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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: 8-143916558-G-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=143916558&ref=G&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "8",
      "pos": 143916558,
      "ref": "G",
      "alt": "C",
      "effect": "synonymous_variant",
      "transcript": "NM_201380.4",
      "consequences": [
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.13263C>G",
          "hgvs_p": "p.Thr4421Thr",
          "transcript": "NM_201384.3",
          "protein_id": "NP_958786.1",
          "transcript_support_level": null,
          "aa_start": 4421,
          "aa_end": null,
          "aa_length": 4547,
          "cds_start": 13263,
          "cds_end": null,
          "cds_length": 13644,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000345136.8",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_201384.3"
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.13263C>G",
          "hgvs_p": "p.Thr4421Thr",
          "transcript": "ENST00000345136.8",
          "protein_id": "ENSP00000344848.3",
          "transcript_support_level": 1,
          "aa_start": 4421,
          "aa_end": null,
          "aa_length": 4547,
          "cds_start": 13263,
          "cds_end": null,
          "cds_length": 13644,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_201384.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000345136.8"
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.13221C>G",
          "hgvs_p": "p.Thr4407Thr",
          "transcript": "NM_201378.4",
          "protein_id": "NP_958780.1",
          "transcript_support_level": null,
          "aa_start": 4407,
          "aa_end": null,
          "aa_length": 4533,
          "cds_start": 13221,
          "cds_end": null,
          "cds_length": 13602,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": "ENST00000356346.7",
          "biotype": "protein_coding",
          "feature": "NM_201378.4"
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.13221C>G",
          "hgvs_p": "p.Thr4407Thr",
          "transcript": "ENST00000356346.7",
          "protein_id": "ENSP00000348702.3",
          "transcript_support_level": 1,
          "aa_start": 4407,
          "aa_end": null,
          "aa_length": 4533,
          "cds_start": 13221,
          "cds_end": null,
          "cds_length": 13602,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": "NM_201378.4",
          "biotype": "protein_coding",
          "feature": "ENST00000356346.7"
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.13674C>G",
          "hgvs_p": "p.Thr4558Thr",
          "transcript": "ENST00000322810.8",
          "protein_id": "ENSP00000323856.4",
          "transcript_support_level": 1,
          "aa_start": 4558,
          "aa_end": null,
          "aa_length": 4684,
          "cds_start": 13674,
          "cds_end": null,
          "cds_length": 14055,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000322810.8"
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 33,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.13344C>G",
          "hgvs_p": "p.Thr4448Thr",
          "transcript": "ENST00000436759.6",
          "protein_id": "ENSP00000388180.2",
          "transcript_support_level": 1,
          "aa_start": 4448,
          "aa_end": null,
          "aa_length": 4574,
          "cds_start": 13344,
          "cds_end": null,
          "cds_length": 13725,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000436759.6"
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.13275C>G",
          "hgvs_p": "p.Thr4425Thr",
          "transcript": "ENST00000357649.6",
          "protein_id": "ENSP00000350277.2",
          "transcript_support_level": 1,
          "aa_start": 4425,
          "aa_end": null,
          "aa_length": 4551,
          "cds_start": 13275,
          "cds_end": null,
          "cds_length": 13656,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000357649.6"
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.13263C>G",
          "hgvs_p": "p.Thr4421Thr",
          "transcript": "ENST00000354589.7",
          "protein_id": "ENSP00000346602.3",
          "transcript_support_level": 1,
          "aa_start": 4421,
          "aa_end": null,
          "aa_length": 4547,
          "cds_start": 13263,
          "cds_end": null,
          "cds_length": 13644,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000354589.7"
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.13197C>G",
          "hgvs_p": "p.Thr4399Thr",
          "transcript": "ENST00000354958.6",
          "protein_id": "ENSP00000347044.2",
          "transcript_support_level": 1,
          "aa_start": 4399,
          "aa_end": null,
          "aa_length": 4525,
          "cds_start": 13197,
          "cds_end": null,
          "cds_length": 13578,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000354958.6"
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.13167C>G",
          "hgvs_p": "p.Thr4389Thr",
          "transcript": "ENST00000398774.6",
          "protein_id": "ENSP00000381756.2",
          "transcript_support_level": 1,
          "aa_start": 4389,
          "aa_end": null,
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          "cds_start": 13167,
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          "cds_length": 13548,
          "cdna_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.13674C>G",
          "hgvs_p": "p.Thr4558Thr",
          "transcript": "NM_201380.4",
          "protein_id": "NP_958782.1",
          "transcript_support_level": null,
          "aa_start": 4558,
          "aa_end": null,
          "aa_length": 4684,
          "cds_start": 13674,
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          "cds_length": 14055,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_201380.4"
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 34,
          "exon_rank_end": null,
          "exon_count": 34,
          "intron_rank": null,
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          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.13395C>G",
          "hgvs_p": "p.Thr4465Thr",
          "transcript": "ENST00000528025.6",
          "protein_id": "ENSP00000437303.2",
          "transcript_support_level": 5,
          "aa_start": 4465,
          "aa_end": null,
          "aa_length": 4591,
          "cds_start": 13395,
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          "cdna_start": null,
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        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 33,
          "exon_rank_end": null,
          "exon_count": 33,
          "intron_rank": null,
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          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.13344C>G",
          "hgvs_p": "p.Thr4448Thr",
          "transcript": "NM_000445.5",
          "protein_id": "NP_000436.2",
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          "cdna_start": null,
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.13332C>G",
          "hgvs_p": "p.Thr4444Thr",
          "transcript": "ENST00000527096.5",
          "protein_id": "ENSP00000434583.1",
          "transcript_support_level": 5,
          "aa_start": 4444,
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        },
        {
          "aa_ref": "T",
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          "exon_count": 32,
          "intron_rank": null,
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          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
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          "transcript": "ENST00000685198.1",
          "protein_id": "ENSP00000510528.1",
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          "biotype": "protein_coding",
          "feature": "ENST00000685198.1"
        },
        {
          "aa_ref": "T",
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 32,
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          "intron_rank": null,
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          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.13275C>G",
          "hgvs_p": "p.Thr4425Thr",
          "transcript": "NM_201383.3",
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          "biotype": "protein_coding",
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        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
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          "protein_coding": true,
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          "consequences": [
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          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
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          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.13263C>G",
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          "transcript": "NM_201382.4",
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        {
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          ],
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        },
        {
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          "consequences": [
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          ],
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          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
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          "transcript": "ENST00000693060.1",
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          "biotype": "protein_coding",
          "feature": "ENST00000693060.1"
        },
        {
          "aa_ref": "T",
          "aa_alt": "T",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 32,
          "exon_rank_end": null,
          "exon_count": 32,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PLEC",
          "gene_hgnc_id": 9069,
          "hgvs_c": "c.13167C>G",
          "hgvs_p": "p.Thr4389Thr",
          "transcript": "NM_201381.3",
          "protein_id": "NP_958783.1",
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      "dbsnp": "rs369202116",
      "frequency_reference_population": 0.0000013704713,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 2,
      "gnomad_exomes_af": 0.00000137047,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 2,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.949999988079071,
      "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": -0.95,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -6.366,
      "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": -5,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong,BP6_Moderate,BP7",
      "acmg_by_gene": [
        {
          "score": -5,
          "benign_score": 7,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP6_Moderate",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_201380.4",
          "gene_symbol": "PLEC",
          "hgnc_id": 9069,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR,AD",
          "hgvs_c": "c.13674C>G",
          "hgvs_p": "p.Thr4558Thr"
        }
      ],
      "clinvar_disease": " Ogna type, with muscular dystrophy, with pyloric atresia,Autosomal recessive limb-girdle muscular dystrophy type 2Q,Epidermolysis bullosa simplex,Epidermolysis bullosa simplex 5B,Epidermolysis bullosa simplex 5C,Epidermolysis bullosa simplex with nail dystrophy",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "Epidermolysis bullosa simplex, Ogna type;Epidermolysis bullosa simplex 5B, with muscular dystrophy;Autosomal recessive limb-girdle muscular dystrophy type 2Q;Epidermolysis bullosa simplex with nail dystrophy;Epidermolysis bullosa simplex 5C, with pyloric atresia",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}
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