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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: 1-114719746-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=114719746&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "1",
      "pos": 114719746,
      "ref": "A",
      "alt": "G",
      "effect": "splice_region_variant,intron_variant",
      "transcript": "NM_001242891.2",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": 17,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.2053-4T>C",
          "hgvs_p": null,
          "transcript": "NM_001007553.3",
          "protein_id": "NP_001007554.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 798,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2397,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000358528.9",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001007553.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": 17,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.2053-4T>C",
          "hgvs_p": null,
          "transcript": "ENST00000358528.9",
          "protein_id": "ENSP00000351329.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 798,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2397,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001007553.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000358528.9"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": 17,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.2098-4T>C",
          "hgvs_p": null,
          "transcript": "ENST00000369530.5",
          "protein_id": "ENSP00000358543.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 813,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2442,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000369530.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.2053-4T>C",
          "hgvs_p": null,
          "transcript": "ENST00000438362.7",
          "protein_id": "ENSP00000407724.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 798,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2397,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000438362.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 15,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.1960-4T>C",
          "hgvs_p": null,
          "transcript": "ENST00000261443.9",
          "protein_id": "ENSP00000261443.5",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 767,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2304,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000261443.9"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.1960-4T>C",
          "hgvs_p": null,
          "transcript": "ENST00000339438.10",
          "protein_id": "ENSP00000342408.6",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 767,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2304,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000339438.10"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.2191-4T>C",
          "hgvs_p": null,
          "transcript": "NM_001242891.2",
          "protein_id": "NP_001229820.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 844,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2535,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001242891.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.2191-4T>C",
          "hgvs_p": null,
          "transcript": "ENST00000610726.5",
          "protein_id": "ENSP00000481762.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 844,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2535,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000610726.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.2191-4T>C",
          "hgvs_p": null,
          "transcript": "ENST00000688211.1",
          "protein_id": "ENSP00000508995.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 844,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2535,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000688211.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.2101-4T>C",
          "hgvs_p": null,
          "transcript": "ENST00000967184.1",
          "protein_id": "ENSP00000637243.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 814,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2445,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000967184.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": 17,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.2098-4T>C",
          "hgvs_p": null,
          "transcript": "NM_001130523.3",
          "protein_id": "NP_001123995.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 813,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2442,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001130523.3"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.2053-4T>C",
          "hgvs_p": null,
          "transcript": "NM_001242892.2",
          "protein_id": "NP_001229821.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 798,
          "cds_start": null,
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          "cds_length": 2397,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001242892.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.2053-4T>C",
          "hgvs_p": null,
          "transcript": "ENST00000534699.5",
          "protein_id": "ENSP00000432958.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 798,
          "cds_start": null,
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          "cds_length": 2397,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000534699.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.2053-4T>C",
          "hgvs_p": null,
          "transcript": "ENST00000689217.1",
          "protein_id": "ENSP00000508874.1",
          "transcript_support_level": null,
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          "cds_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": 17,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.2053-4T>C",
          "hgvs_p": null,
          "transcript": "ENST00000689989.1",
          "protein_id": "ENSP00000509808.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 798,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2397,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000689989.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.2053-4T>C",
          "hgvs_p": null,
          "transcript": "ENST00000692719.1",
          "protein_id": "ENSP00000510208.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 798,
          "cds_start": null,
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          "cdna_start": null,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000692719.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.2053-4T>C",
          "hgvs_p": null,
          "transcript": "ENST00000901466.1",
          "protein_id": "ENSP00000571525.1",
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          "cds_start": null,
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          "cdna_start": null,
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        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.2053-4T>C",
          "hgvs_p": null,
          "transcript": "ENST00000901467.1",
          "protein_id": "ENSP00000571526.1",
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
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          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 18,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.2053-4T>C",
          "hgvs_p": null,
          "transcript": "ENST00000901476.1",
          "protein_id": "ENSP00000571535.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 798,
          "cds_start": null,
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          "cds_length": 2397,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000901476.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "CSDE1",
          "gene_hgnc_id": 29905,
          "hgvs_c": "c.2053-4T>C",
          "hgvs_p": null,
          "transcript": "ENST00000901484.1",
          "protein_id": "ENSP00000571543.1",
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          "transcript": "ENST00000693644.1",
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          "biotype": "retained_intron",
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      ],
      "gene_symbol": "CSDE1",
      "gene_hgnc_id": 29905,
      "dbsnp": "rs202150406",
      "frequency_reference_population": 0.0021795505,
      "hom_count_reference_population": 3,
      "allele_count_reference_population": 3219,
      "gnomad_exomes_af": 0.00227213,
      "gnomad_genomes_af": 0.00136036,
      "gnomad_exomes_ac": 3015,
      "gnomad_genomes_ac": 204,
      "gnomad_exomes_homalt": 3,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.8299999833106995,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.2639999985694885,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "dbscSNV1_RF",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.83,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.062,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": 0.000106019045223405,
      "dbscsnv_ada_prediction": "Benign",
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -14,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Moderate,BS1,BS2",
      "acmg_by_gene": [
        {
          "score": -14,
          "benign_score": 14,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Moderate",
            "BS1",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "NM_001242891.2",
          "gene_symbol": "CSDE1",
          "hgnc_id": 29905,
          "effects": [
            "splice_region_variant",
            "intron_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.2191-4T>C",
          "hgvs_p": null
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      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "B:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}