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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: 1-11786602-ATTTTT-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=11786602&ref=ATTTTT&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "1",
      "pos": 11786602,
      "ref": "ATTTTT",
      "alt": "A",
      "effect": "3_prime_UTR_variant",
      "transcript": "NM_001330358.2",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MTHFR",
          "gene_hgnc_id": 7436,
          "hgvs_c": "c.*4073_*4077delAAAAA",
          "hgvs_p": null,
          "transcript": "NM_005957.5",
          "protein_id": "NP_005948.3",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 656,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1971,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000376590.9",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_005957.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MTHFR",
          "gene_hgnc_id": 7436,
          "hgvs_c": "c.*4073_*4077delAAAAA",
          "hgvs_p": null,
          "transcript": "ENST00000376590.9",
          "protein_id": "ENSP00000365775.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 656,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1971,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_005957.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000376590.9"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MTHFR",
          "gene_hgnc_id": 7436,
          "hgvs_c": "c.*4073_*4077delAAAAA",
          "hgvs_p": null,
          "transcript": "ENST00000376592.6",
          "protein_id": "ENSP00000365777.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 656,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1971,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000376592.6"
        },
        {
          "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": 21,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "C1orf167",
          "gene_hgnc_id": 25262,
          "hgvs_c": "c.3568-771_3568-767delTTTTT",
          "hgvs_p": null,
          "transcript": "NM_001010881.2",
          "protein_id": "NP_001010881.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1449,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 4350,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000688073.1",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001010881.2"
        },
        {
          "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": 21,
          "intron_rank": 16,
          "intron_rank_end": null,
          "gene_symbol": "C1orf167",
          "gene_hgnc_id": 25262,
          "hgvs_c": "c.3568-771_3568-767delTTTTT",
          "hgvs_p": null,
          "transcript": "ENST00000688073.1",
          "protein_id": "ENSP00000510540.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1449,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 4350,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001010881.2",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000688073.1"
        },
        {
          "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": 10,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "C1orf167",
          "gene_hgnc_id": 25262,
          "hgvs_c": "c.1066-771_1066-767delTTTTT",
          "hgvs_p": null,
          "transcript": "ENST00000444493.5",
          "protein_id": "ENSP00000398213.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 615,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1848,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000444493.5"
        },
        {
          "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": 9,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "C1orf167",
          "gene_hgnc_id": 25262,
          "hgvs_c": "c.895-771_895-767delTTTTT",
          "hgvs_p": null,
          "transcript": "ENST00000449278.1",
          "protein_id": "ENSP00000399272.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 531,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1596,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000449278.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MTHFR",
          "gene_hgnc_id": 7436,
          "hgvs_c": "c.*4073_*4077delAAAAA",
          "hgvs_p": null,
          "transcript": "ENST00000911084.1",
          "protein_id": "ENSP00000581143.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 606,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1821,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000911084.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MTHFR",
          "gene_hgnc_id": 7436,
          "hgvs_c": "c.*4073_*4077delAAAAA",
          "hgvs_p": null,
          "transcript": "NM_001330358.2",
          "protein_id": "NP_001317287.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 697,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2094,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001330358.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MTHFR",
          "gene_hgnc_id": 7436,
          "hgvs_c": "c.*4073_*4077delAAAAA",
          "hgvs_p": null,
          "transcript": "ENST00000376583.7",
          "protein_id": "ENSP00000365767.3",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 697,
          "cds_start": null,
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          "cds_length": 2094,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MTHFR",
          "gene_hgnc_id": 7436,
          "hgvs_c": "c.*4073_*4077delAAAAA",
          "hgvs_p": null,
          "transcript": "ENST00000376585.6",
          "protein_id": "ENSP00000365770.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 697,
          "cds_start": null,
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          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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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": [
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          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
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          "gene_symbol": "MTHFR",
          "gene_hgnc_id": 7436,
          "hgvs_c": "c.*4073_*4077delAAAAA",
          "hgvs_p": null,
          "transcript": "NM_001410750.1",
          "protein_id": "NP_001397679.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": null,
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          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
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        {
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
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          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
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          "gene_symbol": "MTHFR",
          "gene_hgnc_id": 7436,
          "hgvs_c": "c.*4073_*4077delAAAAA",
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          "transcript": "ENST00000911084.1",
          "protein_id": "ENSP00000581143.1",
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          "cds_start": null,
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MTHFR",
          "gene_hgnc_id": 7436,
          "hgvs_c": "c.*3933_*3937delAAAAA",
          "hgvs_p": null,
          "transcript": "XM_011541496.4",
          "protein_id": "XP_011539798.1",
          "transcript_support_level": null,
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          "cds_start": null,
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        {
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          "gene_symbol": "MTHFR",
          "gene_hgnc_id": 7436,
          "hgvs_c": "c.*3933_*3937delAAAAA",
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          "transcript": "XM_047421174.1",
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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": 12,
          "intron_rank": null,
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          "gene_symbol": "MTHFR",
          "gene_hgnc_id": 7436,
          "hgvs_c": "c.*4073_*4077delAAAAA",
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          "transcript": "XM_005263462.5",
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        {
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          "canonical": false,
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          "consequences": [
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          ],
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          "exon_count": 12,
          "intron_rank": null,
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          "gene_symbol": "MTHFR",
          "gene_hgnc_id": 7436,
          "hgvs_c": "c.*4073_*4077delAAAAA",
          "hgvs_p": null,
          "transcript": "XM_047421178.1",
          "protein_id": "XP_047277134.1",
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        {
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          "intron_rank": null,
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          "transcript": "XM_017001328.3",
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        {
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          "gene_symbol": "MTHFR",
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MTHFR",
          "gene_hgnc_id": 7436,
          "hgvs_c": "c.*4073_*4077delAAAAA",
          "hgvs_p": null,
          "transcript": "XM_047421180.1",
          "protein_id": "XP_047277136.1",
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          "inheritance_mode": "AR",
          "hgvs_c": "c.*4073_*4077delAAAAA",
          "hgvs_p": null
        },
        {
          "score": 0,
          "benign_score": 0,
          "pathogenic_score": 0,
          "criteria": [],
          "verdict": "Uncertain_significance",
          "transcript": "NM_001010881.2",
          "gene_symbol": "C1orf167",
          "hgnc_id": 25262,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.3568-771_3568-767delTTTTT",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}