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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: 5-60918364-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=60918364&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "5",
      "pos": 60918364,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "ENST00000676185.1",
      "consequences": [
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "c.300C>T",
          "hgvs_p": "p.Tyr100Tyr",
          "transcript": "NM_000082.4",
          "protein_id": "NP_000073.1",
          "transcript_support_level": null,
          "aa_start": 100,
          "aa_end": null,
          "aa_length": 396,
          "cds_start": 300,
          "cds_end": null,
          "cds_length": 1191,
          "cdna_start": 362,
          "cdna_end": null,
          "cdna_length": 9414,
          "mane_select": "ENST00000676185.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "c.300C>T",
          "hgvs_p": "p.Tyr100Tyr",
          "transcript": "ENST00000676185.1",
          "protein_id": "ENSP00000501614.1",
          "transcript_support_level": null,
          "aa_start": 100,
          "aa_end": null,
          "aa_length": 396,
          "cds_start": 300,
          "cds_end": null,
          "cds_length": 1191,
          "cdna_start": 362,
          "cdna_end": null,
          "cdna_length": 9414,
          "mane_select": "NM_000082.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "c.300C>T",
          "hgvs_p": "p.Tyr100Tyr",
          "transcript": "ENST00000265038.10",
          "protein_id": "ENSP00000265038.6",
          "transcript_support_level": 1,
          "aa_start": 100,
          "aa_end": null,
          "aa_length": 415,
          "cds_start": 300,
          "cds_end": null,
          "cds_length": 1248,
          "cdna_start": 356,
          "cdna_end": null,
          "cdna_length": 2034,
          "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": 5,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "n.*98C>T",
          "hgvs_p": null,
          "transcript": "ENST00000497892.6",
          "protein_id": "ENSP00000501805.1",
          "transcript_support_level": 1,
          "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": 969,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "n.*98C>T",
          "hgvs_p": null,
          "transcript": "ENST00000497892.6",
          "protein_id": "ENSP00000501805.1",
          "transcript_support_level": 1,
          "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": 969,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "c.126C>T",
          "hgvs_p": "p.Tyr42Tyr",
          "transcript": "NM_001007233.3",
          "protein_id": "NP_001007234.1",
          "transcript_support_level": null,
          "aa_start": 42,
          "aa_end": null,
          "aa_length": 338,
          "cds_start": 126,
          "cds_end": null,
          "cds_length": 1017,
          "cdna_start": 580,
          "cdna_end": null,
          "cdna_length": 9632,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 5,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "c.126C>T",
          "hgvs_p": "p.Tyr42Tyr",
          "transcript": "ENST00000675042.2",
          "protein_id": "ENSP00000502082.2",
          "transcript_support_level": null,
          "aa_start": 42,
          "aa_end": null,
          "aa_length": 338,
          "cds_start": 126,
          "cds_end": null,
          "cds_length": 1017,
          "cdna_start": 407,
          "cdna_end": null,
          "cdna_length": 2091,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "c.300C>T",
          "hgvs_p": "p.Tyr100Tyr",
          "transcript": "ENST00000682217.1",
          "protein_id": "ENSP00000507570.1",
          "transcript_support_level": null,
          "aa_start": 100,
          "aa_end": null,
          "aa_length": 330,
          "cds_start": 300,
          "cds_end": null,
          "cds_length": 993,
          "cdna_start": 362,
          "cdna_end": null,
          "cdna_length": 3672,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "c.102C>T",
          "hgvs_p": "p.Tyr34Tyr",
          "transcript": "ENST00000683052.1",
          "protein_id": "ENSP00000507072.1",
          "transcript_support_level": null,
          "aa_start": 34,
          "aa_end": null,
          "aa_length": 330,
          "cds_start": 102,
          "cds_end": null,
          "cds_length": 993,
          "cdna_start": 102,
          "cdna_end": null,
          "cdna_length": 1738,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "c.300C>T",
          "hgvs_p": "p.Tyr100Tyr",
          "transcript": "ENST00000439176.6",
          "protein_id": "ENSP00000408344.2",
          "transcript_support_level": 5,
          "aa_start": 100,
          "aa_end": null,
          "aa_length": 307,
          "cds_start": 300,
          "cds_end": null,
          "cds_length": 924,
          "cdna_start": 362,
          "cdna_end": null,
          "cdna_length": 1741,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "c.300C>T",
          "hgvs_p": "p.Tyr100Tyr",
          "transcript": "NM_001007234.3",
          "protein_id": "NP_001007235.1",
          "transcript_support_level": null,
          "aa_start": 100,
          "aa_end": null,
          "aa_length": 205,
          "cds_start": 300,
          "cds_end": null,
          "cds_length": 618,
          "cdna_start": 362,
          "cdna_end": null,
          "cdna_length": 900,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Y",
          "aa_alt": "Y",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "c.300C>T",
          "hgvs_p": "p.Tyr100Tyr",
          "transcript": "ENST00000675229.1",
          "protein_id": "ENSP00000502154.1",
          "transcript_support_level": null,
          "aa_start": 100,
          "aa_end": null,
          "aa_length": 205,
          "cds_start": 300,
          "cds_end": null,
          "cds_length": 618,
          "cdna_start": 343,
          "cdna_end": null,
          "cdna_length": 881,
          "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": 5,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "n.*344C>T",
          "hgvs_p": null,
          "transcript": "ENST00000381118.7",
          "protein_id": "ENSP00000370510.3",
          "transcript_support_level": 2,
          "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": 2236,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8-AS1",
          "gene_hgnc_id": 40220,
          "hgvs_c": "n.214G>A",
          "hgvs_p": null,
          "transcript": "ENST00000457499.2",
          "protein_id": null,
          "transcript_support_level": 3,
          "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": 474,
          "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": 4,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "n.351C>T",
          "hgvs_p": null,
          "transcript": "ENST00000477893.1",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
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          "cdna_length": 752,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "n.127C>T",
          "hgvs_p": null,
          "transcript": "ENST00000484330.5",
          "protein_id": null,
          "transcript_support_level": 3,
          "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": 471,
          "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": 2,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "n.73C>T",
          "hgvs_p": null,
          "transcript": "ENST00000495985.5",
          "protein_id": null,
          "transcript_support_level": 5,
          "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": 582,
          "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": 5,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "n.*192C>T",
          "hgvs_p": null,
          "transcript": "ENST00000643034.1",
          "protein_id": "ENSP00000496080.1",
          "transcript_support_level": null,
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          "cdna_length": 2095,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "n.300C>T",
          "hgvs_p": null,
          "transcript": "ENST00000643708.1",
          "protein_id": "ENSP00000494199.1",
          "transcript_support_level": null,
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          "cdna_length": 2280,
          "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": 4,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "n.300C>T",
          "hgvs_p": null,
          "transcript": "ENST00000647431.2",
          "protein_id": "ENSP00000494726.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2072,
          "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": 4,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ERCC8",
          "gene_hgnc_id": 3439,
          "hgvs_c": "n.300C>T",
          "hgvs_p": null,
          "transcript": "ENST00000647486.2",
          "protein_id": "ENSP00000494466.2",
          "transcript_support_level": null,
          "aa_start": null,
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          "hgnc_id": 40220,
          "effects": [
            "non_coding_transcript_exon_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.214G>A",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "not provided",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}