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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: 2-86254816-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=86254816&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 86254816,
      "ref": "T",
      "alt": "C",
      "effect": "splice_acceptor_variant,intron_variant",
      "transcript": "ENST00000538924.7",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "c.183-2A>G",
          "hgvs_p": null,
          "transcript": "NM_001371279.1",
          "protein_id": "NP_001358208.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 284,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 855,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4017,
          "mane_select": "ENST00000538924.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "c.183-2A>G",
          "hgvs_p": null,
          "transcript": "ENST00000538924.7",
          "protein_id": "ENSP00000438346.3",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 284,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 855,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4017,
          "mane_select": "NM_001371279.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "c.183-2A>G",
          "hgvs_p": null,
          "transcript": "ENST00000165698.9",
          "protein_id": "ENSP00000165698.5",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 201,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 606,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3857,
          "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": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "n.203A>G",
          "hgvs_p": null,
          "transcript": "ENST00000490915.5",
          "protein_id": null,
          "transcript_support_level": 4,
          "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": 566,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "c.141-2A>G",
          "hgvs_p": null,
          "transcript": "ENST00000642243.1",
          "protein_id": "ENSP00000494960.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 320,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 963,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1485,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "c.141-2A>G",
          "hgvs_p": null,
          "transcript": "ENST00000644644.1",
          "protein_id": "ENSP00000494305.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 287,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 864,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2584,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "c.183-2A>G",
          "hgvs_p": null,
          "transcript": "NM_001410855.1",
          "protein_id": "NP_001397784.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 272,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 819,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3981,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "c.183-2A>G",
          "hgvs_p": null,
          "transcript": "ENST00000643817.2",
          "protein_id": "ENSP00000495610.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 272,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 819,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2384,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "c.102-2A>G",
          "hgvs_p": null,
          "transcript": "ENST00000686220.1",
          "protein_id": "ENSP00000509904.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 223,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 672,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2882,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "c.183-2A>G",
          "hgvs_p": null,
          "transcript": "NM_001410856.1",
          "protein_id": "NP_001397785.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 213,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 642,
          "cdna_start": null,
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          "cdna_length": 3865,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "c.183-2A>G",
          "hgvs_p": null,
          "transcript": "ENST00000691703.1",
          "protein_id": "ENSP00000508496.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 213,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 642,
          "cdna_start": null,
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          "cdna_length": 1046,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "c.204-2A>G",
          "hgvs_p": null,
          "transcript": "NM_001164730.2",
          "protein_id": "NP_001158202.1",
          "transcript_support_level": null,
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          "aa_length": 208,
          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
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        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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          ],
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          "exon_count": 7,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "c.204-2A>G",
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          "transcript": "ENST00000453231.6",
          "protein_id": "ENSP00000392197.2",
          "transcript_support_level": 2,
          "aa_start": null,
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          "cds_start": -4,
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        },
        {
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          "canonical": false,
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          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 7,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "c.183-2A>G",
          "hgvs_p": null,
          "transcript": "NM_022912.3",
          "protein_id": "NP_075063.1",
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          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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          "biotype": null,
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        {
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          "intron_rank": 2,
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          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "c.102-2A>G",
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          "transcript": "NM_001164731.2",
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          "mane_select": null,
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          "biotype": null,
          "feature": null
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        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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            "intron_variant"
          ],
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          "exon_count": 6,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "c.102-2A>G",
          "hgvs_p": null,
          "transcript": "ENST00000535845.6",
          "protein_id": "ENSP00000437567.1",
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          "aa_start": null,
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          "aa_length": 174,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 1196,
          "mane_select": null,
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          "feature": null
        },
        {
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          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 6,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "c.183-2A>G",
          "hgvs_p": null,
          "transcript": "NM_001371280.1",
          "protein_id": "NP_001358209.1",
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          "cds_start": -4,
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          "cdna_start": null,
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        {
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          ],
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          "intron_rank": 3,
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          "gene_symbol": "REEP1",
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          "hgvs_c": "c.183-2A>G",
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          "transcript": "ENST00000689156.1",
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        },
        {
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          "strand": false,
          "consequences": [
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            "intron_variant"
          ],
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          "exon_count": 5,
          "intron_rank": 1,
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          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "c.33-2A>G",
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          "transcript": "ENST00000692664.1",
          "protein_id": "ENSP00000508656.1",
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          "mane_select": null,
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_acceptor_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 4,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "REEP1",
          "gene_hgnc_id": 25786,
          "hgvs_c": "c.117-2A>G",
          "hgvs_p": null,
          "transcript": "ENST00000489855.2",
          "protein_id": "ENSP00000475269.1",
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 146,
          "cds_start": -4,
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          "cds_length": 441,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 958,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
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      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "P:1",
      "phenotype_combined": "Hereditary spastic paraplegia 31",
      "pathogenicity_classification_combined": "Pathogenic",
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}