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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: 16-79599192-CCCGCCGCCTCCGCCG-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=79599192&ref=CCCGCCGCCTCCGCCG&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "16",
      "pos": 79599192,
      "ref": "CCCGCCGCCTCCGCCG",
      "alt": "C",
      "effect": "disruptive_inframe_deletion",
      "transcript": "ENST00000326043.5",
      "consequences": [
        {
          "aa_ref": "GGGGGG",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MAF",
          "gene_hgnc_id": 6776,
          "hgvs_c": "c.696_710delCGGCGGAGGCGGCGG",
          "hgvs_p": "p.Gly233_Gly237del",
          "transcript": "NM_005360.5",
          "protein_id": "NP_005351.2",
          "transcript_support_level": null,
          "aa_start": 232,
          "aa_end": null,
          "aa_length": 403,
          "cds_start": 696,
          "cds_end": null,
          "cds_length": 1212,
          "cdna_start": 1545,
          "cdna_end": null,
          "cdna_length": 2669,
          "mane_select": "ENST00000326043.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "GGGGGG",
          "aa_alt": "G",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MAF",
          "gene_hgnc_id": 6776,
          "hgvs_c": "c.696_710delCGGCGGAGGCGGCGG",
          "hgvs_p": "p.Gly233_Gly237del",
          "transcript": "ENST00000326043.5",
          "protein_id": "ENSP00000327048.4",
          "transcript_support_level": 1,
          "aa_start": 232,
          "aa_end": null,
          "aa_length": 403,
          "cds_start": 696,
          "cds_end": null,
          "cds_length": 1212,
          "cdna_start": 1545,
          "cdna_end": null,
          "cdna_length": 2669,
          "mane_select": "NM_005360.5",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "GGGGGG",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MAF",
          "gene_hgnc_id": 6776,
          "hgvs_c": "c.696_710delCGGCGGAGGCGGCGG",
          "hgvs_p": "p.Gly233_Gly237del",
          "transcript": "ENST00000569649.1",
          "protein_id": "ENSP00000455097.1",
          "transcript_support_level": 5,
          "aa_start": 232,
          "aa_end": null,
          "aa_length": 383,
          "cds_start": 696,
          "cds_end": null,
          "cds_length": 1152,
          "cdna_start": 710,
          "cdna_end": null,
          "cdna_length": 1217,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "GGGGGG",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 1,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MAF",
          "gene_hgnc_id": 6776,
          "hgvs_c": "c.696_710delCGGCGGAGGCGGCGG",
          "hgvs_p": "p.Gly233_Gly237del",
          "transcript": "NM_001031804.3",
          "protein_id": "NP_001026974.1",
          "transcript_support_level": null,
          "aa_start": 232,
          "aa_end": null,
          "aa_length": 373,
          "cds_start": 696,
          "cds_end": null,
          "cds_length": 1122,
          "cdna_start": 1545,
          "cdna_end": null,
          "cdna_length": 6900,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "GGGGGG",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 1,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MAF",
          "gene_hgnc_id": 6776,
          "hgvs_c": "c.696_710delCGGCGGAGGCGGCGG",
          "hgvs_p": "p.Gly233_Gly237del",
          "transcript": "ENST00000393350.1",
          "protein_id": "ENSP00000377019.1",
          "transcript_support_level": 6,
          "aa_start": 232,
          "aa_end": null,
          "aa_length": 373,
          "cds_start": 696,
          "cds_end": null,
          "cds_length": 1122,
          "cdna_start": 1522,
          "cdna_end": null,
          "cdna_length": 6384,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "GGGGGG",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MAF",
          "gene_hgnc_id": 6776,
          "hgvs_c": "c.696_710delCGGCGGAGGCGGCGG",
          "hgvs_p": "p.Gly233_Gly237del",
          "transcript": "XM_017023233.3",
          "protein_id": "XP_016878722.1",
          "transcript_support_level": null,
          "aa_start": 232,
          "aa_end": null,
          "aa_length": 383,
          "cds_start": 696,
          "cds_end": null,
          "cds_length": 1152,
          "cdna_start": 1545,
          "cdna_end": null,
          "cdna_length": 2250,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "GGGGGG",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MAF",
          "gene_hgnc_id": 6776,
          "hgvs_c": "c.696_710delCGGCGGAGGCGGCGG",
          "hgvs_p": "p.Gly233_Gly237del",
          "transcript": "XM_017023234.3",
          "protein_id": "XP_016878723.1",
          "transcript_support_level": null,
          "aa_start": 232,
          "aa_end": null,
          "aa_length": 383,
          "cds_start": 696,
          "cds_end": null,
          "cds_length": 1152,
          "cdna_start": 1545,
          "cdna_end": null,
          "cdna_length": 3317,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "GGGGGG",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MAF",
          "gene_hgnc_id": 6776,
          "hgvs_c": "c.696_710delCGGCGGAGGCGGCGG",
          "hgvs_p": "p.Gly233_Gly237del",
          "transcript": "XM_017023235.3",
          "protein_id": "XP_016878724.1",
          "transcript_support_level": null,
          "aa_start": 232,
          "aa_end": null,
          "aa_length": 383,
          "cds_start": 696,
          "cds_end": null,
          "cds_length": 1152,
          "cdna_start": 1545,
          "cdna_end": null,
          "cdna_length": 4675,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "GGGGGG",
          "aa_alt": "G",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MAF",
          "gene_hgnc_id": 6776,
          "hgvs_c": "c.696_710delCGGCGGAGGCGGCGG",
          "hgvs_p": "p.Gly233_Gly237del",
          "transcript": "XM_024450279.2",
          "protein_id": "XP_024306047.1",
          "transcript_support_level": null,
          "aa_start": 232,
          "aa_end": null,
          "aa_length": 383,
          "cds_start": 696,
          "cds_end": null,
          "cds_length": 1152,
          "cdna_start": 1545,
          "cdna_end": null,
          "cdna_length": 12295,
          "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": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MAF",
          "gene_hgnc_id": 6776,
          "hgvs_c": "n.1531_1545delCGGCGGAGGCGGCGG",
          "hgvs_p": null,
          "transcript": "XR_001751902.3",
          "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": 10744,
          "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": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MAF",
          "gene_hgnc_id": 6776,
          "hgvs_c": "n.1531_1545delCGGCGGAGGCGGCGG",
          "hgvs_p": null,
          "transcript": "XR_002957802.2",
          "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": 11361,
          "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": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MAF",
          "gene_hgnc_id": 6776,
          "hgvs_c": "n.1531_1545delCGGCGGAGGCGGCGG",
          "hgvs_p": null,
          "transcript": "XR_002957803.2",
          "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": 11747,
          "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": 4,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "MAF",
          "gene_hgnc_id": 6776,
          "hgvs_c": "n.1531_1545delCGGCGGAGGCGGCGG",
          "hgvs_p": null,
          "transcript": "XR_002957804.2",
          "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": 10672,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "MAF",
      "gene_hgnc_id": 6776,
      "dbsnp": "rs1229626204",
      "frequency_reference_population": 0.0003175432,
      "hom_count_reference_population": 1,
      "allele_count_reference_population": 326,
      "gnomad_exomes_af": 0.000107844,
      "gnomad_genomes_af": 0.00158517,
      "gnomad_exomes_ac": 95,
      "gnomad_genomes_ac": 231,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": 1,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": null,
      "computational_prediction_selected": null,
      "computational_source_selected": null,
      "splice_score_selected": null,
      "splice_prediction_selected": null,
      "splice_source_selected": null,
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": null,
      "bayesdelnoaf_prediction": null,
      "phylop100way_score": 1.646,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": null,
      "spliceai_max_prediction": null,
      "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": "BP3,BP6_Very_Strong",
      "acmg_by_gene": [
        {
          "score": -9,
          "benign_score": 9,
          "pathogenic_score": 0,
          "criteria": [
            "BP3",
            "BP6_Very_Strong"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000326043.5",
          "gene_symbol": "MAF",
          "hgnc_id": 6776,
          "effects": [
            "disruptive_inframe_deletion"
          ],
          "inheritance_mode": "AD,AR",
          "hgvs_c": "c.696_710delCGGCGGAGGCGGCGG",
          "hgvs_p": "p.Gly233_Gly237del"
        }
      ],
      "clinvar_disease": "Ayme-Gripp syndrome,Cataract 21 multiple types,Inborn genetic diseases,not provided",
      "clinvar_classification": "Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:3",
      "phenotype_combined": "Cataract 21 multiple types;Ayme-Gripp syndrome|Inborn genetic diseases|not provided",
      "pathogenicity_classification_combined": "Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}