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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: 6-8419662-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=8419662&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "6",
      "pos": 8419662,
      "ref": "G",
      "alt": "A",
      "effect": "missense_variant",
      "transcript": "NM_001370476.2",
      "consequences": [
        {
          "aa_ref": "S",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC35B3",
          "gene_hgnc_id": 21601,
          "hgvs_c": "c.698C>T",
          "hgvs_p": "p.Ser233Phe",
          "transcript": "NM_001370476.2",
          "protein_id": "NP_001357405.1",
          "transcript_support_level": null,
          "aa_start": 233,
          "aa_end": null,
          "aa_length": 401,
          "cds_start": 698,
          "cds_end": null,
          "cds_length": 1206,
          "cdna_start": 944,
          "cdna_end": null,
          "cdna_length": 3566,
          "mane_select": "ENST00000644923.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC35B3",
          "gene_hgnc_id": 21601,
          "hgvs_c": "c.698C>T",
          "hgvs_p": "p.Ser233Phe",
          "transcript": "ENST00000644923.2",
          "protein_id": "ENSP00000496368.1",
          "transcript_support_level": null,
          "aa_start": 233,
          "aa_end": null,
          "aa_length": 401,
          "cds_start": 698,
          "cds_end": null,
          "cds_length": 1206,
          "cdna_start": 944,
          "cdna_end": null,
          "cdna_length": 3566,
          "mane_select": "NM_001370476.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC35B3",
          "gene_hgnc_id": 21601,
          "hgvs_c": "c.698C>T",
          "hgvs_p": "p.Ser233Phe",
          "transcript": "ENST00000379660.4",
          "protein_id": "ENSP00000368981.4",
          "transcript_support_level": 1,
          "aa_start": 233,
          "aa_end": null,
          "aa_length": 401,
          "cds_start": 698,
          "cds_end": null,
          "cds_length": 1206,
          "cdna_start": 1148,
          "cdna_end": null,
          "cdna_length": 2137,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "F",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC35B3",
          "gene_hgnc_id": 21601,
          "hgvs_c": "c.602C>T",
          "hgvs_p": "p.Ser201Phe",
          "transcript": "ENST00000710437.1",
          "protein_id": "ENSP00000518269.1",
          "transcript_support_level": null,
          "aa_start": 201,
          "aa_end": null,
          "aa_length": 369,
          "cds_start": 602,
          "cds_end": null,
          "cds_length": 1110,
          "cdna_start": 898,
          "cdna_end": null,
          "cdna_length": 3520,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC35B3",
          "gene_hgnc_id": 21601,
          "hgvs_c": "c.698C>T",
          "hgvs_p": "p.Ser233Phe",
          "transcript": "NM_001142540.2",
          "protein_id": "NP_001136012.1",
          "transcript_support_level": null,
          "aa_start": 233,
          "aa_end": null,
          "aa_length": 401,
          "cds_start": 698,
          "cds_end": null,
          "cds_length": 1206,
          "cdna_start": 1059,
          "cdna_end": null,
          "cdna_length": 3681,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC35B3",
          "gene_hgnc_id": 21601,
          "hgvs_c": "c.698C>T",
          "hgvs_p": "p.Ser233Phe",
          "transcript": "NM_001142541.3",
          "protein_id": "NP_001136013.1",
          "transcript_support_level": null,
          "aa_start": 233,
          "aa_end": null,
          "aa_length": 401,
          "cds_start": 698,
          "cds_end": null,
          "cds_length": 1206,
          "cdna_start": 848,
          "cdna_end": null,
          "cdna_length": 3470,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC35B3",
          "gene_hgnc_id": 21601,
          "hgvs_c": "c.698C>T",
          "hgvs_p": "p.Ser233Phe",
          "transcript": "NM_015948.5",
          "protein_id": "NP_057032.2",
          "transcript_support_level": null,
          "aa_start": 233,
          "aa_end": null,
          "aa_length": 401,
          "cds_start": 698,
          "cds_end": null,
          "cds_length": 1206,
          "cdna_start": 1210,
          "cdna_end": null,
          "cdna_length": 3832,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC35B3",
          "gene_hgnc_id": 21601,
          "hgvs_c": "c.602C>T",
          "hgvs_p": "p.Ser201Phe",
          "transcript": "NM_001370478.2",
          "protein_id": "NP_001357407.2",
          "transcript_support_level": null,
          "aa_start": 201,
          "aa_end": null,
          "aa_length": 369,
          "cds_start": 602,
          "cds_end": null,
          "cds_length": 1110,
          "cdna_start": 1013,
          "cdna_end": null,
          "cdna_length": 2002,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC35B3",
          "gene_hgnc_id": 21601,
          "hgvs_c": "c.602C>T",
          "hgvs_p": "p.Ser201Phe",
          "transcript": "NM_001370479.2",
          "protein_id": "NP_001357408.1",
          "transcript_support_level": null,
          "aa_start": 201,
          "aa_end": null,
          "aa_length": 369,
          "cds_start": 602,
          "cds_end": null,
          "cds_length": 1110,
          "cdna_start": 898,
          "cdna_end": null,
          "cdna_length": 3520,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC35B3",
          "gene_hgnc_id": 21601,
          "hgvs_c": "c.602C>T",
          "hgvs_p": "p.Ser201Phe",
          "transcript": "ENST00000648987.1",
          "protein_id": "ENSP00000498054.1",
          "transcript_support_level": null,
          "aa_start": 201,
          "aa_end": null,
          "aa_length": 369,
          "cds_start": 602,
          "cds_end": null,
          "cds_length": 1110,
          "cdna_start": 739,
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          "cdna_length": 1911,
          "mane_select": null,
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        },
        {
          "aa_ref": "S",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 6,
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          "exon_count": 9,
          "intron_rank": null,
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          "gene_symbol": "SLC35B3",
          "gene_hgnc_id": 21601,
          "hgvs_c": "c.602C>T",
          "hgvs_p": "p.Ser201Phe",
          "transcript": "NM_001370477.1",
          "protein_id": "NP_001357406.1",
          "transcript_support_level": null,
          "aa_start": 201,
          "aa_end": null,
          "aa_length": 338,
          "cds_start": 602,
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          "cds_length": 1017,
          "cdna_start": 920,
          "cdna_end": null,
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          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": "S",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 6,
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          "exon_count": 10,
          "intron_rank": null,
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          "gene_symbol": "SLC35B3",
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          "hgvs_c": "c.1028C>T",
          "hgvs_p": "p.Ser343Phe",
          "transcript": "XM_047418840.1",
          "protein_id": "XP_047274796.1",
          "transcript_support_level": null,
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          "cds_start": 1028,
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          "cdna_start": 1164,
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        {
          "aa_ref": "S",
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          "strand": false,
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          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
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          "gene_symbol": "SLC35B3",
          "gene_hgnc_id": 21601,
          "hgvs_c": "c.1028C>T",
          "hgvs_p": "p.Ser343Phe",
          "transcript": "XM_047418841.1",
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          "cds_start": 1028,
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        },
        {
          "aa_ref": "S",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
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          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC35B3",
          "gene_hgnc_id": 21601,
          "hgvs_c": "c.698C>T",
          "hgvs_p": "p.Ser233Phe",
          "transcript": "XM_017010910.2",
          "protein_id": "XP_016866399.1",
          "transcript_support_level": null,
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          "aa_length": 401,
          "cds_start": 698,
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          "mane_select": null,
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        },
        {
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          ],
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          "gene_symbol": "SLC35B3",
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          "hgvs_c": "c.698C>T",
          "hgvs_p": "p.Ser233Phe",
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          "feature": null
        },
        {
          "aa_ref": "S",
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 6,
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          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC35B3",
          "gene_hgnc_id": 21601,
          "hgvs_c": "c.704C>T",
          "hgvs_p": "p.Ser235Phe",
          "transcript": "XM_006715103.4",
          "protein_id": "XP_006715166.1",
          "transcript_support_level": null,
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          "cds_start": 704,
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        },
        {
          "aa_ref": "S",
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          "exon_rank": 7,
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          "exon_count": 10,
          "intron_rank": null,
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          "gene_symbol": "SLC35B3",
          "gene_hgnc_id": 21601,
          "hgvs_c": "c.698C>T",
          "hgvs_p": "p.Ser233Phe",
          "transcript": "XM_017010912.3",
          "protein_id": "XP_016866401.1",
          "transcript_support_level": null,
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          "aa_length": 370,
          "cds_start": 698,
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        },
        {
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          "intron_rank": null,
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          "gene_symbol": "SLC35B3",
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          "hgvs_c": "c.698C>T",
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        },
        {
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          "intron_rank": null,
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          "gene_symbol": "SLC35B3",
          "gene_hgnc_id": 21601,
          "hgvs_c": "c.602C>T",
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          "transcript": "XM_011514648.2",
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        },
        {
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          ],
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          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SLC35B3",
          "gene_hgnc_id": 21601,
          "hgvs_c": "c.602C>T",
          "hgvs_p": "p.Ser201Phe",
          "transcript": "XM_047418842.1",
          "protein_id": "XP_047274798.1",
          "transcript_support_level": null,
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          "cdna_start": 802,
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          "cdna_length": 3424,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
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          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
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      "clinvar_disease": "not specified",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "not specified",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}