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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: 8-143920743-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=143920743&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 17,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BP7",
            "BS1"
          ],
          "effects": [
            "synonymous_variant"
          ],
          "gene_symbol": "PLEC",
          "hgnc_id": 9069,
          "hgvs_c": "c.9489C>T",
          "hgvs_p": "p.Ile3163Ile",
          "inheritance_mode": "AR,AD",
          "pathogenic_score": 0,
          "score": -17,
          "transcript": "NM_201380.4",
          "verdict": "Benign"
        }
      ],
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BP7,BS1",
      "acmg_score": -17,
      "allele_count_reference_population": 161,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "A",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Benign",
      "bayesdelnoaf_score": -0.77,
      "chr": "8",
      "clinvar_classification": "Likely benign",
      "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,PLEC-related disorder",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "computational_prediction_selected": "Benign",
      "computational_score_selected": -0.7699999809265137,
      "computational_source_selected": "BayesDel_noAF",
      "consequences": [
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 4547,
          "aa_ref": "I",
          "aa_start": 3026,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14804,
          "cdna_start": 9214,
          "cds_end": null,
          "cds_length": 13644,
          "cds_start": 9078,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 32,
          "exon_rank_end": null,
          "feature": "NM_201384.3",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.9078C>T",
          "hgvs_p": "p.Ile3026Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000345136.8",
          "protein_coding": true,
          "protein_id": "NP_958786.1",
          "strand": false,
          "transcript": "NM_201384.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 4547,
          "aa_ref": "I",
          "aa_start": 3026,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 14804,
          "cdna_start": 9214,
          "cds_end": null,
          "cds_length": 13644,
          "cds_start": 9078,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 32,
          "exon_rank_end": null,
          "feature": "ENST00000345136.8",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.9078C>T",
          "hgvs_p": "p.Ile3026Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_201384.3",
          "protein_coding": true,
          "protein_id": "ENSP00000344848.3",
          "strand": false,
          "transcript": "ENST00000345136.8",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 4533,
          "aa_ref": "I",
          "aa_start": 3012,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14683,
          "cdna_start": 9093,
          "cds_end": null,
          "cds_length": 13602,
          "cds_start": 9036,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 32,
          "exon_rank_end": null,
          "feature": "NM_201378.4",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.9036C>T",
          "hgvs_p": "p.Ile3012Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": "ENST00000356346.7",
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_958780.1",
          "strand": false,
          "transcript": "NM_201378.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 4533,
          "aa_ref": "I",
          "aa_start": 3012,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14683,
          "cdna_start": 9093,
          "cds_end": null,
          "cds_length": 13602,
          "cds_start": 9036,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 32,
          "exon_rank_end": null,
          "feature": "ENST00000356346.7",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.9036C>T",
          "hgvs_p": "p.Ile3012Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": "NM_201378.4",
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000348702.3",
          "strand": false,
          "transcript": "ENST00000356346.7",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 4684,
          "aa_ref": "I",
          "aa_start": 3163,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 15249,
          "cdna_start": 9659,
          "cds_end": null,
          "cds_length": 14055,
          "cds_start": 9489,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 32,
          "exon_rank_end": null,
          "feature": "ENST00000322810.8",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.9489C>T",
          "hgvs_p": "p.Ile3163Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000323856.4",
          "strand": false,
          "transcript": "ENST00000322810.8",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 4574,
          "aa_ref": "I",
          "aa_start": 3053,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14787,
          "cdna_start": 9197,
          "cds_end": null,
          "cds_length": 13725,
          "cds_start": 9159,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 33,
          "exon_rank": 33,
          "exon_rank_end": null,
          "feature": "ENST00000436759.6",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.9159C>T",
          "hgvs_p": "p.Ile3053Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000388180.2",
          "strand": false,
          "transcript": "ENST00000436759.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 4551,
          "aa_ref": "I",
          "aa_start": 3030,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14689,
          "cdna_start": 9099,
          "cds_end": null,
          "cds_length": 13656,
          "cds_start": 9090,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 32,
          "exon_rank_end": null,
          "feature": "ENST00000357649.6",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.9090C>T",
          "hgvs_p": "p.Ile3030Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000350277.2",
          "strand": false,
          "transcript": "ENST00000357649.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 4547,
          "aa_ref": "I",
          "aa_start": 3026,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14736,
          "cdna_start": 9146,
          "cds_end": null,
          "cds_length": 13644,
          "cds_start": 9078,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 32,
          "exon_rank_end": null,
          "feature": "ENST00000354589.7",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.9078C>T",
          "hgvs_p": "p.Ile3026Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000346602.3",
          "strand": false,
          "transcript": "ENST00000354589.7",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 4525,
          "aa_ref": "I",
          "aa_start": 3004,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14751,
          "cdna_start": 9161,
          "cds_end": null,
          "cds_length": 13578,
          "cds_start": 9012,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 32,
          "exon_rank_end": null,
          "feature": "ENST00000354958.6",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.9012C>T",
          "hgvs_p": "p.Ile3004Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000347044.2",
          "strand": false,
          "transcript": "ENST00000354958.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 4515,
          "aa_ref": "I",
          "aa_start": 2994,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14646,
          "cdna_start": 9056,
          "cds_end": null,
          "cds_length": 13548,
          "cds_start": 8982,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 32,
          "exon_rank_end": null,
          "feature": "ENST00000398774.6",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.8982C>T",
          "hgvs_p": "p.Ile2994Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000381756.2",
          "strand": false,
          "transcript": "ENST00000398774.6",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 4684,
          "aa_ref": "I",
          "aa_start": 3163,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 15299,
          "cdna_start": 9709,
          "cds_end": null,
          "cds_length": 14055,
          "cds_start": 9489,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 32,
          "exon_rank_end": null,
          "feature": "NM_201380.4",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.9489C>T",
          "hgvs_p": "p.Ile3163Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_958782.1",
          "strand": false,
          "transcript": "NM_201380.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 4591,
          "aa_ref": "I",
          "aa_start": 3070,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 13782,
          "cdna_start": 9216,
          "cds_end": null,
          "cds_length": 13776,
          "cds_start": 9210,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 34,
          "exon_rank": 34,
          "exon_rank_end": null,
          "feature": "ENST00000528025.6",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.9210C>T",
          "hgvs_p": "p.Ile3070Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000437303.2",
          "strand": false,
          "transcript": "ENST00000528025.6",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 4574,
          "aa_ref": "I",
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          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14798,
          "cdna_start": 9208,
          "cds_end": null,
          "cds_length": 13725,
          "cds_start": 9159,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 33,
          "exon_rank": 33,
          "exon_rank_end": null,
          "feature": "NM_000445.5",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.9159C>T",
          "hgvs_p": "p.Ile3053Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_000436.2",
          "strand": false,
          "transcript": "NM_000445.5",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
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          "aa_length": 4570,
          "aa_ref": "I",
          "aa_start": 3049,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 13713,
          "cdna_start": 9147,
          "cds_end": null,
          "cds_length": 13713,
          "cds_start": 9147,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 32,
          "exon_rank_end": null,
          "feature": "ENST00000527096.5",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.9147C>T",
          "hgvs_p": "p.Ile3049Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000434583.1",
          "strand": false,
          "transcript": "ENST00000527096.5",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "I",
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          "aa_length": 4564,
          "aa_ref": "I",
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          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 13737,
          "cdna_start": 9171,
          "cds_end": null,
          "cds_length": 13695,
          "cds_start": 9129,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 32,
          "exon_rank_end": null,
          "feature": "ENST00000685198.1",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.9129C>T",
          "hgvs_p": "p.Ile3043Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000510528.1",
          "strand": false,
          "transcript": "ENST00000685198.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 4551,
          "aa_ref": "I",
          "aa_start": 3030,
          "biotype": "protein_coding",
          "canonical": false,
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          "cdna_length": 14789,
          "cdna_start": 9199,
          "cds_end": null,
          "cds_length": 13656,
          "cds_start": 9090,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 32,
          "exon_rank_end": null,
          "feature": "NM_201383.3",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.9090C>T",
          "hgvs_p": "p.Ile3030Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_958785.1",
          "strand": false,
          "transcript": "NM_201383.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
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          "aa_length": 4547,
          "aa_ref": "I",
          "aa_start": 3026,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14763,
          "cdna_start": 9173,
          "cds_end": null,
          "cds_length": 13644,
          "cds_start": 9078,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 32,
          "exon_rank_end": null,
          "feature": "NM_201382.4",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.9078C>T",
          "hgvs_p": "p.Ile3026Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_958784.1",
          "strand": false,
          "transcript": "NM_201382.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
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          "aa_length": 4525,
          "aa_ref": "I",
          "aa_start": 3004,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 14665,
          "cdna_start": 9075,
          "cds_end": null,
          "cds_length": 13578,
          "cds_start": 9012,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_count": 32,
          "exon_rank": 32,
          "exon_rank_end": null,
          "feature": "NM_201379.3",
          "gene_hgnc_id": 9069,
          "gene_symbol": "PLEC",
          "hgvs_c": "c.9012C>T",
          "hgvs_p": "p.Ile3004Ile",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_958781.1",
          "strand": false,
          "transcript": "NM_201379.3",
          "transcript_support_level": null
        },
        {
          "aa_alt": "I",
          "aa_end": null,
          "aa_length": 4524,
          "aa_ref": "I",
          "aa_start": 3003,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 13588,
          "cdna_start": 9022,
          "cds_end": null,
          "cds_length": 13575,
          "cds_start": 9009,
          "consequences": [
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        {
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            "intron_variant"
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          "feature": "ENST00000915283.1",
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          "protein_coding": true,
          "protein_id": "ENSP00000585342.1",
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          "transcript": "ENST00000915283.1",
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        }
      ],
      "custom_annotations": null,
      "dbscsnv_ada_prediction": null,
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      "dbsnp": "rs201586456",
      "effect": "synonymous_variant",
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      "gnomad_exomes_ac": 99,
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      "pathogenicity_classification_combined": "Likely benign",
      "phenotype_combined": "Epidermolysis bullosa simplex with nail dystrophy;Epidermolysis bullosa simplex, Ogna type;Autosomal recessive limb-girdle muscular dystrophy type 2Q;Epidermolysis bullosa simplex 5B, with muscular dystrophy;Epidermolysis bullosa simplex 5C, with pyloric atresia|PLEC-related disorder",
      "phylop100way_prediction": "Benign",
      "phylop100way_score": -1.338,
      "pos": 143920743,
      "ref": "G",
      "revel_prediction": null,
      "revel_score": null,
      "splice_prediction_selected": "Benign",
      "splice_score_selected": 0,
      "splice_source_selected": "max_spliceai",
      "spliceai_max_prediction": "Benign",
      "spliceai_max_score": 0,
      "transcript": "NM_201380.4"
    }
  ]
}
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