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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: 9-112409029-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=112409029&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "9",
      "pos": 112409029,
      "ref": "T",
      "alt": "C",
      "effect": "splice_region_variant,intron_variant",
      "transcript": "NM_032303.5",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.395+8T>C",
          "hgvs_p": null,
          "transcript": "NM_032303.5",
          "protein_id": "NP_115679.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000398805.8",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_032303.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.395+8T>C",
          "hgvs_p": null,
          "transcript": "ENST00000398805.8",
          "protein_id": "ENSP00000381785.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 418,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1257,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_032303.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000398805.8"
        },
        {
          "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": 3,
          "intron_rank_end": null,
          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.280+3307T>C",
          "hgvs_p": null,
          "transcript": "ENST00000398803.1",
          "protein_id": "ENSP00000381783.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 345,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1038,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000398803.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.389+8T>C",
          "hgvs_p": null,
          "transcript": "ENST00000942135.1",
          "protein_id": "ENSP00000612194.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 416,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1251,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000942135.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.395+8T>C",
          "hgvs_p": null,
          "transcript": "ENST00000942137.1",
          "protein_id": "ENSP00000612196.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 416,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1251,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000942137.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.386+8T>C",
          "hgvs_p": null,
          "transcript": "ENST00000860570.1",
          "protein_id": "ENSP00000530629.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 415,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1248,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000860570.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.395+8T>C",
          "hgvs_p": null,
          "transcript": "ENST00000860574.1",
          "protein_id": "ENSP00000530633.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 392,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1179,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000860574.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.296+8T>C",
          "hgvs_p": null,
          "transcript": "ENST00000860569.1",
          "protein_id": "ENSP00000530628.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 385,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1158,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000860569.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.395+8T>C",
          "hgvs_p": null,
          "transcript": "ENST00000860575.1",
          "protein_id": "ENSP00000530634.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 385,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1158,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000860575.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.395+8T>C",
          "hgvs_p": null,
          "transcript": "ENST00000942139.1",
          "protein_id": "ENSP00000612198.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 375,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1128,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
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        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.395+8T>C",
          "hgvs_p": null,
          "transcript": "ENST00000860572.1",
          "protein_id": "ENSP00000530631.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 368,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1107,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000860572.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 10,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.395+8T>C",
          "hgvs_p": null,
          "transcript": "ENST00000860566.1",
          "protein_id": "ENSP00000530625.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 353,
          "cds_start": null,
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          "cds_length": 1062,
          "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": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 9,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.280+3307T>C",
          "hgvs_p": null,
          "transcript": "NM_001195822.2",
          "protein_id": "NP_001182751.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 345,
          "cds_start": null,
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          "cds_length": 1038,
          "cdna_start": null,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001195822.2"
        },
        {
          "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": 9,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.274+3307T>C",
          "hgvs_p": null,
          "transcript": "ENST00000942134.1",
          "protein_id": "ENSP00000612193.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 343,
          "cds_start": null,
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        },
        {
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            "intron_variant"
          ],
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          "intron_rank": 4,
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          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.395+8T>C",
          "hgvs_p": null,
          "transcript": "ENST00000860568.1",
          "protein_id": "ENSP00000530627.1",
          "transcript_support_level": null,
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          "cds_start": null,
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          "cds_length": 990,
          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000860568.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.280+3307T>C",
          "hgvs_p": null,
          "transcript": "ENST00000860567.1",
          "protein_id": "ENSP00000530626.1",
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          "aa_start": null,
          "aa_end": null,
          "aa_length": 312,
          "cds_start": null,
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          "cdna_start": null,
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          "cdna_length": null,
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        },
        {
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          "canonical": false,
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          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 8,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.181+4871T>C",
          "hgvs_p": null,
          "transcript": "ENST00000942136.1",
          "protein_id": "ENSP00000612195.1",
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        },
        {
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          ],
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          "exon_count": 8,
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          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.277+3307T>C",
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          "transcript": "ENST00000942140.1",
          "protein_id": "ENSP00000612199.1",
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        {
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          ],
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          "exon_count": 8,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.18-7812T>C",
          "hgvs_p": null,
          "transcript": "ENST00000860565.1",
          "protein_id": "ENSP00000530624.1",
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          "cds_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000860565.1"
        },
        {
          "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": 8,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "HSDL2",
          "gene_hgnc_id": 18572,
          "hgvs_c": "c.280+3307T>C",
          "hgvs_p": null,
          "transcript": "ENST00000929491.1",
          "protein_id": "ENSP00000599550.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 280,
          "cds_start": null,
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          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "criteria": [
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            "BP6_Very_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000656504.2",
          "gene_symbol": "HSDL2-AS1",
          "hgnc_id": 31438,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.420+893A>G",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "B:2",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Benign",
      "custom_annotations": null
    }
  ],
  "message": null
}