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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: 10-53857186-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=53857186&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "10",
      "pos": 53857186,
      "ref": "T",
      "alt": "C",
      "effect": "synonymous_variant",
      "transcript": "ENST00000644397.2",
      "consequences": [
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "c.3795A>G",
          "hgvs_p": "p.Glu1265Glu",
          "transcript": "NM_033056.4",
          "protein_id": "NP_149045.3",
          "transcript_support_level": null,
          "aa_start": 1265,
          "aa_end": null,
          "aa_length": 1955,
          "cds_start": 3795,
          "cds_end": null,
          "cds_length": 5868,
          "cdna_start": 4130,
          "cdna_end": null,
          "cdna_length": 6962,
          "mane_select": null,
          "mane_plus": "ENST00000320301.11",
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "c.3795A>G",
          "hgvs_p": "p.Glu1265Glu",
          "transcript": "ENST00000320301.11",
          "protein_id": "ENSP00000322604.6",
          "transcript_support_level": 1,
          "aa_start": 1265,
          "aa_end": null,
          "aa_length": 1955,
          "cds_start": 3795,
          "cds_end": null,
          "cds_length": 5868,
          "cdna_start": 4130,
          "cdna_end": null,
          "cdna_length": 6962,
          "mane_select": null,
          "mane_plus": "NM_033056.4",
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 38,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "c.3795A>G",
          "hgvs_p": "p.Glu1265Glu",
          "transcript": "NM_001384140.1",
          "protein_id": "NP_001371069.1",
          "transcript_support_level": null,
          "aa_start": 1265,
          "aa_end": null,
          "aa_length": 1740,
          "cds_start": 3795,
          "cds_end": null,
          "cds_length": 5223,
          "cdna_start": 4130,
          "cdna_end": null,
          "cdna_length": 9366,
          "mane_select": "ENST00000644397.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 38,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "c.3795A>G",
          "hgvs_p": "p.Glu1265Glu",
          "transcript": "ENST00000644397.2",
          "protein_id": "ENSP00000495195.1",
          "transcript_support_level": null,
          "aa_start": 1265,
          "aa_end": null,
          "aa_length": 1740,
          "cds_start": 3795,
          "cds_end": null,
          "cds_length": 5223,
          "cdna_start": 4130,
          "cdna_end": null,
          "cdna_length": 9366,
          "mane_select": "NM_001384140.1",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 35,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "c.3816A>G",
          "hgvs_p": "p.Glu1272Glu",
          "transcript": "ENST00000395445.6",
          "protein_id": "ENSP00000378832.2",
          "transcript_support_level": 1,
          "aa_start": 1272,
          "aa_end": null,
          "aa_length": 1783,
          "cds_start": 3816,
          "cds_end": null,
          "cds_length": 5352,
          "cdna_start": 4151,
          "cdna_end": null,
          "cdna_length": 6309,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 34,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "c.3795A>G",
          "hgvs_p": "p.Glu1265Glu",
          "transcript": "ENST00000616114.4",
          "protein_id": "ENSP00000483745.1",
          "transcript_support_level": 1,
          "aa_start": 1265,
          "aa_end": null,
          "aa_length": 1675,
          "cds_start": 3795,
          "cds_end": null,
          "cds_length": 5028,
          "cdna_start": 4190,
          "cdna_end": null,
          "cdna_length": 5846,
          "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": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "n.814A>G",
          "hgvs_p": null,
          "transcript": "ENST00000463095.2",
          "protein_id": null,
          "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": 3469,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 35,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "c.3810A>G",
          "hgvs_p": "p.Glu1270Glu",
          "transcript": "NM_001142763.2",
          "protein_id": "NP_001136235.1",
          "transcript_support_level": null,
          "aa_start": 1270,
          "aa_end": null,
          "aa_length": 1962,
          "cds_start": 3810,
          "cds_end": null,
          "cds_length": 5889,
          "cdna_start": 4145,
          "cdna_end": null,
          "cdna_length": 6983,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 35,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "c.3810A>G",
          "hgvs_p": "p.Glu1270Glu",
          "transcript": "ENST00000373957.7",
          "protein_id": "ENSP00000363068.4",
          "transcript_support_level": 5,
          "aa_start": 1270,
          "aa_end": null,
          "aa_length": 1962,
          "cds_start": 3810,
          "cds_end": null,
          "cds_length": 5889,
          "cdna_start": 4205,
          "cdna_end": null,
          "cdna_length": 7032,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 34,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "c.3795A>G",
          "hgvs_p": "p.Glu1265Glu",
          "transcript": "NM_001142764.2",
          "protein_id": "NP_001136236.1",
          "transcript_support_level": null,
          "aa_start": 1265,
          "aa_end": null,
          "aa_length": 1957,
          "cds_start": 3795,
          "cds_end": null,
          "cds_length": 5874,
          "cdna_start": 4130,
          "cdna_end": null,
          "cdna_length": 6968,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 34,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "c.3795A>G",
          "hgvs_p": "p.Glu1265Glu",
          "transcript": "ENST00000361849.7",
          "protein_id": "ENSP00000354950.3",
          "transcript_support_level": 5,
          "aa_start": 1265,
          "aa_end": null,
          "aa_length": 1957,
          "cds_start": 3795,
          "cds_end": null,
          "cds_length": 5874,
          "cdna_start": 4190,
          "cdna_end": null,
          "cdna_length": 7017,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 28,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "c.3795A>G",
          "hgvs_p": "p.Glu1265Glu",
          "transcript": "NM_001142766.2",
          "protein_id": "NP_001136238.1",
          "transcript_support_level": null,
          "aa_start": 1265,
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          "aa_length": 1952,
          "cds_start": 3795,
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          "cdna_start": 4130,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 28,
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          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "c.3795A>G",
          "hgvs_p": "p.Glu1265Glu",
          "transcript": "ENST00000395430.5",
          "protein_id": "ENSP00000378818.1",
          "transcript_support_level": 5,
          "aa_start": 1265,
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          "aa_length": 1952,
          "cds_start": 3795,
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          "cdna_start": 4190,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 27,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "c.3729A>G",
          "hgvs_p": "p.Glu1243Glu",
          "transcript": "NM_001142768.2",
          "protein_id": "NP_001136240.1",
          "transcript_support_level": null,
          "aa_start": 1243,
          "aa_end": null,
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          "cds_start": 3729,
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          "cdna_start": 4064,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
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          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
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          "intron_rank": null,
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          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "c.3729A>G",
          "hgvs_p": "p.Glu1243Glu",
          "transcript": "NM_001354404.2",
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 27,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "c.3729A>G",
          "hgvs_p": "p.Glu1243Glu",
          "transcript": "NM_001142773.2",
          "protein_id": "NP_001136245.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 1932,
          "cds_start": 3729,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 27,
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          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "c.3729A>G",
          "hgvs_p": "p.Glu1243Glu",
          "transcript": "ENST00000395433.5",
          "protein_id": "ENSP00000378821.1",
          "transcript_support_level": 5,
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          "aa_length": 1932,
          "cds_start": 3729,
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 27,
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          "exon_count": 31,
          "intron_rank": null,
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          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "c.3684A>G",
          "hgvs_p": "p.Glu1228Glu",
          "transcript": "NM_001142767.2",
          "protein_id": "NP_001136239.1",
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        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 26,
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          "intron_rank": null,
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          "gene_symbol": "PCDH15",
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          "hgvs_c": "c.3582A>G",
          "hgvs_p": "p.Glu1194Glu",
          "transcript": "NM_001142765.2",
          "protein_id": "NP_001136237.1",
          "transcript_support_level": null,
          "aa_start": 1194,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 26,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PCDH15",
          "gene_hgnc_id": 14674,
          "hgvs_c": "c.3582A>G",
          "hgvs_p": "p.Glu1194Glu",
          "transcript": "ENST00000437009.5",
          "protein_id": "ENSP00000412628.2",
          "transcript_support_level": 5,
          "aa_start": 1194,
          "aa_end": null,
          "aa_length": 1886,
          "cds_start": 3582,
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          "cdna_start": 3977,
          "cdna_end": null,
          "cdna_length": 6804,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "E",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
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      "gene_symbol": "PCDH15",
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      "dbsnp": "rs111033496",
      "frequency_reference_population": 6.9184523e-7,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 1,
      "gnomad_exomes_af": 6.91845e-7,
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      "gnomad_exomes_ac": 1,
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      "gnomad_exomes_homalt": 0,
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      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.5099999904632568,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.09000000357627869,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
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      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.51,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.019,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.09,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
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      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -3,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong,BP7",
      "acmg_by_gene": [
        {
          "score": -3,
          "benign_score": 5,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP7"
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          "verdict": "Likely_benign",
          "transcript": "ENST00000644397.2",
          "gene_symbol": "PCDH15",
          "hgnc_id": 14674,
          "effects": [
            "synonymous_variant"
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          "inheritance_mode": "AR",
          "hgvs_c": "c.3795A>G",
          "hgvs_p": "p.Glu1265Glu"
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      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}