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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: 6-75089146-A-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=6&pos=75089146&ref=A&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "6",
      "pos": 75089146,
      "ref": "A",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "ENST00000322507.13",
      "consequences": [
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 64,
          "exon_rank_end": null,
          "exon_count": 66,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL12A1",
          "gene_hgnc_id": 2188,
          "hgvs_c": "c.8970T>A",
          "hgvs_p": "p.Gly2990Gly",
          "transcript": "NM_004370.6",
          "protein_id": "NP_004361.3",
          "transcript_support_level": null,
          "aa_start": 2990,
          "aa_end": null,
          "aa_length": 3063,
          "cds_start": 8970,
          "cds_end": null,
          "cds_length": 9192,
          "cdna_start": 9282,
          "cdna_end": null,
          "cdna_length": 11725,
          "mane_select": "ENST00000322507.13",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 64,
          "exon_rank_end": null,
          "exon_count": 66,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL12A1",
          "gene_hgnc_id": 2188,
          "hgvs_c": "c.8970T>A",
          "hgvs_p": "p.Gly2990Gly",
          "transcript": "ENST00000322507.13",
          "protein_id": "ENSP00000325146.8",
          "transcript_support_level": 1,
          "aa_start": 2990,
          "aa_end": null,
          "aa_length": 3063,
          "cds_start": 8970,
          "cds_end": null,
          "cds_length": 9192,
          "cdna_start": 9282,
          "cdna_end": null,
          "cdna_length": 11725,
          "mane_select": "NM_004370.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 49,
          "exon_rank_end": null,
          "exon_count": 51,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL12A1",
          "gene_hgnc_id": 2188,
          "hgvs_c": "c.5478T>A",
          "hgvs_p": "p.Gly1826Gly",
          "transcript": "ENST00000345356.10",
          "protein_id": "ENSP00000305147.9",
          "transcript_support_level": 1,
          "aa_start": 1826,
          "aa_end": null,
          "aa_length": 1899,
          "cds_start": 5478,
          "cds_end": null,
          "cds_length": 5700,
          "cdna_start": 5588,
          "cdna_end": null,
          "cdna_length": 5886,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 64,
          "exon_rank_end": null,
          "exon_count": 66,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL12A1",
          "gene_hgnc_id": 2188,
          "hgvs_c": "c.8970T>A",
          "hgvs_p": "p.Gly2990Gly",
          "transcript": "NM_001424113.1",
          "protein_id": "NP_001411042.1",
          "transcript_support_level": null,
          "aa_start": 2990,
          "aa_end": null,
          "aa_length": 3118,
          "cds_start": 8970,
          "cds_end": null,
          "cds_length": 9357,
          "cdna_start": 9282,
          "cdna_end": null,
          "cdna_length": 10533,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 64,
          "exon_rank_end": null,
          "exon_count": 65,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL12A1",
          "gene_hgnc_id": 2188,
          "hgvs_c": "c.8958T>A",
          "hgvs_p": "p.Gly2986Gly",
          "transcript": "ENST00000483888.6",
          "protein_id": "ENSP00000421216.1",
          "transcript_support_level": 5,
          "aa_start": 2986,
          "aa_end": null,
          "aa_length": 3062,
          "cds_start": 8958,
          "cds_end": null,
          "cds_length": 9189,
          "cdna_start": 9039,
          "cdna_end": null,
          "cdna_length": 9637,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 63,
          "exon_rank_end": null,
          "exon_count": 65,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL12A1",
          "gene_hgnc_id": 2188,
          "hgvs_c": "c.8949T>A",
          "hgvs_p": "p.Gly2983Gly",
          "transcript": "NM_001424114.1",
          "protein_id": "NP_001411043.1",
          "transcript_support_level": null,
          "aa_start": 2983,
          "aa_end": null,
          "aa_length": 3056,
          "cds_start": 8949,
          "cds_end": null,
          "cds_length": 9171,
          "cdna_start": 9261,
          "cdna_end": null,
          "cdna_length": 11704,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 61,
          "exon_rank_end": null,
          "exon_count": 63,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL12A1",
          "gene_hgnc_id": 2188,
          "hgvs_c": "c.8742T>A",
          "hgvs_p": "p.Gly2914Gly",
          "transcript": "ENST00000416123.6",
          "protein_id": "ENSP00000412864.2",
          "transcript_support_level": 5,
          "aa_start": 2914,
          "aa_end": null,
          "aa_length": 2987,
          "cds_start": 8742,
          "cds_end": null,
          "cds_length": 8964,
          "cdna_start": 8742,
          "cdna_end": null,
          "cdna_length": 8964,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 63,
          "exon_rank_end": null,
          "exon_count": 65,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL12A1",
          "gene_hgnc_id": 2188,
          "hgvs_c": "c.8697T>A",
          "hgvs_p": "p.Gly2899Gly",
          "transcript": "NM_001424115.1",
          "protein_id": "NP_001411044.1",
          "transcript_support_level": null,
          "aa_start": 2899,
          "aa_end": null,
          "aa_length": 2972,
          "cds_start": 8697,
          "cds_end": null,
          "cds_length": 8919,
          "cdna_start": 9009,
          "cdna_end": null,
          "cdna_length": 11452,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 49,
          "exon_rank_end": null,
          "exon_count": 51,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL12A1",
          "gene_hgnc_id": 2188,
          "hgvs_c": "c.5478T>A",
          "hgvs_p": "p.Gly1826Gly",
          "transcript": "NM_001424116.1",
          "protein_id": "NP_001411045.1",
          "transcript_support_level": null,
          "aa_start": 1826,
          "aa_end": null,
          "aa_length": 1954,
          "cds_start": 5478,
          "cds_end": null,
          "cds_length": 5865,
          "cdna_start": 5790,
          "cdna_end": null,
          "cdna_length": 7041,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 49,
          "exon_rank_end": null,
          "exon_count": 51,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL12A1",
          "gene_hgnc_id": 2188,
          "hgvs_c": "c.5478T>A",
          "hgvs_p": "p.Gly1826Gly",
          "transcript": "NM_080645.3",
          "protein_id": "NP_542376.2",
          "transcript_support_level": null,
          "aa_start": 1826,
          "aa_end": null,
          "aa_length": 1899,
          "cds_start": 5478,
          "cds_end": null,
          "cds_length": 5700,
          "cdna_start": 5790,
          "cdna_end": null,
          "cdna_length": 8233,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL12A1",
          "gene_hgnc_id": 2188,
          "hgvs_c": "c.1884T>A",
          "hgvs_p": "p.Gly628Gly",
          "transcript": "ENST00000425443.6",
          "protein_id": "ENSP00000399812.2",
          "transcript_support_level": 5,
          "aa_start": 628,
          "aa_end": null,
          "aa_length": 756,
          "cds_start": 1884,
          "cds_end": null,
          "cds_length": 2271,
          "cdna_start": 1884,
          "cdna_end": null,
          "cdna_length": 3135,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 64,
          "exon_rank_end": null,
          "exon_count": 66,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL12A1",
          "gene_hgnc_id": 2188,
          "hgvs_c": "c.8970T>A",
          "hgvs_p": "p.Gly2990Gly",
          "transcript": "XM_047418184.1",
          "protein_id": "XP_047274140.1",
          "transcript_support_level": null,
          "aa_start": 2990,
          "aa_end": null,
          "aa_length": 3118,
          "cds_start": 8970,
          "cds_end": null,
          "cds_length": 9357,
          "cdna_start": 9332,
          "cdna_end": null,
          "cdna_length": 10583,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 63,
          "exon_rank_end": null,
          "exon_count": 65,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL12A1",
          "gene_hgnc_id": 2188,
          "hgvs_c": "c.8934T>A",
          "hgvs_p": "p.Gly2978Gly",
          "transcript": "XM_017010252.3",
          "protein_id": "XP_016865741.1",
          "transcript_support_level": null,
          "aa_start": 2978,
          "aa_end": null,
          "aa_length": 3106,
          "cds_start": 8934,
          "cds_end": null,
          "cds_length": 9321,
          "cdna_start": 9529,
          "cdna_end": null,
          "cdna_length": 10780,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 63,
          "exon_rank_end": null,
          "exon_count": 65,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL12A1",
          "gene_hgnc_id": 2188,
          "hgvs_c": "c.8697T>A",
          "hgvs_p": "p.Gly2899Gly",
          "transcript": "XM_011535435.2",
          "protein_id": "XP_011533737.1",
          "transcript_support_level": null,
          "aa_start": 2899,
          "aa_end": null,
          "aa_length": 3027,
          "cds_start": 8697,
          "cds_end": null,
          "cds_length": 9084,
          "cdna_start": 9009,
          "cdna_end": null,
          "cdna_length": 10260,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "G",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 49,
          "exon_rank_end": null,
          "exon_count": 51,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL12A1",
          "gene_hgnc_id": 2188,
          "hgvs_c": "c.5478T>A",
          "hgvs_p": "p.Gly1826Gly",
          "transcript": "XM_047418186.1",
          "protein_id": "XP_047274142.1",
          "transcript_support_level": null,
          "aa_start": 1826,
          "aa_end": null,
          "aa_length": 1899,
          "cds_start": 5478,
          "cds_end": null,
          "cds_length": 5700,
          "cdna_start": 5840,
          "cdna_end": null,
          "cdna_length": 8283,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 2,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL12A1",
          "gene_hgnc_id": 2188,
          "hgvs_c": "n.379T>A",
          "hgvs_p": null,
          "transcript": "ENST00000680981.1",
          "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": 2782,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "downstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "COL12A1",
          "gene_hgnc_id": 2188,
          "hgvs_c": "n.*14T>A",
          "hgvs_p": null,
          "transcript": "ENST00000511023.1",
          "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": 571,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "COL12A1",
      "gene_hgnc_id": 2188,
      "dbsnp": "rs190501064",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.800000011920929,
      "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": -0.8,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -1.095,
      "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": -3,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong,BP7",
      "acmg_by_gene": [
        {
          "score": -3,
          "benign_score": 5,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000322507.13",
          "gene_symbol": "COL12A1",
          "hgnc_id": 2188,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.8970T>A",
          "hgvs_p": "p.Gly2990Gly"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}