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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: 12-32582122-A-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=32582122&ref=A&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "12",
      "pos": 32582122,
      "ref": "A",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "ENST00000534526.7",
      "consequences": [
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "c.666A>T",
          "hgvs_p": "p.Ala222Ala",
          "transcript": "NM_001370298.3",
          "protein_id": "NP_001357227.2",
          "transcript_support_level": null,
          "aa_start": 222,
          "aa_end": null,
          "aa_length": 903,
          "cds_start": 666,
          "cds_end": null,
          "cds_length": 2712,
          "cdna_start": 902,
          "cdna_end": null,
          "cdna_length": 8465,
          "mane_select": "ENST00000534526.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "c.666A>T",
          "hgvs_p": "p.Ala222Ala",
          "transcript": "ENST00000534526.7",
          "protein_id": "ENSP00000449273.1",
          "transcript_support_level": 5,
          "aa_start": 222,
          "aa_end": null,
          "aa_length": 903,
          "cds_start": 666,
          "cds_end": null,
          "cds_length": 2712,
          "cdna_start": 902,
          "cdna_end": null,
          "cdna_length": 8465,
          "mane_select": "NM_001370298.3",
          "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": 4,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "n.255A>T",
          "hgvs_p": null,
          "transcript": "ENST00000395740.5",
          "protein_id": "ENSP00000379089.1",
          "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": 2691,
          "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": 3,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "n.606A>T",
          "hgvs_p": null,
          "transcript": "ENST00000494275.5",
          "protein_id": null,
          "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": 1439,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "c.666A>T",
          "hgvs_p": "p.Ala222Ala",
          "transcript": "NM_001384126.1",
          "protein_id": "NP_001371055.1",
          "transcript_support_level": null,
          "aa_start": 222,
          "aa_end": null,
          "aa_length": 887,
          "cds_start": 666,
          "cds_end": null,
          "cds_length": 2664,
          "cdna_start": 902,
          "cdna_end": null,
          "cdna_length": 4325,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "c.510A>T",
          "hgvs_p": "p.Ala170Ala",
          "transcript": "NM_001304481.2",
          "protein_id": "NP_001291410.1",
          "transcript_support_level": null,
          "aa_start": 170,
          "aa_end": null,
          "aa_length": 851,
          "cds_start": 510,
          "cds_end": null,
          "cds_length": 2556,
          "cdna_start": 672,
          "cdna_end": null,
          "cdna_length": 8235,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "c.510A>T",
          "hgvs_p": "p.Ala170Ala",
          "transcript": "ENST00000531134.7",
          "protein_id": "ENSP00000431323.1",
          "transcript_support_level": 2,
          "aa_start": 170,
          "aa_end": null,
          "aa_length": 851,
          "cds_start": 510,
          "cds_end": null,
          "cds_length": 2556,
          "cdna_start": 672,
          "cdna_end": null,
          "cdna_length": 2924,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "c.255A>T",
          "hgvs_p": "p.Ala85Ala",
          "transcript": "NM_001385118.1",
          "protein_id": "NP_001372047.1",
          "transcript_support_level": null,
          "aa_start": 85,
          "aa_end": null,
          "aa_length": 766,
          "cds_start": 255,
          "cds_end": null,
          "cds_length": 2301,
          "cdna_start": 677,
          "cdna_end": null,
          "cdna_length": 8240,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "c.255A>T",
          "hgvs_p": "p.Ala85Ala",
          "transcript": "NM_139241.3",
          "protein_id": "NP_640334.2",
          "transcript_support_level": null,
          "aa_start": 85,
          "aa_end": null,
          "aa_length": 766,
          "cds_start": 255,
          "cds_end": null,
          "cds_length": 2301,
          "cdna_start": 796,
          "cdna_end": null,
          "cdna_length": 8359,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "c.255A>T",
          "hgvs_p": "p.Ala85Ala",
          "transcript": "ENST00000427716.7",
          "protein_id": "ENSP00000394487.2",
          "transcript_support_level": 2,
          "aa_start": 85,
          "aa_end": null,
          "aa_length": 766,
          "cds_start": 255,
          "cds_end": null,
          "cds_length": 2301,
          "cdna_start": 804,
          "cdna_end": null,
          "cdna_length": 7194,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "c.255A>T",
          "hgvs_p": "p.Ala85Ala",
          "transcript": "ENST00000525053.6",
          "protein_id": "ENSP00000433666.2",
          "transcript_support_level": 2,
          "aa_start": 85,
          "aa_end": null,
          "aa_length": 766,
          "cds_start": 255,
          "cds_end": null,
          "cds_length": 2301,
          "cdna_start": 675,
          "cdna_end": null,
          "cdna_length": 2925,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "c.255A>T",
          "hgvs_p": "p.Ala85Ala",
          "transcript": "ENST00000583694.2",
          "protein_id": "ENSP00000462623.2",
          "transcript_support_level": 3,
          "aa_start": 85,
          "aa_end": null,
          "aa_length": 766,
          "cds_start": 255,
          "cds_end": null,
          "cds_length": 2301,
          "cdna_start": 679,
          "cdna_end": null,
          "cdna_length": 2931,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "c.255A>T",
          "hgvs_p": "p.Ala85Ala",
          "transcript": "NM_001384127.1",
          "protein_id": "NP_001371056.1",
          "transcript_support_level": null,
          "aa_start": 85,
          "aa_end": null,
          "aa_length": 750,
          "cds_start": 255,
          "cds_end": null,
          "cds_length": 2253,
          "cdna_start": 676,
          "cdna_end": null,
          "cdna_length": 4099,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "c.255A>T",
          "hgvs_p": "p.Ala85Ala",
          "transcript": "NM_001384128.1",
          "protein_id": "NP_001371057.1",
          "transcript_support_level": null,
          "aa_start": 85,
          "aa_end": null,
          "aa_length": 750,
          "cds_start": 255,
          "cds_end": null,
          "cds_length": 2253,
          "cdna_start": 677,
          "cdna_end": null,
          "cdna_length": 4100,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "c.255A>T",
          "hgvs_p": "p.Ala85Ala",
          "transcript": "NM_001384131.1",
          "protein_id": "NP_001371060.1",
          "transcript_support_level": null,
          "aa_start": 85,
          "aa_end": null,
          "aa_length": 207,
          "cds_start": 255,
          "cds_end": null,
          "cds_length": 624,
          "cdna_start": 676,
          "cdna_end": null,
          "cdna_length": 1509,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "c.255A>T",
          "hgvs_p": "p.Ala85Ala",
          "transcript": "NM_001384132.1",
          "protein_id": "NP_001371061.1",
          "transcript_support_level": null,
          "aa_start": 85,
          "aa_end": null,
          "aa_length": 207,
          "cds_start": 255,
          "cds_end": null,
          "cds_length": 624,
          "cdna_start": 677,
          "cdna_end": null,
          "cdna_length": 1510,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "c.255A>T",
          "hgvs_p": "p.Ala85Ala",
          "transcript": "ENST00000472289.5",
          "protein_id": "ENSP00000434356.1",
          "transcript_support_level": 2,
          "aa_start": 85,
          "aa_end": null,
          "aa_length": 207,
          "cds_start": 255,
          "cds_end": null,
          "cds_length": 624,
          "cdna_start": 796,
          "cdna_end": null,
          "cdna_length": 1629,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "c.723A>T",
          "hgvs_p": "p.Ala241Ala",
          "transcript": "XM_047428291.1",
          "protein_id": "XP_047284247.1",
          "transcript_support_level": null,
          "aa_start": 241,
          "aa_end": null,
          "aa_length": 922,
          "cds_start": 723,
          "cds_end": null,
          "cds_length": 2769,
          "cdna_start": 752,
          "cdna_end": null,
          "cdna_length": 8315,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "c.681A>T",
          "hgvs_p": "p.Ala227Ala",
          "transcript": "XM_047428292.1",
          "protein_id": "XP_047284248.1",
          "transcript_support_level": null,
          "aa_start": 227,
          "aa_end": null,
          "aa_length": 908,
          "cds_start": 681,
          "cds_end": null,
          "cds_length": 2727,
          "cdna_start": 876,
          "cdna_end": null,
          "cdna_length": 8439,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "A",
          "aa_alt": "A",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "c.255A>T",
          "hgvs_p": "p.Ala85Ala",
          "transcript": "XM_047428293.1",
          "protein_id": "XP_047284249.1",
          "transcript_support_level": null,
          "aa_start": 85,
          "aa_end": null,
          "aa_length": 766,
          "cds_start": 255,
          "cds_end": null,
          "cds_length": 2301,
          "cdna_start": 543,
          "cdna_end": null,
          "cdna_length": 8106,
          "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": 4,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "FGD4",
          "gene_hgnc_id": 19125,
          "hgvs_c": "n.255A>T",
          "hgvs_p": null,
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      "computational_source_selected": "BayesDel_noAF",
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      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
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      "acmg_score": -14,
      "acmg_classification": "Benign",
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      "acmg_by_gene": [
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      "clinvar_classification": "Conflicting classifications of pathogenicity",
      "clinvar_review_status": "criteria provided, conflicting classifications",
      "clinvar_submissions_summary": "US:1 LB:7",
      "phenotype_combined": "Charcot-Marie-Tooth disease type 4|not specified|Charcot-Marie-Tooth disease|not provided|Charcot-Marie-Tooth disease type 4H|Inborn genetic diseases",
      "pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
      "custom_annotations": null
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  ],
  "message": null
}