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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: 8-85110101-CTTTTTT-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=85110101&ref=CTTTTTT&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "8",
      "pos": 85110101,
      "ref": "CTTTTTT",
      "alt": "C",
      "effect": "splice_region_variant,intron_variant",
      "transcript": "NM_033402.5",
      "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": 19,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "c.311-8_311-3delTTTTTT",
          "hgvs_p": null,
          "transcript": "NM_033402.5",
          "protein_id": "NP_208325.3",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1032,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3099,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3726,
          "mane_select": "ENST00000360375.8",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_033402.5"
        },
        {
          "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": 19,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "c.311-13_311-8delTTTTTT",
          "hgvs_p": null,
          "transcript": "ENST00000360375.8",
          "protein_id": "ENSP00000353538.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1032,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3099,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3726,
          "mane_select": "NM_033402.5",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000360375.8"
        },
        {
          "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": 18,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "c.251-13_251-8delTTTTTT",
          "hgvs_p": null,
          "transcript": "ENST00000414626.2",
          "protein_id": "ENSP00000394695.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1012,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3039,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4493,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000414626.2"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "n.105-13_105-8delTTTTTT",
          "hgvs_p": null,
          "transcript": "ENST00000517875.5",
          "protein_id": "ENSP00000430960.1",
          "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": 2385,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000517875.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "n.105-13_105-8delTTTTTT",
          "hgvs_p": null,
          "transcript": "ENST00000522567.5",
          "protein_id": "ENSP00000428794.1",
          "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": 2122,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000522567.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "n.105-13_105-8delTTTTTT",
          "hgvs_p": null,
          "transcript": "ENST00000523669.5",
          "protein_id": "ENSP00000430878.1",
          "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": 1004,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000523669.5"
        },
        {
          "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": 20,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "c.311-13_311-8delTTTTTT",
          "hgvs_p": null,
          "transcript": "ENST00000926004.1",
          "protein_id": "ENSP00000596063.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1046,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 3141,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3619,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000926004.1"
        },
        {
          "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": 18,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "c.311-13_311-8delTTTTTT",
          "hgvs_p": null,
          "transcript": "ENST00000962243.1",
          "protein_id": "ENSP00000632302.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 970,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2913,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3297,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000962243.1"
        },
        {
          "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": 18,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "c.311-13_311-8delTTTTTT",
          "hgvs_p": null,
          "transcript": "ENST00000926003.1",
          "protein_id": "ENSP00000596062.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 962,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2889,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3458,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000926003.1"
        },
        {
          "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": 18,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "c.32-8_32-3delTTTTTT",
          "hgvs_p": null,
          "transcript": "NM_001349636.2",
          "protein_id": "NP_001336565.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 939,
          "cds_start": null,
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          "cds_length": 2820,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3520,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001349636.2"
        },
        {
          "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": 19,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "c.-158-8_-158-3delTTTTTT",
          "hgvs_p": null,
          "transcript": "NM_001349637.2",
          "protein_id": "NP_001336566.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 890,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2673,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3881,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001349637.2"
        },
        {
          "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": 17,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "c.-201-8_-201-3delTTTTTT",
          "hgvs_p": null,
          "transcript": "NM_001349638.2",
          "protein_id": "NP_001336567.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 733,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2202,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3340,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001349638.2"
        },
        {
          "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": 15,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "c.-247-8_-247-3delTTTTTT",
          "hgvs_p": null,
          "transcript": "NM_001349639.2",
          "protein_id": "NP_001336568.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 653,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1962,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2940,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001349639.2"
        },
        {
          "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": 20,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "c.311-8_311-3delTTTTTT",
          "hgvs_p": null,
          "transcript": "XM_017013920.2",
          "protein_id": "XP_016869409.1",
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          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
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          "canonical": false,
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          "strand": true,
          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 20,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "c.311-8_311-3delTTTTTT",
          "hgvs_p": null,
          "transcript": "XM_017013921.2",
          "protein_id": "XP_016869410.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1025,
          "cds_start": null,
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          "cds_length": 3078,
          "cdna_start": null,
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          "cdna_length": 3705,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "XM_017013921.2"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "c.311-8_311-3delTTTTTT",
          "hgvs_p": null,
          "transcript": "XM_047422364.1",
          "protein_id": "XP_047278320.1",
          "transcript_support_level": null,
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          "aa_length": 1011,
          "cds_start": null,
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          "cds_length": 3036,
          "cdna_start": null,
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          "cdna_length": 3663,
          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "XM_047422364.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 19,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "c.311-8_311-3delTTTTTT",
          "hgvs_p": null,
          "transcript": "XM_017013922.2",
          "protein_id": "XP_016869411.1",
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        },
        {
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          "canonical": false,
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          "strand": true,
          "consequences": [
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            "intron_variant"
          ],
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          "exon_count": 18,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "c.311-8_311-3delTTTTTT",
          "hgvs_p": null,
          "transcript": "XM_047422365.1",
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          "cds_start": null,
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          "cdna_start": null,
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          "biotype": "protein_coding",
          "feature": "XM_047422365.1"
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "LRRCC1",
          "gene_hgnc_id": 29373,
          "hgvs_c": "c.32-8_32-3delTTTTTT",
          "hgvs_p": null,
          "transcript": "XM_017013923.2",
          "protein_id": "XP_016869412.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 953,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2862,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3562,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_017013923.2"
        },
        {
          "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": 18,
          "intron_rank": 1,
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          "gene_symbol": "E2F5-DT",
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          "effects": [
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      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
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      "custom_annotations": null
    }
  ],
  "message": null
}
For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.