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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: 6-138908685-T-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=138908685&ref=T&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "6",
      "pos": 138908685,
      "ref": "T",
      "alt": "G",
      "effect": "synonymous_variant",
      "transcript": "NM_001286611.2",
      "consequences": [
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.2199A>C",
          "hgvs_p": "p.Ser733Ser",
          "transcript": "NM_001286611.2",
          "protein_id": "NP_001273540.1",
          "transcript_support_level": null,
          "aa_start": 733,
          "aa_end": null,
          "aa_length": 796,
          "cds_start": 2199,
          "cds_end": null,
          "cds_length": 2391,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000450536.7",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001286611.2"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.2199A>C",
          "hgvs_p": "p.Ser733Ser",
          "transcript": "ENST00000450536.7",
          "protein_id": "ENSP00000392065.2",
          "transcript_support_level": 1,
          "aa_start": 733,
          "aa_end": null,
          "aa_length": 796,
          "cds_start": 2199,
          "cds_end": null,
          "cds_length": 2391,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001286611.2",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000450536.7"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.2196A>C",
          "hgvs_p": "p.Ser732Ser",
          "transcript": "ENST00000258062.9",
          "protein_id": "ENSP00000258062.5",
          "transcript_support_level": 1,
          "aa_start": 732,
          "aa_end": null,
          "aa_length": 795,
          "cds_start": 2196,
          "cds_end": null,
          "cds_length": 2388,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000258062.9"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.1926A>C",
          "hgvs_p": "p.Ser642Ser",
          "transcript": "ENST00000409812.6",
          "protein_id": "ENSP00000386699.2",
          "transcript_support_level": 1,
          "aa_start": 642,
          "aa_end": null,
          "aa_length": 705,
          "cds_start": 1926,
          "cds_end": null,
          "cds_length": 2118,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000409812.6"
        },
        {
          "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": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "n.926A>C",
          "hgvs_p": null,
          "transcript": "ENST00000484164.6",
          "protein_id": null,
          "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": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "retained_intron",
          "feature": "ENST00000484164.6"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.2223A>C",
          "hgvs_p": "p.Ser741Ser",
          "transcript": "ENST00000913792.1",
          "protein_id": "ENSP00000583851.1",
          "transcript_support_level": null,
          "aa_start": 741,
          "aa_end": null,
          "aa_length": 804,
          "cds_start": 2223,
          "cds_end": null,
          "cds_length": 2415,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000913792.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.2214A>C",
          "hgvs_p": "p.Ser738Ser",
          "transcript": "ENST00000913794.1",
          "protein_id": "ENSP00000583853.1",
          "transcript_support_level": null,
          "aa_start": 738,
          "aa_end": null,
          "aa_length": 801,
          "cds_start": 2214,
          "cds_end": null,
          "cds_length": 2406,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000913794.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.2196A>C",
          "hgvs_p": "p.Ser732Ser",
          "transcript": "NM_031922.5",
          "protein_id": "NP_114128.3",
          "transcript_support_level": null,
          "aa_start": 732,
          "aa_end": null,
          "aa_length": 795,
          "cds_start": 2196,
          "cds_end": null,
          "cds_length": 2388,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_031922.5"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.2196A>C",
          "hgvs_p": "p.Ser732Ser",
          "transcript": "ENST00000886446.1",
          "protein_id": "ENSP00000556505.1",
          "transcript_support_level": null,
          "aa_start": 732,
          "aa_end": null,
          "aa_length": 795,
          "cds_start": 2196,
          "cds_end": null,
          "cds_length": 2388,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000886446.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.2193A>C",
          "hgvs_p": "p.Ser731Ser",
          "transcript": "ENST00000886454.1",
          "protein_id": "ENSP00000556513.1",
          "transcript_support_level": null,
          "aa_start": 731,
          "aa_end": null,
          "aa_length": 794,
          "cds_start": 2193,
          "cds_end": null,
          "cds_length": 2385,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000886454.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.2193A>C",
          "hgvs_p": "p.Ser731Ser",
          "transcript": "ENST00000913795.1",
          "protein_id": "ENSP00000583854.1",
          "transcript_support_level": null,
          "aa_start": 731,
          "aa_end": null,
          "aa_length": 794,
          "cds_start": 2193,
          "cds_end": null,
          "cds_length": 2385,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000913795.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.2157A>C",
          "hgvs_p": "p.Ser719Ser",
          "transcript": "ENST00000886449.1",
          "protein_id": "ENSP00000556508.1",
          "transcript_support_level": null,
          "aa_start": 719,
          "aa_end": null,
          "aa_length": 782,
          "cds_start": 2157,
          "cds_end": null,
          "cds_length": 2349,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000886449.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.2139A>C",
          "hgvs_p": "p.Ser713Ser",
          "transcript": "ENST00000968036.1",
          "protein_id": "ENSP00000638095.1",
          "transcript_support_level": null,
          "aa_start": 713,
          "aa_end": null,
          "aa_length": 776,
          "cds_start": 2139,
          "cds_end": null,
          "cds_length": 2331,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000968036.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.2136A>C",
          "hgvs_p": "p.Ser712Ser",
          "transcript": "ENST00000886450.1",
          "protein_id": "ENSP00000556510.1",
          "transcript_support_level": null,
          "aa_start": 712,
          "aa_end": null,
          "aa_length": 775,
          "cds_start": 2136,
          "cds_end": null,
          "cds_length": 2328,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000886450.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.2136A>C",
          "hgvs_p": "p.Ser712Ser",
          "transcript": "ENST00000968037.1",
          "protein_id": "ENSP00000638096.1",
          "transcript_support_level": null,
          "aa_start": 712,
          "aa_end": null,
          "aa_length": 775,
          "cds_start": 2136,
          "cds_end": null,
          "cds_length": 2328,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000968037.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.2133A>C",
          "hgvs_p": "p.Ser711Ser",
          "transcript": "ENST00000886452.1",
          "protein_id": "ENSP00000556511.1",
          "transcript_support_level": null,
          "aa_start": 711,
          "aa_end": null,
          "aa_length": 774,
          "cds_start": 2133,
          "cds_end": null,
          "cds_length": 2325,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000886452.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.2133A>C",
          "hgvs_p": "p.Ser711Ser",
          "transcript": "ENST00000886458.1",
          "protein_id": "ENSP00000556517.1",
          "transcript_support_level": null,
          "aa_start": 711,
          "aa_end": null,
          "aa_length": 774,
          "cds_start": 2133,
          "cds_end": null,
          "cds_length": 2325,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000886458.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.2130A>C",
          "hgvs_p": "p.Ser710Ser",
          "transcript": "ENST00000968035.1",
          "protein_id": "ENSP00000638094.1",
          "transcript_support_level": null,
          "aa_start": 710,
          "aa_end": null,
          "aa_length": 773,
          "cds_start": 2130,
          "cds_end": null,
          "cds_length": 2322,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000968035.1"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.2118A>C",
          "hgvs_p": "p.Ser706Ser",
          "transcript": "NM_001128617.3",
          "protein_id": "NP_001122089.1",
          "transcript_support_level": null,
          "aa_start": 706,
          "aa_end": null,
          "aa_length": 769,
          "cds_start": 2118,
          "cds_end": null,
          "cds_length": 2310,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001128617.3"
        },
        {
          "aa_ref": "S",
          "aa_alt": "S",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "REPS1",
          "gene_hgnc_id": 15578,
          "hgvs_c": "c.2118A>C",
          "hgvs_p": "p.Ser706Ser",
          "transcript": "ENST00000367663.8",
          "protein_id": "ENSP00000356635.4",
          "transcript_support_level": 5,
          "aa_start": 706,
          "aa_end": null,
          "aa_length": 769,
          "cds_start": 2118,
          "cds_end": null,
          "cds_length": 2310,
          "cdna_start": null,
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          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate",
            "BP6_Moderate",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_001286611.2",
          "gene_symbol": "REPS1",
          "hgnc_id": 15578,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "Unknown",
          "hgvs_c": "c.2199A>C",
          "hgvs_p": "p.Ser733Ser"
        }
      ],
      "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
}