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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: 6-83171948-G-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=83171948&ref=G&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "6",
      "pos": 83171948,
      "ref": "G",
      "alt": "T",
      "effect": "missense_variant",
      "transcript": "ENST00000513973.6",
      "consequences": [
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PGM3",
          "gene_hgnc_id": 8907,
          "hgvs_c": "c.1354C>A",
          "hgvs_p": "p.Leu452Ile",
          "transcript": "NM_015599.3",
          "protein_id": "NP_056414.1",
          "transcript_support_level": null,
          "aa_start": 452,
          "aa_end": null,
          "aa_length": 542,
          "cds_start": 1354,
          "cds_end": null,
          "cds_length": 1629,
          "cdna_start": 1443,
          "cdna_end": null,
          "cdna_length": 6079,
          "mane_select": "ENST00000513973.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PGM3",
          "gene_hgnc_id": 8907,
          "hgvs_c": "c.1354C>A",
          "hgvs_p": "p.Leu452Ile",
          "transcript": "ENST00000513973.6",
          "protein_id": "ENSP00000424874.1",
          "transcript_support_level": 1,
          "aa_start": 452,
          "aa_end": null,
          "aa_length": 542,
          "cds_start": 1354,
          "cds_end": null,
          "cds_length": 1629,
          "cdna_start": 1443,
          "cdna_end": null,
          "cdna_length": 6079,
          "mane_select": "NM_015599.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PGM3",
          "gene_hgnc_id": 8907,
          "hgvs_c": "c.1354C>A",
          "hgvs_p": "p.Leu452Ile",
          "transcript": "ENST00000512866.5",
          "protein_id": "ENSP00000421565.1",
          "transcript_support_level": 1,
          "aa_start": 452,
          "aa_end": null,
          "aa_length": 566,
          "cds_start": 1354,
          "cds_end": null,
          "cds_length": 1701,
          "cdna_start": 1409,
          "cdna_end": null,
          "cdna_length": 2013,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PGM3",
          "gene_hgnc_id": 8907,
          "hgvs_c": "c.1111C>A",
          "hgvs_p": "p.Leu371Ile",
          "transcript": "ENST00000283977.9",
          "protein_id": "ENSP00000283977.5",
          "transcript_support_level": 5,
          "aa_start": 371,
          "aa_end": null,
          "aa_length": 441,
          "cds_start": 1111,
          "cds_end": null,
          "cds_length": 1326,
          "cdna_start": 1238,
          "cdna_end": null,
          "cdna_length": 2223,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PGM3",
          "gene_hgnc_id": 8907,
          "hgvs_c": "c.1438C>A",
          "hgvs_p": "p.Leu480Ile",
          "transcript": "NM_001199917.2",
          "protein_id": "NP_001186846.1",
          "transcript_support_level": null,
          "aa_start": 480,
          "aa_end": null,
          "aa_length": 570,
          "cds_start": 1438,
          "cds_end": null,
          "cds_length": 1713,
          "cdna_start": 1571,
          "cdna_end": null,
          "cdna_length": 6207,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PGM3",
          "gene_hgnc_id": 8907,
          "hgvs_c": "c.1438C>A",
          "hgvs_p": "p.Leu480Ile",
          "transcript": "NM_001367287.1",
          "protein_id": "NP_001354216.1",
          "transcript_support_level": null,
          "aa_start": 480,
          "aa_end": null,
          "aa_length": 570,
          "cds_start": 1438,
          "cds_end": null,
          "cds_length": 1713,
          "cdna_start": 1580,
          "cdna_end": null,
          "cdna_length": 6216,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PGM3",
          "gene_hgnc_id": 8907,
          "hgvs_c": "c.1438C>A",
          "hgvs_p": "p.Leu480Ile",
          "transcript": "ENST00000506587.5",
          "protein_id": "ENSP00000425809.1",
          "transcript_support_level": 2,
          "aa_start": 480,
          "aa_end": null,
          "aa_length": 570,
          "cds_start": 1438,
          "cds_end": null,
          "cds_length": 1713,
          "cdna_start": 1585,
          "cdna_end": null,
          "cdna_length": 1971,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PGM3",
          "gene_hgnc_id": 8907,
          "hgvs_c": "c.1438C>A",
          "hgvs_p": "p.Leu480Ile",
          "transcript": "ENST00000508748.6",
          "protein_id": "ENSP00000424865.2",
          "transcript_support_level": 5,
          "aa_start": 480,
          "aa_end": null,
          "aa_length": 570,
          "cds_start": 1438,
          "cds_end": null,
          "cds_length": 1713,
          "cdna_start": 1608,
          "cdna_end": null,
          "cdna_length": 4518,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PGM3",
          "gene_hgnc_id": 8907,
          "hgvs_c": "c.1354C>A",
          "hgvs_p": "p.Leu452Ile",
          "transcript": "NM_001199919.2",
          "protein_id": "NP_001186848.1",
          "transcript_support_level": null,
          "aa_start": 452,
          "aa_end": null,
          "aa_length": 566,
          "cds_start": 1354,
          "cds_end": null,
          "cds_length": 1701,
          "cdna_start": 1443,
          "cdna_end": null,
          "cdna_length": 2047,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PGM3",
          "gene_hgnc_id": 8907,
          "hgvs_c": "c.1354C>A",
          "hgvs_p": "p.Leu452Ile",
          "transcript": "ENST00000509219.2",
          "protein_id": "ENSP00000423389.2",
          "transcript_support_level": 5,
          "aa_start": 452,
          "aa_end": null,
          "aa_length": 566,
          "cds_start": 1354,
          "cds_end": null,
          "cds_length": 1701,
          "cdna_start": 1446,
          "cdna_end": null,
          "cdna_length": 1952,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "PGM3",
          "gene_hgnc_id": 8907,
          "hgvs_c": "c.1354C>A",
          "hgvs_p": "p.Leu452Ile",
          "transcript": "ENST00000652468.1",
          "protein_id": "ENSP00000499112.1",
          "transcript_support_level": null,
          "aa_start": 452,
          "aa_end": null,
          "aa_length": 566,
          "cds_start": 1354,
          "cds_end": null,
          "cds_length": 1701,
          "cdna_start": 1602,
          "cdna_end": null,
          "cdna_length": 2060,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "L",
          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
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          "gene_symbol": "PGM3",
          "gene_hgnc_id": 8907,
          "hgvs_c": "c.1354C>A",
          "hgvs_p": "p.Leu452Ile",
          "transcript": "ENST00000507554.2",
          "protein_id": "ENSP00000425558.2",
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          "cds_start": 1354,
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          "mane_select": null,
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        {
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          "strand": false,
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          ],
          "exon_rank": 11,
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          "intron_rank": null,
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          "gene_symbol": "PGM3",
          "gene_hgnc_id": 8907,
          "hgvs_c": "c.1354C>A",
          "hgvs_p": "p.Leu452Ile",
          "transcript": "ENST00000698526.1",
          "protein_id": "ENSP00000513775.1",
          "transcript_support_level": null,
          "aa_start": 452,
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          "cds_start": 1354,
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        },
        {
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          "protein_coding": true,
          "strand": false,
          "consequences": [
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          "exon_count": 12,
          "intron_rank": null,
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          "gene_symbol": "PGM3",
          "gene_hgnc_id": 8907,
          "hgvs_c": "c.1255C>A",
          "hgvs_p": "p.Leu419Ile",
          "transcript": "ENST00000652222.2",
          "protein_id": "ENSP00000499141.2",
          "transcript_support_level": null,
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          "aa_end": null,
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          "cds_start": 1255,
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        },
        {
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          "gene_symbol": "PGM3",
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          "hgvs_c": "c.1255C>A",
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          "feature": null
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        {
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          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 10,
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          "exon_count": 12,
          "intron_rank": null,
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          "gene_symbol": "PGM3",
          "gene_hgnc_id": 8907,
          "hgvs_c": "c.1111C>A",
          "hgvs_p": "p.Leu371Ile",
          "transcript": "ENST00000651425.1",
          "protein_id": "ENSP00000498986.1",
          "transcript_support_level": null,
          "aa_start": 371,
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          "cds_start": 1111,
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        {
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          "exon_count": 12,
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          "gene_symbol": "PGM3",
          "gene_hgnc_id": 8907,
          "hgvs_c": "c.1111C>A",
          "hgvs_p": "p.Leu371Ile",
          "transcript": "ENST00000698610.1",
          "protein_id": "ENSP00000513837.1",
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          "aa_length": 461,
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          "cdna_start": 1225,
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        },
        {
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          "gene_symbol": "PGM3",
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          "hgvs_c": "c.1111C>A",
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        },
        {
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          "intron_rank": null,
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          "gene_symbol": "PGM3",
          "gene_hgnc_id": 8907,
          "hgvs_c": "c.1012C>A",
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          "transcript": "ENST00000698608.1",
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        },
        {
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          ],
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          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PGM3",
          "gene_hgnc_id": 8907,
          "hgvs_c": "c.916C>A",
          "hgvs_p": "p.Leu306Ile",
          "transcript": "ENST00000698612.1",
          "protein_id": "ENSP00000513838.1",
          "transcript_support_level": null,
          "aa_start": 306,
          "aa_end": null,
          "aa_length": 396,
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          "cds_end": null,
          "cds_length": 1191,
          "cdna_start": 1005,
          "cdna_end": null,
          "cdna_length": 3910,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "aa_alt": "I",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
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      ],
      "gene_symbol": "PGM3",
      "gene_hgnc_id": 8907,
      "dbsnp": "rs201593125",
      "frequency_reference_population": 0.0007607359,
      "hom_count_reference_population": 4,
      "allele_count_reference_population": 1227,
      "gnomad_exomes_af": 0.000775015,
      "gnomad_genomes_af": 0.000623785,
      "gnomad_exomes_ac": 1132,
      "gnomad_genomes_ac": 95,
      "gnomad_exomes_homalt": 4,
      "gnomad_genomes_homalt": 0,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.04812580347061157,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.091,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.0854,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.45,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 5.337,
      "phylop100way_prediction": "Uncertain_significance",
      "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_Strong,BS1_Supporting,BS2",
      "acmg_by_gene": [
        {
          "score": -9,
          "benign_score": 9,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BS1_Supporting",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000513973.6",
          "gene_symbol": "PGM3",
          "hgnc_id": 8907,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.1354C>A",
          "hgvs_p": "p.Leu452Ile"
        }
      ],
      "clinvar_disease": "Immunodeficiency 23,Inborn genetic diseases,not provided",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "US:7 O:1",
      "phenotype_combined": "not provided|Immunodeficiency 23|Inborn genetic diseases",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}