": 5,
          "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": 982,
          "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": 1,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000255843",
          "gene_hgnc_id": null,
          "hgvs_c": "n.174G>C",
          "hgvs_p": null,
          "transcript": "ENST00000546065.1",
          "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": 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": 8,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "n.*241C>G",
          "hgvs_p": null,
          "transcript": "ENST00000642187.1",
          "protein_id": "ENSP00000494594.1",
          "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": 1609,
          "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": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "n.577C>G",
          "hgvs_p": null,
          "transcript": "ENST00000645105.1",
          "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": 1522,
          "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": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "n.503C>G",
          "hgvs_p": null,
          "transcript": "ENST00000645650.1",
          "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": 507,
          "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": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "n.337C>G",
          "hgvs_p": null,
          "transcript": "ENST00000646359.1",
          "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": 1269,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CLPB",
          "gene_hgnc_id": 30664,
          "hgvs_c": "n.1230C>G",
          "hgvs_p": null,
          "transcript": "ENST00000695924.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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      "gnomad_exomes_af": 6.84086e-7,
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      "bayesdelnoaf_score": -0.17,
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      "phylop100way_score": 5.26,
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      "acmg_score": 2,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2",
      "acmg_by_gene": [
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          "verdict": "Uncertain_significance",
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        {
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          "verdict": "Uncertain_significance",
          "transcript": "ENST00000546065.1",
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          "effects": [
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          "inheritance_mode": "",
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        },
        {
          "score": 2,
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          "verdict": "Uncertain_significance",
          "transcript": "XR_007062766.1",
          "gene_symbol": "LOC124902708",
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          "effects": [
            "non_coding_transcript_exon_variant"
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          "inheritance_mode": "",
          "hgvs_c": "n.1894G>C",
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      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}