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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: 2-208326119-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=208326119&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 208326119,
      "ref": "A",
      "alt": "G",
      "effect": "missense_variant",
      "transcript": "ENST00000264380.9",
      "consequences": [
        {
          "aa_ref": "K",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3308A>G",
          "hgvs_p": "p.Lys1103Arg",
          "transcript": "NM_015040.4",
          "protein_id": "NP_055855.2",
          "transcript_support_level": null,
          "aa_start": 1103,
          "aa_end": null,
          "aa_length": 2098,
          "cds_start": 3308,
          "cds_end": null,
          "cds_length": 6297,
          "cdna_start": 3478,
          "cdna_end": null,
          "cdna_length": 9908,
          "mane_select": "ENST00000264380.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "R",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3308A>G",
          "hgvs_p": "p.Lys1103Arg",
          "transcript": "ENST00000264380.9",
          "protein_id": "ENSP00000264380.4",
          "transcript_support_level": 1,
          "aa_start": 1103,
          "aa_end": null,
          "aa_length": 2098,
          "cds_start": 3308,
          "cds_end": null,
          "cds_length": 6297,
          "cdna_start": 3478,
          "cdna_end": null,
          "cdna_length": 9908,
          "mane_select": "NM_015040.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3140A>G",
          "hgvs_p": "p.Lys1047Arg",
          "transcript": "ENST00000452564.1",
          "protein_id": "ENSP00000405736.1",
          "transcript_support_level": 2,
          "aa_start": 1047,
          "aa_end": null,
          "aa_length": 1383,
          "cds_start": 3140,
          "cds_end": null,
          "cds_length": 4152,
          "cdna_start": 3202,
          "cdna_end": null,
          "cdna_length": 4214,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 43,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3344A>G",
          "hgvs_p": "p.Lys1115Arg",
          "transcript": "XM_011510778.4",
          "protein_id": "XP_011509080.1",
          "transcript_support_level": null,
          "aa_start": 1115,
          "aa_end": null,
          "aa_length": 2110,
          "cds_start": 3344,
          "cds_end": null,
          "cds_length": 6333,
          "cdna_start": 3514,
          "cdna_end": null,
          "cdna_length": 9944,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 43,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3344A>G",
          "hgvs_p": "p.Lys1115Arg",
          "transcript": "XM_011510779.3",
          "protein_id": "XP_011509081.1",
          "transcript_support_level": null,
          "aa_start": 1115,
          "aa_end": null,
          "aa_length": 2110,
          "cds_start": 3344,
          "cds_end": null,
          "cds_length": 6333,
          "cdna_start": 3571,
          "cdna_end": null,
          "cdna_length": 10001,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 43,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3341A>G",
          "hgvs_p": "p.Lys1114Arg",
          "transcript": "XM_011510780.3",
          "protein_id": "XP_011509082.1",
          "transcript_support_level": null,
          "aa_start": 1114,
          "aa_end": null,
          "aa_length": 2109,
          "cds_start": 3341,
          "cds_end": null,
          "cds_length": 6330,
          "cdna_start": 3511,
          "cdna_end": null,
          "cdna_length": 9941,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 43,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3326A>G",
          "hgvs_p": "p.Lys1109Arg",
          "transcript": "XM_011510781.4",
          "protein_id": "XP_011509083.1",
          "transcript_support_level": null,
          "aa_start": 1109,
          "aa_end": null,
          "aa_length": 2104,
          "cds_start": 3326,
          "cds_end": null,
          "cds_length": 6315,
          "cdna_start": 3496,
          "cdna_end": null,
          "cdna_length": 9926,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3308A>G",
          "hgvs_p": "p.Lys1103Arg",
          "transcript": "XM_047443667.1",
          "protein_id": "XP_047299623.1",
          "transcript_support_level": null,
          "aa_start": 1103,
          "aa_end": null,
          "aa_length": 2098,
          "cds_start": 3308,
          "cds_end": null,
          "cds_length": 6297,
          "cdna_start": 3535,
          "cdna_end": null,
          "cdna_length": 9965,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3290A>G",
          "hgvs_p": "p.Lys1097Arg",
          "transcript": "XM_017003568.2",
          "protein_id": "XP_016859057.1",
          "transcript_support_level": null,
          "aa_start": 1097,
          "aa_end": null,
          "aa_length": 2092,
          "cds_start": 3290,
          "cds_end": null,
          "cds_length": 6279,
          "cdna_start": 3460,
          "cdna_end": null,
          "cdna_length": 9890,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3344A>G",
          "hgvs_p": "p.Lys1115Arg",
          "transcript": "XM_011510782.4",
          "protein_id": "XP_011509084.1",
          "transcript_support_level": null,
          "aa_start": 1115,
          "aa_end": null,
          "aa_length": 2055,
          "cds_start": 3344,
          "cds_end": null,
          "cds_length": 6168,
          "cdna_start": 3514,
          "cdna_end": null,
          "cdna_length": 9779,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3176A>G",
          "hgvs_p": "p.Lys1059Arg",
          "transcript": "XM_011510783.4",
          "protein_id": "XP_011509085.1",
          "transcript_support_level": null,
          "aa_start": 1059,
          "aa_end": null,
          "aa_length": 2054,
          "cds_start": 3176,
          "cds_end": null,
          "cds_length": 6165,
          "cdna_start": 3346,
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          "cdna_length": 9776,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "R",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3173A>G",
          "hgvs_p": "p.Lys1058Arg",
          "transcript": "XM_011510784.3",
          "protein_id": "XP_011509086.1",
          "transcript_support_level": null,
          "aa_start": 1058,
          "aa_end": null,
          "aa_length": 2053,
          "cds_start": 3173,
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          "cds_length": 6162,
          "cdna_start": 3343,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 20,
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          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3158A>G",
          "hgvs_p": "p.Lys1053Arg",
          "transcript": "XM_011510785.4",
          "protein_id": "XP_011509087.1",
          "transcript_support_level": null,
          "aa_start": 1053,
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          "aa_length": 2048,
          "cds_start": 3158,
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          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "K",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3308A>G",
          "hgvs_p": "p.Lys1103Arg",
          "transcript": "XM_047443670.1",
          "protein_id": "XP_047299626.1",
          "transcript_support_level": null,
          "aa_start": 1103,
          "aa_end": null,
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          "cds_start": 3308,
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          "cdna_start": 3478,
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        },
        {
          "aa_ref": "K",
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          "intron_rank": null,
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          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3140A>G",
          "hgvs_p": "p.Lys1047Arg",
          "transcript": "XM_047443671.1",
          "protein_id": "XP_047299627.1",
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3140A>G",
          "hgvs_p": "p.Lys1047Arg",
          "transcript": "XM_047443672.1",
          "protein_id": "XP_047299628.1",
          "transcript_support_level": null,
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          "cdna_start": 3367,
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          "mane_select": null,
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        {
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          "strand": true,
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          ],
          "exon_rank": 20,
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          "exon_count": 41,
          "intron_rank": null,
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          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3290A>G",
          "hgvs_p": "p.Lys1097Arg",
          "transcript": "XM_047443673.1",
          "protein_id": "XP_047299629.1",
          "transcript_support_level": null,
          "aa_start": 1097,
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        {
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          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3122A>G",
          "hgvs_p": "p.Lys1041Arg",
          "transcript": "XM_017003569.2",
          "protein_id": "XP_016859058.1",
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        },
        {
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          "strand": true,
          "consequences": [
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          ],
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          "intron_rank": null,
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          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3053A>G",
          "hgvs_p": "p.Lys1018Arg",
          "transcript": "XM_011510786.4",
          "protein_id": "XP_011509088.1",
          "transcript_support_level": null,
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          "aa_length": 2013,
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        },
        {
          "aa_ref": "K",
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PIKFYVE",
          "gene_hgnc_id": 23785,
          "hgvs_c": "c.3050A>G",
          "hgvs_p": "p.Lys1017Arg",
          "transcript": "XM_011510787.2",
          "protein_id": "XP_011509089.1",
          "transcript_support_level": null,
          "aa_start": 1017,
          "aa_end": null,
          "aa_length": 2012,
          "cds_start": 3050,
          "cds_end": null,
          "cds_length": 6039,
          "cdna_start": 3220,
          "cdna_end": null,
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          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "K",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "missense_variant"
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          "transcript": "ENST00000443896.5",
          "protein_id": "ENSP00000407692.1",
          "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": 3282,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "PIKFYVE",
      "gene_hgnc_id": 23785,
      "dbsnp": "rs121918336",
      "frequency_reference_population": 0.000001858667,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 3,
      "gnomad_exomes_af": 0.00000136811,
      "gnomad_genomes_af": 0.00000657082,
      "gnomad_exomes_ac": 2,
      "gnomad_genomes_ac": 1,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.8079017996788025,
      "computational_prediction_selected": "Pathogenic",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.28,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.1195,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.13,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 9.204,
      "phylop100way_prediction": "Pathogenic",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": 4,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2,PP3,PP5",
      "acmg_by_gene": [
        {
          "score": 4,
          "benign_score": 0,
          "pathogenic_score": 4,
          "criteria": [
            "PM2",
            "PP3",
            "PP5"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "ENST00000264380.9",
          "gene_symbol": "PIKFYVE",
          "hgnc_id": 23785,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.3308A>G",
          "hgvs_p": "p.Lys1103Arg"
        }
      ],
      "clinvar_disease": "Fleck corneal dystrophy",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "no assertion criteria provided",
      "clinvar_submissions_summary": "null",
      "phenotype_combined": "Fleck corneal dystrophy",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}