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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: 19-10133690-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=10133690&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "19",
      "pos": 10133690,
      "ref": "C",
      "alt": "T",
      "effect": "missense_variant",
      "transcript": "NM_001130823.3",
      "consequences": [
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 41,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "c.4876G>A",
          "hgvs_p": "p.Glu1626Lys",
          "transcript": "NM_001130823.3",
          "protein_id": "NP_001124295.1",
          "transcript_support_level": null,
          "aa_start": 1626,
          "aa_end": null,
          "aa_length": 1632,
          "cds_start": 4876,
          "cds_end": null,
          "cds_length": 4899,
          "cdna_start": 4930,
          "cdna_end": null,
          "cdna_length": 5274,
          "mane_select": "ENST00000359526.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 41,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "c.4876G>A",
          "hgvs_p": "p.Glu1626Lys",
          "transcript": "ENST00000359526.9",
          "protein_id": "ENSP00000352516.3",
          "transcript_support_level": 1,
          "aa_start": 1626,
          "aa_end": null,
          "aa_length": 1632,
          "cds_start": 4876,
          "cds_end": null,
          "cds_length": 4899,
          "cdna_start": 4930,
          "cdna_end": null,
          "cdna_length": 5274,
          "mane_select": "NM_001130823.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 40,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "c.4828G>A",
          "hgvs_p": "p.Glu1610Lys",
          "transcript": "ENST00000340748.8",
          "protein_id": "ENSP00000345739.3",
          "transcript_support_level": 1,
          "aa_start": 1610,
          "aa_end": null,
          "aa_length": 1616,
          "cds_start": 4828,
          "cds_end": null,
          "cds_length": 4851,
          "cdna_start": 5064,
          "cdna_end": null,
          "cdna_length": 5408,
          "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": 41,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "n.*4566G>A",
          "hgvs_p": null,
          "transcript": "ENST00000592705.5",
          "protein_id": "ENSP00000466657.1",
          "transcript_support_level": 1,
          "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": 5215,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 41,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "n.*4566G>A",
          "hgvs_p": null,
          "transcript": "ENST00000592705.5",
          "protein_id": "ENSP00000466657.1",
          "transcript_support_level": 1,
          "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": 5215,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 40,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "c.4837G>A",
          "hgvs_p": "p.Glu1613Lys",
          "transcript": "NM_001318730.2",
          "protein_id": "NP_001305659.1",
          "transcript_support_level": null,
          "aa_start": 1613,
          "aa_end": null,
          "aa_length": 1619,
          "cds_start": 4837,
          "cds_end": null,
          "cds_length": 4860,
          "cdna_start": 4891,
          "cdna_end": null,
          "cdna_length": 5235,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 40,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "c.4828G>A",
          "hgvs_p": "p.Glu1610Lys",
          "transcript": "NM_001379.4",
          "protein_id": "NP_001370.1",
          "transcript_support_level": null,
          "aa_start": 1610,
          "aa_end": null,
          "aa_length": 1616,
          "cds_start": 4828,
          "cds_end": null,
          "cds_length": 4851,
          "cdna_start": 4882,
          "cdna_end": null,
          "cdna_length": 5226,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "E",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "missense_variant"
          ],
          "exon_rank": 41,
          "exon_rank_end": null,
          "exon_count": 41,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "c.4513G>A",
          "hgvs_p": "p.Glu1505Lys",
          "transcript": "NM_001318731.2",
          "protein_id": "NP_001305660.1",
          "transcript_support_level": null,
          "aa_start": 1505,
          "aa_end": null,
          "aa_length": 1511,
          "cds_start": 4513,
          "cds_end": null,
          "cds_length": 4536,
          "cdna_start": 4890,
          "cdna_end": null,
          "cdna_length": 5234,
          "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": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "n.2749G>A",
          "hgvs_p": null,
          "transcript": "ENST00000586588.5",
          "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": 3094,
          "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": 18,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "n.2911G>A",
          "hgvs_p": null,
          "transcript": "ENST00000586667.2",
          "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": 3259,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "n.*283G>A",
          "hgvs_p": null,
          "transcript": "ENST00000588913.5",
          "protein_id": "ENSP00000467125.1",
          "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": 1775,
          "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": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "n.4062G>A",
          "hgvs_p": null,
          "transcript": "ENST00000589351.6",
          "protein_id": null,
          "transcript_support_level": 2,
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          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 4395,
          "mane_select": null,
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        },
        {
          "aa_ref": null,
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          "canonical": false,
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          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "n.182G>A",
          "hgvs_p": null,
          "transcript": "ENST00000591798.5",
          "protein_id": null,
          "transcript_support_level": 3,
          "aa_start": null,
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          "cdna_start": null,
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          "cdna_length": 521,
          "mane_select": null,
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          "biotype": null,
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        },
        {
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          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 37,
          "exon_rank_end": null,
          "exon_count": 37,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "n.4488G>A",
          "hgvs_p": null,
          "transcript": "ENST00000676604.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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          "cdna_start": null,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
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          "gene_symbol": "DNMT1",
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          "hgvs_c": "n.5722G>A",
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        },
        {
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          "canonical": false,
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          "consequences": [
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          ],
          "exon_rank": 30,
          "exon_rank_end": null,
          "exon_count": 30,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "n.5512G>A",
          "hgvs_p": null,
          "transcript": "ENST00000676868.1",
          "protein_id": null,
          "transcript_support_level": null,
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          "cdna_length": 5845,
          "mane_select": null,
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          "feature": null
        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 40,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "n.*4518G>A",
          "hgvs_p": null,
          "transcript": "ENST00000677013.1",
          "protein_id": "ENSP00000503135.1",
          "transcript_support_level": null,
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          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "n.1424G>A",
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        },
        {
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          ],
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          "exon_rank_end": null,
          "exon_count": 2,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "n.357G>A",
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          "transcript": "ENST00000677135.1",
          "protein_id": null,
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        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 39,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "n.*3948G>A",
          "hgvs_p": null,
          "transcript": "ENST00000677250.1",
          "protein_id": "ENSP00000502894.1",
          "transcript_support_level": null,
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          "aa_length": null,
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          "cdna_start": null,
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          "cdna_length": 5127,
          "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": 39,
          "exon_rank_end": null,
          "exon_count": 39,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "DNMT1",
          "gene_hgnc_id": 2976,
          "hgvs_c": "n.*1098G>A",
          "hgvs_p": null,
          "transcript": "ENST00000677616.1",
          "protein_id": "ENSP00000503055.1",
          "transcript_support_level": null,
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      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": 0.005883991718292236,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "MetaRNN",
      "splice_score_selected": 0.009999999776482582,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": 0.032,
      "revel_prediction": "Benign",
      "alphamissense_score": 0.0785,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.54,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.139,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0.01,
      "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,BP6,BS2",
      "acmg_by_gene": [
        {
          "score": -9,
          "benign_score": 9,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "NM_001130823.3",
          "gene_symbol": "DNMT1",
          "hgnc_id": 2976,
          "effects": [
            "missense_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "c.4876G>A",
          "hgvs_p": "p.Glu1626Lys"
        }
      ],
      "clinvar_disease": "Hereditary sensory neuropathy-deafness-dementia syndrome,Inborn genetic diseases,not provided",
      "clinvar_classification": "Conflicting classifications of pathogenicity",
      "clinvar_review_status": "criteria provided, conflicting classifications",
      "clinvar_submissions_summary": "US:1 LB:3 B:1",
      "phenotype_combined": "not provided|Hereditary sensory neuropathy-deafness-dementia syndrome|Inborn genetic diseases",
      "pathogenicity_classification_combined": "Conflicting classifications of pathogenicity",
      "custom_annotations": null
    }
  ],
  "message": null
}