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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: X-38269772-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=38269772&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "X",
      "pos": 38269772,
      "ref": "G",
      "alt": "A",
      "effect": "intron_variant",
      "transcript": "ENST00000465127.1",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000250349",
          "gene_hgnc_id": null,
          "hgvs_c": "c.172-396349G>A",
          "hgvs_p": null,
          "transcript": "ENST00000465127.1",
          "protein_id": "ENSP00000417050.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 279,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 840,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 954,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "c.2917C>T",
          "hgvs_p": "p.Pro973Ser",
          "transcript": "ENST00000339363.7",
          "protein_id": "ENSP00000343671.3",
          "transcript_support_level": 5,
          "aa_start": 973,
          "aa_end": null,
          "aa_length": 1020,
          "cds_start": 2917,
          "cds_end": null,
          "cds_length": 3063,
          "cdna_start": 3085,
          "cdna_end": null,
          "cdna_length": 3686,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "c.2302C>T",
          "hgvs_p": "p.Pro768Ser",
          "transcript": "NM_000328.3",
          "protein_id": "NP_000319.1",
          "transcript_support_level": null,
          "aa_start": 768,
          "aa_end": null,
          "aa_length": 815,
          "cds_start": 2302,
          "cds_end": null,
          "cds_length": 2448,
          "cdna_start": 2444,
          "cdna_end": null,
          "cdna_length": 3053,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "c.2302C>T",
          "hgvs_p": "p.Pro768Ser",
          "transcript": "ENST00000642395.2",
          "protein_id": "ENSP00000493468.2",
          "transcript_support_level": null,
          "aa_start": 768,
          "aa_end": null,
          "aa_length": 815,
          "cds_start": 2302,
          "cds_end": null,
          "cds_length": 2448,
          "cdna_start": 2444,
          "cdna_end": null,
          "cdna_length": 3053,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "c.2299C>T",
          "hgvs_p": "p.Pro767Ser",
          "transcript": "NM_001367245.1",
          "protein_id": "NP_001354174.1",
          "transcript_support_level": null,
          "aa_start": 767,
          "aa_end": null,
          "aa_length": 814,
          "cds_start": 2299,
          "cds_end": null,
          "cds_length": 2445,
          "cdna_start": 2441,
          "cdna_end": null,
          "cdna_length": 3050,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "c.2116C>T",
          "hgvs_p": "p.Pro706Ser",
          "transcript": "NM_001367246.1",
          "protein_id": "NP_001354175.1",
          "transcript_support_level": null,
          "aa_start": 706,
          "aa_end": null,
          "aa_length": 753,
          "cds_start": 2116,
          "cds_end": null,
          "cds_length": 2262,
          "cdna_start": 2258,
          "cdna_end": null,
          "cdna_length": 2867,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "c.2116C>T",
          "hgvs_p": "p.Pro706Ser",
          "transcript": "ENST00000644337.1",
          "protein_id": "ENSP00000494557.1",
          "transcript_support_level": null,
          "aa_start": 706,
          "aa_end": null,
          "aa_length": 753,
          "cds_start": 2116,
          "cds_end": null,
          "cds_length": 2262,
          "cdna_start": 2284,
          "cdna_end": null,
          "cdna_length": 2559,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "c.1999C>T",
          "hgvs_p": "p.Pro667Ser",
          "transcript": "NM_001367248.1",
          "protein_id": "NP_001354177.1",
          "transcript_support_level": null,
          "aa_start": 667,
          "aa_end": null,
          "aa_length": 714,
          "cds_start": 1999,
          "cds_end": null,
          "cds_length": 2145,
          "cdna_start": 2037,
          "cdna_end": null,
          "cdna_length": 2646,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "c.1969C>T",
          "hgvs_p": "p.Pro657Ser",
          "transcript": "NM_001367247.1",
          "protein_id": "NP_001354176.1",
          "transcript_support_level": null,
          "aa_start": 657,
          "aa_end": null,
          "aa_length": 704,
          "cds_start": 1969,
          "cds_end": null,
          "cds_length": 2115,
          "cdna_start": 2111,
          "cdna_end": null,
          "cdna_length": 2720,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "c.1966C>T",
          "hgvs_p": "p.Pro656Ser",
          "transcript": "NM_001367249.1",
          "protein_id": "NP_001354178.1",
          "transcript_support_level": null,
          "aa_start": 656,
          "aa_end": null,
          "aa_length": 703,
          "cds_start": 1966,
          "cds_end": null,
          "cds_length": 2112,
          "cdna_start": 2108,
          "cdna_end": null,
          "cdna_length": 2717,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "c.1966C>T",
          "hgvs_p": "p.Pro656Ser",
          "transcript": "NM_001367250.1",
          "protein_id": "NP_001354179.1",
          "transcript_support_level": null,
          "aa_start": 656,
          "aa_end": null,
          "aa_length": 703,
          "cds_start": 1966,
          "cds_end": null,
          "cds_length": 2112,
          "cdna_start": 2108,
          "cdna_end": null,
          "cdna_length": 2717,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "c.1783C>T",
          "hgvs_p": "p.Pro595Ser",
          "transcript": "NM_001367251.1",
          "protein_id": "NP_001354180.1",
          "transcript_support_level": null,
          "aa_start": 595,
          "aa_end": null,
          "aa_length": 642,
          "cds_start": 1783,
          "cds_end": null,
          "cds_length": 1929,
          "cdna_start": 1925,
          "cdna_end": null,
          "cdna_length": 2534,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "c.1783C>T",
          "hgvs_p": "p.Pro595Ser",
          "transcript": "ENST00000644238.1",
          "protein_id": "ENSP00000496728.1",
          "transcript_support_level": null,
          "aa_start": 595,
          "aa_end": null,
          "aa_length": 642,
          "cds_start": 1783,
          "cds_end": null,
          "cds_length": 1929,
          "cdna_start": 1931,
          "cdna_end": null,
          "cdna_length": 2301,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "c.2917C>T",
          "hgvs_p": "p.Pro973Ser",
          "transcript": "XM_047442329.1",
          "protein_id": "XP_047298285.1",
          "transcript_support_level": null,
          "aa_start": 973,
          "aa_end": null,
          "aa_length": 1020,
          "cds_start": 2917,
          "cds_end": null,
          "cds_length": 3063,
          "cdna_start": 3059,
          "cdna_end": null,
          "cdna_length": 3668,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "c.2914C>T",
          "hgvs_p": "p.Pro972Ser",
          "transcript": "XM_047442330.1",
          "protein_id": "XP_047298286.1",
          "transcript_support_level": null,
          "aa_start": 972,
          "aa_end": null,
          "aa_length": 1019,
          "cds_start": 2914,
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          "cds_length": 3060,
          "cdna_start": 3056,
          "cdna_end": null,
          "cdna_length": 3665,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "c.1522C>T",
          "hgvs_p": "p.Pro508Ser",
          "transcript": "XM_047442331.1",
          "protein_id": "XP_047298287.1",
          "transcript_support_level": null,
          "aa_start": 508,
          "aa_end": null,
          "aa_length": 555,
          "cds_start": 1522,
          "cds_end": null,
          "cds_length": 1668,
          "cdna_start": 1668,
          "cdna_end": null,
          "cdna_length": 2277,
          "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": 16,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "n.*434C>T",
          "hgvs_p": null,
          "transcript": "ENST00000474584.5",
          "protein_id": "ENSP00000418926.1",
          "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": 2268,
          "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": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "n.618C>T",
          "hgvs_p": null,
          "transcript": "ENST00000476559.2",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1047,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "n.*400C>T",
          "hgvs_p": null,
          "transcript": "ENST00000482855.5",
          "protein_id": "ENSP00000419276.1",
          "transcript_support_level": 2,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2819,
          "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": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "n.2502C>T",
          "hgvs_p": null,
          "transcript": "ENST00000642170.1",
          "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": 2872,
          "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": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "RPGR",
          "gene_hgnc_id": 10295,
          "hgvs_c": "n.*226C>T",
          "hgvs_p": null,
          "transcript": "ENST00000642739.1",
          "protein_id": "ENSP00000493596.1",
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          "verdict": "Uncertain_significance",
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
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  "message": null
}