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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: 22-31846908-A-G (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=22&pos=31846908&ref=A&alt=G&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "22",
      "pos": 31846908,
      "ref": "A",
      "alt": "G",
      "effect": "synonymous_variant",
      "transcript": "ENST00000651528.2",
      "consequences": [
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 43,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "c.3096A>G",
          "hgvs_p": "p.Pro1032Pro",
          "transcript": "NM_001242896.3",
          "protein_id": "NP_001229825.1",
          "transcript_support_level": null,
          "aa_start": 1032,
          "aa_end": null,
          "aa_length": 1603,
          "cds_start": 3096,
          "cds_end": null,
          "cds_length": 4812,
          "cdna_start": 3302,
          "cdna_end": null,
          "cdna_length": 6554,
          "mane_select": "ENST00000651528.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 43,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "c.3096A>G",
          "hgvs_p": "p.Pro1032Pro",
          "transcript": "ENST00000651528.2",
          "protein_id": "ENSP00000498382.1",
          "transcript_support_level": null,
          "aa_start": 1032,
          "aa_end": null,
          "aa_length": 1603,
          "cds_start": 3096,
          "cds_end": null,
          "cds_length": 4812,
          "cdna_start": 3302,
          "cdna_end": null,
          "cdna_length": 6554,
          "mane_select": "NM_001242896.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 43,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "c.3096A>G",
          "hgvs_p": "p.Pro1032Pro",
          "transcript": "ENST00000382112.8",
          "protein_id": "ENSP00000371546.4",
          "transcript_support_level": 1,
          "aa_start": 1032,
          "aa_end": null,
          "aa_length": 1603,
          "cds_start": 3096,
          "cds_end": null,
          "cds_length": 4812,
          "cdna_start": 3182,
          "cdna_end": null,
          "cdna_length": 5390,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "c.3012A>G",
          "hgvs_p": "p.Pro1004Pro",
          "transcript": "ENST00000433147.2",
          "protein_id": "ENSP00000410544.2",
          "transcript_support_level": 1,
          "aa_start": 1004,
          "aa_end": null,
          "aa_length": 1575,
          "cds_start": 3012,
          "cds_end": null,
          "cds_length": 4728,
          "cdna_start": 3114,
          "cdna_end": null,
          "cdna_length": 5331,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "c.3069A>G",
          "hgvs_p": "p.Pro1023Pro",
          "transcript": "ENST00000400248.7",
          "protein_id": "ENSP00000383107.1",
          "transcript_support_level": 1,
          "aa_start": 1023,
          "aa_end": null,
          "aa_length": 1572,
          "cds_start": 3069,
          "cds_end": null,
          "cds_length": 4719,
          "cdna_start": 3152,
          "cdna_end": null,
          "cdna_length": 5319,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 29,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "n.2862A>G",
          "hgvs_p": null,
          "transcript": "ENST00000400246.7",
          "protein_id": "ENSP00000383105.3",
          "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": 5725,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "n.1152A>G",
          "hgvs_p": null,
          "transcript": "ENST00000448753.6",
          "protein_id": "ENSP00000402173.1",
          "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": 3256,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": 20,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000285404",
          "gene_hgnc_id": null,
          "hgvs_c": "c.1786+27683A>G",
          "hgvs_p": null,
          "transcript": "ENST00000646701.1",
          "protein_id": "ENSP00000496158.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 600,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1803,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1914,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 43,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "c.3096A>G",
          "hgvs_p": "p.Pro1032Pro",
          "transcript": "NM_001364318.2",
          "protein_id": "NP_001351247.1",
          "transcript_support_level": null,
          "aa_start": 1032,
          "aa_end": null,
          "aa_length": 1603,
          "cds_start": 3096,
          "cds_end": null,
          "cds_length": 4812,
          "cdna_start": 3185,
          "cdna_end": null,
          "cdna_length": 6437,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 43,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "c.3069A>G",
          "hgvs_p": "p.Pro1023Pro",
          "transcript": "NM_001136029.4",
          "protein_id": "NP_001129501.1",
          "transcript_support_level": null,
          "aa_start": 1023,
          "aa_end": null,
          "aa_length": 1594,
          "cds_start": 3069,
          "cds_end": null,
          "cds_length": 4785,
          "cdna_start": 3158,
          "cdna_end": null,
          "cdna_length": 6410,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 43,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "c.3069A>G",
          "hgvs_p": "p.Pro1023Pro",
          "transcript": "ENST00000645711.1",
          "protein_id": "ENSP00000493489.1",
          "transcript_support_level": null,
          "aa_start": 1023,
          "aa_end": null,
          "aa_length": 1594,
          "cds_start": 3069,
          "cds_end": null,
          "cds_length": 4785,
          "cdna_start": 3226,
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          "cdna_length": 5450,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "c.3120A>G",
          "hgvs_p": "p.Pro1040Pro",
          "transcript": "ENST00000645407.1",
          "protein_id": "ENSP00000496252.1",
          "transcript_support_level": null,
          "aa_start": 1040,
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          "aa_length": 1589,
          "cds_start": 3120,
          "cds_end": null,
          "cds_length": 4770,
          "cdna_start": 3127,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "c.3096A>G",
          "hgvs_p": "p.Pro1032Pro",
          "transcript": "NM_001363852.2",
          "protein_id": "NP_001350781.1",
          "transcript_support_level": null,
          "aa_start": 1032,
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          "aa_length": 1581,
          "cds_start": 3096,
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          "cds_length": 4746,
          "cdna_start": 3185,
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          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "c.3096A>G",
          "hgvs_p": "p.Pro1032Pro",
          "transcript": "NM_001364320.2",
          "protein_id": "NP_001351249.1",
          "transcript_support_level": null,
          "aa_start": 1032,
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          "aa_length": 1581,
          "cds_start": 3096,
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          "cdna_start": 3302,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
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          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
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          "intron_rank": null,
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          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "c.3096A>G",
          "hgvs_p": "p.Pro1032Pro",
          "transcript": "ENST00000400249.7",
          "protein_id": "ENSP00000383108.3",
          "transcript_support_level": 5,
          "aa_start": 1032,
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          "aa_length": 1581,
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          "cdna_start": 3188,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "c.3096A>G",
          "hgvs_p": "p.Pro1032Pro",
          "transcript": "ENST00000644331.1",
          "protein_id": "ENSP00000494406.1",
          "transcript_support_level": null,
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          "aa_length": 1581,
          "cds_start": 3096,
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          "cdna_length": 5383,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "c.3012A>G",
          "hgvs_p": "p.Pro1004Pro",
          "transcript": "NM_001369901.1",
          "protein_id": "NP_001356830.1",
          "transcript_support_level": null,
          "aa_start": 1004,
          "aa_end": null,
          "aa_length": 1575,
          "cds_start": 3012,
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          "cds_length": 4728,
          "cdna_start": 3214,
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          "cdna_length": 5448,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "c.3012A>G",
          "hgvs_p": "p.Pro1004Pro",
          "transcript": "NM_001369902.1",
          "protein_id": "NP_001356831.1",
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        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "c.3069A>G",
          "hgvs_p": "p.Pro1023Pro",
          "transcript": "NM_001369903.1",
          "protein_id": "NP_001356832.1",
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          "aa_length": 1572,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
          "exon_count": 42,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DEPDC5",
          "gene_hgnc_id": 18423,
          "hgvs_c": "c.3069A>G",
          "hgvs_p": "p.Pro1023Pro",
          "transcript": "NM_014662.6",
          "protein_id": "NP_055477.1",
          "transcript_support_level": null,
          "aa_start": 1023,
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          "cds_start": 3069,
          "cds_end": null,
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          "cdna_start": 3158,
          "cdna_end": null,
          "cdna_length": 6344,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 31,
          "exon_rank_end": null,
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      ],
      "gene_symbol": "DEPDC5",
      "gene_hgnc_id": 18423,
      "dbsnp": "rs756207564",
      "frequency_reference_population": 0.000004956359,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 8,
      "gnomad_exomes_af": 0.00000410428,
      "gnomad_genomes_af": 0.0000131408,
      "gnomad_exomes_ac": 6,
      "gnomad_genomes_ac": 2,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.06499999761581421,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "REVEL",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.065,
      "revel_prediction": "Benign",
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.95,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -5.706,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -9,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Moderate,BP6_Moderate,BP7,BS2",
      "acmg_by_gene": [
        {
          "score": -9,
          "benign_score": 9,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Moderate",
            "BP6_Moderate",
            "BP7",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000651528.2",
          "gene_symbol": "DEPDC5",
          "hgnc_id": 18423,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.3096A>G",
          "hgvs_p": "p.Pro1032Pro"
        },
        {
          "score": -2,
          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate",
            "BP6_Moderate"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000646701.1",
          "gene_symbol": "ENSG00000285404",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "c.1786+27683A>G",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "DEPDC5-related disorder,Familial focal epilepsy with variable foci",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "Familial focal epilepsy with variable foci|DEPDC5-related disorder",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}