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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: 20-8421069-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=20&pos=8421069&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "20",
      "pos": 8421069,
      "ref": "C",
      "alt": "T",
      "effect": "intron_variant",
      "transcript": "NM_015192.4",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PLCB1",
          "gene_hgnc_id": 15917,
          "hgvs_c": "c.246+49619C>T",
          "hgvs_p": null,
          "transcript": "NM_015192.4",
          "protein_id": "NP_056007.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1216,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3651,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7088,
          "mane_select": "ENST00000338037.11",
          "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": 32,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PLCB1",
          "gene_hgnc_id": 15917,
          "hgvs_c": "c.246+49619C>T",
          "hgvs_p": null,
          "transcript": "ENST00000338037.11",
          "protein_id": "ENSP00000338185.6",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1216,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3651,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7088,
          "mane_select": "NM_015192.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PLCB1",
          "gene_hgnc_id": 15917,
          "hgvs_c": "c.246+49619C>T",
          "hgvs_p": null,
          "transcript": "ENST00000378637.6",
          "protein_id": "ENSP00000367904.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1173,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3522,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3864,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PLCB1",
          "gene_hgnc_id": 15917,
          "hgvs_c": "c.246+49619C>T",
          "hgvs_p": null,
          "transcript": "ENST00000378641.7",
          "protein_id": "ENSP00000367908.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1173,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3522,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7323,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PLCB1",
          "gene_hgnc_id": 15917,
          "hgvs_c": "c.246+49619C>T",
          "hgvs_p": null,
          "transcript": "ENST00000629992.2",
          "protein_id": "ENSP00000486531.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 248,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 747,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3095,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PLCB1",
          "gene_hgnc_id": 15917,
          "hgvs_c": "c.246+49619C>T",
          "hgvs_p": null,
          "transcript": "NM_182734.3",
          "protein_id": "NP_877398.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1173,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3522,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 7206,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PLCB1",
          "gene_hgnc_id": 15917,
          "hgvs_c": "c.-58+49619C>T",
          "hgvs_p": null,
          "transcript": "ENST00000637919.1",
          "protein_id": "ENSP00000490862.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1072,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3219,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5074,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 28,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PLCB1",
          "gene_hgnc_id": 15917,
          "hgvs_c": "c.-58+49619C>T",
          "hgvs_p": null,
          "transcript": "ENST00000625874.2",
          "protein_id": "ENSP00000486301.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 959,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 2881,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3206,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PLCB1",
          "gene_hgnc_id": 15917,
          "hgvs_c": "c.246+49619C>T",
          "hgvs_p": null,
          "transcript": "ENST00000404098.6",
          "protein_id": "ENSP00000384001.3",
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 205,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 618,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1260,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "PLCB1",
          "gene_hgnc_id": 15917,
          "hgvs_c": "c.-58+49619C>T",
          "hgvs_p": null,
          "transcript": "ENST00000630495.2",
          "protein_id": "ENSP00000486655.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 135,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 410,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 759,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PLCB1",
          "gene_hgnc_id": 15917,
          "hgvs_c": "n.371+49619C>T",
          "hgvs_p": null,
          "transcript": "ENST00000626114.2",
          "protein_id": null,
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 598,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PLCB1",
          "gene_hgnc_id": 15917,
          "hgvs_c": "n.382+49619C>T",
          "hgvs_p": null,
          "transcript": "ENST00000626161.1",
          "protein_id": null,
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 706,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PLCB1",
          "gene_hgnc_id": 15917,
          "hgvs_c": "n.317+49619C>T",
          "hgvs_p": null,
          "transcript": "ENST00000635830.1",
          "protein_id": null,
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3237,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "PLCB1",
          "gene_hgnc_id": 15917,
          "hgvs_c": "n.246+49619C>T",
          "hgvs_p": null,
          "transcript": "ENST00000636319.1",
          "protein_id": "ENSP00000490455.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2930,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PLCB1",
          "gene_hgnc_id": 15917,
          "hgvs_c": "n.81+49619C>T",
          "hgvs_p": null,
          "transcript": "ENST00000636784.1",
          "protein_id": null,
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 100,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PLCB1",
          "gene_hgnc_id": 15917,
          "hgvs_c": "n.110+49619C>T",
          "hgvs_p": null,
          "transcript": "ENST00000636825.1",
          "protein_id": null,
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3020,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "LOC124900459",
          "gene_hgnc_id": null,
          "hgvs_c": "n.6108-1273C>T",
          "hgvs_p": null,
          "transcript": "XR_007067518.1",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 96271,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "PLCB1",
      "gene_hgnc_id": 15917,
      "dbsnp": "rs708914",
      "frequency_reference_population": 0.453599,
      "hom_count_reference_population": 15780,
      "allele_count_reference_population": 68928,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": 0.453599,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": 68928,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": 15780,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.9300000071525574,
      "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": -0.93,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -1.849,
      "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": -12,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BA1",
      "acmg_by_gene": [
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "NM_015192.4",
          "gene_symbol": "PLCB1",
          "hgnc_id": 15917,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.246+49619C>T",
          "hgvs_p": null
        },
        {
          "score": -12,
          "benign_score": 12,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BA1"
          ],
          "verdict": "Benign",
          "transcript": "XR_007067518.1",
          "gene_symbol": "LOC124900459",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.6108-1273C>T",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}