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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: 14-75018865-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=75018865&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "14",
      "pos": 75018865,
      "ref": "C",
      "alt": "A",
      "effect": "synonymous_variant",
      "transcript": "NM_001040108.2",
      "consequences": [
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "c.4206G>T",
          "hgvs_p": "p.Pro1402Pro",
          "transcript": "NM_001040108.2",
          "protein_id": "NP_001035197.1",
          "transcript_support_level": null,
          "aa_start": 1402,
          "aa_end": null,
          "aa_length": 1453,
          "cds_start": 4206,
          "cds_end": null,
          "cds_length": 4362,
          "cdna_start": 4357,
          "cdna_end": null,
          "cdna_length": 7820,
          "mane_select": "ENST00000355774.7",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "c.4206G>T",
          "hgvs_p": "p.Pro1402Pro",
          "transcript": "ENST00000355774.7",
          "protein_id": "ENSP00000348020.2",
          "transcript_support_level": 5,
          "aa_start": 1402,
          "aa_end": null,
          "aa_length": 1453,
          "cds_start": 4206,
          "cds_end": null,
          "cds_length": 4362,
          "cdna_start": 4357,
          "cdna_end": null,
          "cdna_length": 7820,
          "mane_select": "NM_001040108.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "c.4134G>T",
          "hgvs_p": "p.Pro1378Pro",
          "transcript": "ENST00000380968.6",
          "protein_id": "ENSP00000370355.3",
          "transcript_support_level": 1,
          "aa_start": 1378,
          "aa_end": null,
          "aa_length": 1429,
          "cds_start": 4134,
          "cds_end": null,
          "cds_length": 4290,
          "cdna_start": 4350,
          "cdna_end": null,
          "cdna_length": 7819,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "c.4134G>T",
          "hgvs_p": "p.Pro1378Pro",
          "transcript": "NM_014381.3",
          "protein_id": "NP_055196.2",
          "transcript_support_level": null,
          "aa_start": 1378,
          "aa_end": null,
          "aa_length": 1429,
          "cds_start": 4134,
          "cds_end": null,
          "cds_length": 4290,
          "cdna_start": 4285,
          "cdna_end": null,
          "cdna_length": 7748,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 6,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "c.3672G>T",
          "hgvs_p": "p.Pro1224Pro",
          "transcript": "ENST00000556257.5",
          "protein_id": "ENSP00000451540.1",
          "transcript_support_level": 5,
          "aa_start": 1224,
          "aa_end": null,
          "aa_length": 1275,
          "cds_start": 3672,
          "cds_end": null,
          "cds_length": 3828,
          "cdna_start": 3778,
          "cdna_end": null,
          "cdna_length": 4229,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "c.1275G>T",
          "hgvs_p": "p.Pro425Pro",
          "transcript": "ENST00000553713.5",
          "protein_id": "ENSP00000451130.1",
          "transcript_support_level": 5,
          "aa_start": 425,
          "aa_end": null,
          "aa_length": 476,
          "cds_start": 1275,
          "cds_end": null,
          "cds_length": 1431,
          "cdna_start": 1277,
          "cdna_end": null,
          "cdna_length": 2118,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "c.4206G>T",
          "hgvs_p": "p.Pro1402Pro",
          "transcript": "XM_006720116.5",
          "protein_id": "XP_006720179.1",
          "transcript_support_level": null,
          "aa_start": 1402,
          "aa_end": null,
          "aa_length": 1453,
          "cds_start": 4206,
          "cds_end": null,
          "cds_length": 4362,
          "cdna_start": 4298,
          "cdna_end": null,
          "cdna_length": 7761,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "c.4134G>T",
          "hgvs_p": "p.Pro1378Pro",
          "transcript": "XM_017021219.3",
          "protein_id": "XP_016876708.1",
          "transcript_support_level": null,
          "aa_start": 1378,
          "aa_end": null,
          "aa_length": 1429,
          "cds_start": 4134,
          "cds_end": null,
          "cds_length": 4290,
          "cdna_start": 4226,
          "cdna_end": null,
          "cdna_length": 7689,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "c.4101G>T",
          "hgvs_p": "p.Pro1367Pro",
          "transcript": "XM_005267532.6",
          "protein_id": "XP_005267589.1",
          "transcript_support_level": null,
          "aa_start": 1367,
          "aa_end": null,
          "aa_length": 1418,
          "cds_start": 4101,
          "cds_end": null,
          "cds_length": 4257,
          "cdna_start": 4252,
          "cdna_end": null,
          "cdna_length": 7715,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 11,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "c.4101G>T",
          "hgvs_p": "p.Pro1367Pro",
          "transcript": "XM_024449538.2",
          "protein_id": "XP_024305306.1",
          "transcript_support_level": null,
          "aa_start": 1367,
          "aa_end": null,
          "aa_length": 1418,
          "cds_start": 4101,
          "cds_end": null,
          "cds_length": 4257,
          "cdna_start": 4193,
          "cdna_end": null,
          "cdna_length": 7656,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "c.4029G>T",
          "hgvs_p": "p.Pro1343Pro",
          "transcript": "XM_005267533.6",
          "protein_id": "XP_005267590.1",
          "transcript_support_level": null,
          "aa_start": 1343,
          "aa_end": null,
          "aa_length": 1394,
          "cds_start": 4029,
          "cds_end": null,
          "cds_length": 4185,
          "cdna_start": 4180,
          "cdna_end": null,
          "cdna_length": 7643,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 10,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "c.4029G>T",
          "hgvs_p": "p.Pro1343Pro",
          "transcript": "XM_047431265.1",
          "protein_id": "XP_047287221.1",
          "transcript_support_level": null,
          "aa_start": 1343,
          "aa_end": null,
          "aa_length": 1394,
          "cds_start": 4029,
          "cds_end": null,
          "cds_length": 4185,
          "cdna_start": 4121,
          "cdna_end": null,
          "cdna_length": 7584,
          "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": 3,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "n.219G>T",
          "hgvs_p": null,
          "transcript": "ENST00000554697.5",
          "protein_id": "ENSP00000451055.1",
          "transcript_support_level": 3,
          "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": 825,
          "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": 1,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "n.248G>T",
          "hgvs_p": null,
          "transcript": "ENST00000555415.1",
          "protein_id": null,
          "transcript_support_level": 2,
          "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": 700,
          "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": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "n.4285G>T",
          "hgvs_p": null,
          "transcript": "XR_001750225.3",
          "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": 6603,
          "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": 11,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "n.4252G>T",
          "hgvs_p": null,
          "transcript": "XR_007064004.1",
          "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": 6570,
          "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": 10,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "n.4180G>T",
          "hgvs_p": null,
          "transcript": "XR_007064005.1",
          "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": 6498,
          "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": 12,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "n.4357G>T",
          "hgvs_p": null,
          "transcript": "XR_245681.5",
          "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": 6675,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "downstream_gene_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MLH3",
          "gene_hgnc_id": 7128,
          "hgvs_c": "c.*152G>T",
          "hgvs_p": null,
          "transcript": "XM_047431266.1",
          "protein_id": "XP_047287222.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 1297,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 3894,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4118,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "MLH3",
      "gene_hgnc_id": 7128,
      "dbsnp": "rs772429784",
      "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": 0.04800000041723251,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "REVEL",
      "splice_score_selected": 0.029999999329447746,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.048,
      "revel_prediction": "Benign",
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.62,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": -5.207,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.03,
      "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_Moderate,BP6_Moderate,BP7",
      "acmg_by_gene": [
        {
          "score": -3,
          "benign_score": 5,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Moderate",
            "BP6_Moderate",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_001040108.2",
          "gene_symbol": "MLH3",
          "hgnc_id": 7128,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.4206G>T",
          "hgvs_p": "p.Pro1402Pro"
        }
      ],
      "clinvar_disease": "not specified",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "LB:1",
      "phenotype_combined": "not specified",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}