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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: 15-74788737-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=74788737&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "15",
      "pos": 74788737,
      "ref": "G",
      "alt": "A",
      "effect": "intron_variant",
      "transcript": "NM_004383.3",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-66+6017G>A",
          "hgvs_p": null,
          "transcript": "NM_004383.3",
          "protein_id": "NP_004374.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 450,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1353,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000220003.14",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_004383.3"
        },
        {
          "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": 13,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-66+6017G>A",
          "hgvs_p": null,
          "transcript": "ENST00000220003.14",
          "protein_id": "ENSP00000220003.9",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 450,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1353,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_004383.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000220003.14"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "n.217+6017G>A",
          "hgvs_p": null,
          "transcript": "ENST00000563894.1",
          "protein_id": null,
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "retained_intron",
          "feature": "ENST00000563894.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-66+6017G>A",
          "hgvs_p": null,
          "transcript": "NM_001127190.2",
          "protein_id": "NP_001120662.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 450,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1353,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001127190.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-399+160G>A",
          "hgvs_p": null,
          "transcript": "NM_001354988.2",
          "protein_id": "NP_001341917.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 450,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1353,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001354988.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-87+6017G>A",
          "hgvs_p": null,
          "transcript": "NM_001387089.1",
          "protein_id": "NP_001374018.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 450,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1353,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001387089.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-66+4214G>A",
          "hgvs_p": null,
          "transcript": "NM_001387090.1",
          "protein_id": "NP_001374019.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 450,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1353,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001387090.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-195-2080G>A",
          "hgvs_p": null,
          "transcript": "NM_001387091.1",
          "protein_id": "NP_001374020.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 450,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1353,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001387091.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-87+6017G>A",
          "hgvs_p": null,
          "transcript": "NM_001387092.1",
          "protein_id": "NP_001374021.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 450,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1353,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001387092.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-66+4214G>A",
          "hgvs_p": null,
          "transcript": "NM_001387093.1",
          "protein_id": "NP_001374022.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 450,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1353,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001387093.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-66+6017G>A",
          "hgvs_p": null,
          "transcript": "ENST00000439220.6",
          "protein_id": "ENSP00000414764.2",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 450,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1353,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000439220.6"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-399+160G>A",
          "hgvs_p": null,
          "transcript": "ENST00000567571.5",
          "protein_id": "ENSP00000454906.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 450,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1353,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000567571.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-66+4214G>A",
          "hgvs_p": null,
          "transcript": "ENST00000858351.1",
          "protein_id": "ENSP00000528410.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 450,
          "cds_start": null,
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          "cds_length": 1353,
          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000858351.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-245-1021G>A",
          "hgvs_p": null,
          "transcript": "ENST00000858352.1",
          "protein_id": "ENSP00000528411.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 450,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1353,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000858352.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "intron_rank": 1,
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          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-66+6589G>A",
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          "transcript": "ENST00000858354.1",
          "protein_id": "ENSP00000528413.1",
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          "cds_start": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000858354.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 14,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-66+4214G>A",
          "hgvs_p": null,
          "transcript": "ENST00000858355.1",
          "protein_id": "ENSP00000528414.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 450,
          "cds_start": null,
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          "cds_length": 1353,
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          "biotype": "protein_coding",
          "feature": "ENST00000858355.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 14,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-195-2080G>A",
          "hgvs_p": null,
          "transcript": "ENST00000858356.1",
          "protein_id": "ENSP00000528415.1",
          "transcript_support_level": null,
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          "aa_length": 450,
          "cds_start": null,
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          "cdna_start": null,
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          "cdna_length": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": null,
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          ],
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          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-66+4214G>A",
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          "transcript": "ENST00000858357.1",
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          "biotype": "protein_coding",
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        },
        {
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          "canonical": false,
          "protein_coding": true,
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          ],
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          "exon_count": 14,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-66+716G>A",
          "hgvs_p": null,
          "transcript": "ENST00000931146.1",
          "protein_id": "ENSP00000601205.1",
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          "cds_start": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000931146.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 13,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "CSK",
          "gene_hgnc_id": 2444,
          "hgvs_c": "c.-66+6017G>A",
          "hgvs_p": null,
          "transcript": "NM_001387094.1",
          "protein_id": "NP_001374023.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 449,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1350,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001387094.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": 1,
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      "splice_source_selected": "max_spliceai",
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      "bayesdelnoaf_score": -0.85,
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      "spliceai_max_score": 0,
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      "acmg_score": -12,
      "acmg_classification": "Benign",
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      "acmg_by_gene": [
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          "verdict": "Benign",
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        {
          "score": -12,
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          "verdict": "Benign",
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          "gene_symbol": "MIR4513",
          "hgnc_id": 41855,
          "effects": [
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          "inheritance_mode": "",
          "hgvs_c": "n.21C>T",
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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
}