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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: 15-49934162-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=49934162&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "15",
      "pos": 49934162,
      "ref": "G",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "NM_024837.4",
      "consequences": [
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "c.1308C>T",
          "hgvs_p": "p.Phe436Phe",
          "transcript": "NM_024837.4",
          "protein_id": "NP_079113.2",
          "transcript_support_level": null,
          "aa_start": 436,
          "aa_end": null,
          "aa_length": 1192,
          "cds_start": 1308,
          "cds_end": null,
          "cds_length": 3579,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000284509.11",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_024837.4"
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "c.1308C>T",
          "hgvs_p": "p.Phe436Phe",
          "transcript": "ENST00000284509.11",
          "protein_id": "ENSP00000284509.6",
          "transcript_support_level": 5,
          "aa_start": 436,
          "aa_end": null,
          "aa_length": 1192,
          "cds_start": 1308,
          "cds_end": null,
          "cds_length": 3579,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_024837.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000284509.11"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "n.1308C>T",
          "hgvs_p": null,
          "transcript": "ENST00000557955.5",
          "protein_id": "ENSP00000453690.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000557955.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "n.*1027C>T",
          "hgvs_p": null,
          "transcript": "ENST00000558906.5",
          "protein_id": "ENSP00000452956.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000558906.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "n.*1027C>T",
          "hgvs_p": null,
          "transcript": "ENST00000559726.5",
          "protein_id": "ENSP00000453229.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000559726.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "n.*1027C>T",
          "hgvs_p": null,
          "transcript": "ENST00000558906.5",
          "protein_id": "ENSP00000452956.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000558906.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "n.*1027C>T",
          "hgvs_p": null,
          "transcript": "ENST00000559726.5",
          "protein_id": "ENSP00000453229.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000559726.5"
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "c.1308C>T",
          "hgvs_p": "p.Phe436Phe",
          "transcript": "ENST00000559829.5",
          "protein_id": "ENSP00000453169.1",
          "transcript_support_level": 5,
          "aa_start": 436,
          "aa_end": null,
          "aa_length": 1192,
          "cds_start": 1308,
          "cds_end": null,
          "cds_length": 3579,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000559829.5"
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "c.1308C>T",
          "hgvs_p": "p.Phe436Phe",
          "transcript": "ENST00000895127.1",
          "protein_id": "ENSP00000565186.1",
          "transcript_support_level": null,
          "aa_start": 436,
          "aa_end": null,
          "aa_length": 1192,
          "cds_start": 1308,
          "cds_end": null,
          "cds_length": 3579,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000895127.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "c.1308C>T",
          "hgvs_p": "p.Phe436Phe",
          "transcript": "ENST00000895129.1",
          "protein_id": "ENSP00000565188.1",
          "transcript_support_level": null,
          "aa_start": 436,
          "aa_end": null,
          "aa_length": 1192,
          "cds_start": 1308,
          "cds_end": null,
          "cds_length": 3579,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000895129.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "c.1308C>T",
          "hgvs_p": "p.Phe436Phe",
          "transcript": "ENST00000895131.1",
          "protein_id": "ENSP00000565190.1",
          "transcript_support_level": null,
          "aa_start": 436,
          "aa_end": null,
          "aa_length": 1192,
          "cds_start": 1308,
          "cds_end": null,
          "cds_length": 3579,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000895131.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "c.1308C>T",
          "hgvs_p": "p.Phe436Phe",
          "transcript": "ENST00000895132.1",
          "protein_id": "ENSP00000565191.1",
          "transcript_support_level": null,
          "aa_start": 436,
          "aa_end": null,
          "aa_length": 1192,
          "cds_start": 1308,
          "cds_end": null,
          "cds_length": 3579,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000895132.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "c.1206C>T",
          "hgvs_p": "p.Phe402Phe",
          "transcript": "ENST00000966552.1",
          "protein_id": "ENSP00000636611.1",
          "transcript_support_level": null,
          "aa_start": 402,
          "aa_end": null,
          "aa_length": 1158,
          "cds_start": 1206,
          "cds_end": null,
          "cds_length": 3477,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000966552.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "c.1194C>T",
          "hgvs_p": "p.Phe398Phe",
          "transcript": "ENST00000966553.1",
          "protein_id": "ENSP00000636612.1",
          "transcript_support_level": null,
          "aa_start": 398,
          "aa_end": null,
          "aa_length": 1154,
          "cds_start": 1194,
          "cds_end": null,
          "cds_length": 3465,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000966553.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "c.1308C>T",
          "hgvs_p": "p.Phe436Phe",
          "transcript": "ENST00000895128.1",
          "protein_id": "ENSP00000565187.1",
          "transcript_support_level": null,
          "aa_start": 436,
          "aa_end": null,
          "aa_length": 1129,
          "cds_start": 1308,
          "cds_end": null,
          "cds_length": 3390,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000895128.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 15,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "c.1308C>T",
          "hgvs_p": "p.Phe436Phe",
          "transcript": "ENST00000895130.1",
          "protein_id": "ENSP00000565189.1",
          "transcript_support_level": null,
          "aa_start": 436,
          "aa_end": null,
          "aa_length": 1129,
          "cds_start": 1308,
          "cds_end": null,
          "cds_length": 3390,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000895130.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "c.1503C>T",
          "hgvs_p": "p.Phe501Phe",
          "transcript": "XM_011522046.3",
          "protein_id": "XP_011520348.1",
          "transcript_support_level": null,
          "aa_start": 501,
          "aa_end": null,
          "aa_length": 1257,
          "cds_start": 1503,
          "cds_end": null,
          "cds_length": 3774,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_011522046.3"
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "c.1419C>T",
          "hgvs_p": "p.Phe473Phe",
          "transcript": "XM_024450065.2",
          "protein_id": "XP_024305833.1",
          "transcript_support_level": null,
          "aa_start": 473,
          "aa_end": null,
          "aa_length": 1229,
          "cds_start": 1419,
          "cds_end": null,
          "cds_length": 3690,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_024450065.2"
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "c.1392C>T",
          "hgvs_p": "p.Phe464Phe",
          "transcript": "XM_011522047.3",
          "protein_id": "XP_011520349.1",
          "transcript_support_level": null,
          "aa_start": 464,
          "aa_end": null,
          "aa_length": 1220,
          "cds_start": 1392,
          "cds_end": null,
          "cds_length": 3663,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_011522047.3"
        },
        {
          "aa_ref": "F",
          "aa_alt": "F",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 29,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "c.1392C>T",
          "hgvs_p": "p.Phe464Phe",
          "transcript": "XM_011522048.2",
          "protein_id": "XP_011520350.1",
          "transcript_support_level": null,
          "aa_start": 464,
          "aa_end": null,
          "aa_length": 1220,
          "cds_start": 1392,
          "cds_end": null,
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          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP8B4",
          "gene_hgnc_id": 13536,
          "hgvs_c": "n.1708C>T",
          "hgvs_p": null,
          "transcript": "XR_002957687.2",
          "protein_id": null,
          "transcript_support_level": null,
          "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": "pseudogene",
          "feature": "XR_002957687.2"
        }
      ],
      "gene_symbol": "ATP8B4",
      "gene_hgnc_id": 13536,
      "dbsnp": "rs55687265",
      "frequency_reference_population": 6.856115e-7,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 1,
      "gnomad_exomes_af": 6.85611e-7,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 1,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.46000000834465027,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.46,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 1.561,
      "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": -1,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Moderate,BP7",
      "acmg_by_gene": [
        {
          "score": -1,
          "benign_score": 3,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_024837.4",
          "gene_symbol": "ATP8B4",
          "hgnc_id": 13536,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.1308C>T",
          "hgvs_p": "p.Phe436Phe"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}