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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: 16-14580878-TA-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=16&pos=14580878&ref=TA&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "16",
      "pos": 14580878,
      "ref": "TA",
      "alt": "T",
      "effect": "frameshift_variant",
      "transcript": "NM_002582.4",
      "consequences": [
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1257delT",
          "hgvs_p": "p.Phe419fs",
          "transcript": "NM_002582.4",
          "protein_id": "NP_002573.1",
          "transcript_support_level": null,
          "aa_start": 419,
          "aa_end": null,
          "aa_length": 639,
          "cds_start": 1257,
          "cds_end": null,
          "cds_length": 1920,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000437198.7",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_002582.4"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1257delT",
          "hgvs_p": "p.Phe419fs",
          "transcript": "ENST00000437198.7",
          "protein_id": "ENSP00000387911.2",
          "transcript_support_level": 1,
          "aa_start": 419,
          "aa_end": null,
          "aa_length": 639,
          "cds_start": 1257,
          "cds_end": null,
          "cds_length": 1920,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_002582.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000437198.7"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1257delT",
          "hgvs_p": "p.Phe419fs",
          "transcript": "ENST00000931608.1",
          "protein_id": "ENSP00000601667.1",
          "transcript_support_level": null,
          "aa_start": 419,
          "aa_end": null,
          "aa_length": 691,
          "cds_start": 1257,
          "cds_end": null,
          "cds_length": 2076,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000931608.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 25,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1332delT",
          "hgvs_p": "p.Phe444fs",
          "transcript": "ENST00000650990.1",
          "protein_id": "ENSP00000498741.1",
          "transcript_support_level": null,
          "aa_start": 444,
          "aa_end": null,
          "aa_length": 664,
          "cds_start": 1332,
          "cds_end": null,
          "cds_length": 1995,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000650990.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1257delT",
          "hgvs_p": "p.Phe419fs",
          "transcript": "ENST00000697474.1",
          "protein_id": "ENSP00000513329.1",
          "transcript_support_level": null,
          "aa_start": 419,
          "aa_end": null,
          "aa_length": 659,
          "cds_start": 1257,
          "cds_end": null,
          "cds_length": 1980,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000697474.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1254delT",
          "hgvs_p": "p.Phe418fs",
          "transcript": "ENST00000874419.1",
          "protein_id": "ENSP00000544478.1",
          "transcript_support_level": null,
          "aa_start": 418,
          "aa_end": null,
          "aa_length": 638,
          "cds_start": 1254,
          "cds_end": null,
          "cds_length": 1917,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000874419.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1332delT",
          "hgvs_p": "p.Phe444fs",
          "transcript": "ENST00000874418.1",
          "protein_id": "ENSP00000544477.1",
          "transcript_support_level": null,
          "aa_start": 444,
          "aa_end": null,
          "aa_length": 635,
          "cds_start": 1332,
          "cds_end": null,
          "cds_length": 1908,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000874418.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1236delT",
          "hgvs_p": "p.Phe412fs",
          "transcript": "ENST00000960024.1",
          "protein_id": "ENSP00000630083.1",
          "transcript_support_level": null,
          "aa_start": 412,
          "aa_end": null,
          "aa_length": 632,
          "cds_start": 1236,
          "cds_end": null,
          "cds_length": 1899,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000960024.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1206delT",
          "hgvs_p": "p.Phe402fs",
          "transcript": "ENST00000874417.1",
          "protein_id": "ENSP00000544476.1",
          "transcript_support_level": null,
          "aa_start": 402,
          "aa_end": null,
          "aa_length": 622,
          "cds_start": 1206,
          "cds_end": null,
          "cds_length": 1869,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000874417.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1200delT",
          "hgvs_p": "p.Phe400fs",
          "transcript": "ENST00000874421.1",
          "protein_id": "ENSP00000544480.1",
          "transcript_support_level": null,
          "aa_start": 400,
          "aa_end": null,
          "aa_length": 620,
          "cds_start": 1200,
          "cds_end": null,
          "cds_length": 1863,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000874421.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1191delT",
          "hgvs_p": "p.Phe397fs",
          "transcript": "ENST00000960023.1",
          "protein_id": "ENSP00000630082.1",
          "transcript_support_level": null,
          "aa_start": 397,
          "aa_end": null,
          "aa_length": 617,
          "cds_start": 1191,
          "cds_end": null,
          "cds_length": 1854,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000960023.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1182delT",
          "hgvs_p": "p.Phe394fs",
          "transcript": "ENST00000651865.1",
          "protein_id": "ENSP00000498567.1",
          "transcript_support_level": null,
          "aa_start": 394,
          "aa_end": null,
          "aa_length": 614,
          "cds_start": 1182,
          "cds_end": null,
          "cds_length": 1845,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000651865.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1179delT",
          "hgvs_p": "p.Phe393fs",
          "transcript": "ENST00000874415.1",
          "protein_id": "ENSP00000544474.1",
          "transcript_support_level": null,
          "aa_start": 393,
          "aa_end": null,
          "aa_length": 613,
          "cds_start": 1179,
          "cds_end": null,
          "cds_length": 1842,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000874415.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1176delT",
          "hgvs_p": "p.Phe392fs",
          "transcript": "ENST00000874420.1",
          "protein_id": "ENSP00000544479.1",
          "transcript_support_level": null,
          "aa_start": 392,
          "aa_end": null,
          "aa_length": 612,
          "cds_start": 1176,
          "cds_end": null,
          "cds_length": 1839,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000874420.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 16,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1170delT",
          "hgvs_p": "p.Phe390fs",
          "transcript": "ENST00000874414.1",
          "protein_id": "ENSP00000544473.1",
          "transcript_support_level": null,
          "aa_start": 390,
          "aa_end": null,
          "aa_length": 610,
          "cds_start": 1170,
          "cds_end": null,
          "cds_length": 1833,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000874414.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1257delT",
          "hgvs_p": "p.Phe419fs",
          "transcript": "ENST00000874416.1",
          "protein_id": "ENSP00000544475.1",
          "transcript_support_level": null,
          "aa_start": 419,
          "aa_end": null,
          "aa_length": 610,
          "cds_start": 1257,
          "cds_end": null,
          "cds_length": 1833,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000874416.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1170delT",
          "hgvs_p": "p.Phe390fs",
          "transcript": "ENST00000931610.1",
          "protein_id": "ENSP00000601669.1",
          "transcript_support_level": null,
          "aa_start": 390,
          "aa_end": null,
          "aa_length": 610,
          "cds_start": 1170,
          "cds_end": null,
          "cds_length": 1833,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000931610.1"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1119delT",
          "hgvs_p": "p.Phe373fs",
          "transcript": "NM_001242992.2",
          "protein_id": "NP_001229921.1",
          "transcript_support_level": null,
          "aa_start": 373,
          "aa_end": null,
          "aa_length": 593,
          "cds_start": 1119,
          "cds_end": null,
          "cds_length": 1782,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001242992.2"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 17,
          "exon_rank_end": null,
          "exon_count": 23,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1119delT",
          "hgvs_p": "p.Phe373fs",
          "transcript": "ENST00000420015.6",
          "protein_id": "ENSP00000410525.2",
          "transcript_support_level": 2,
          "aa_start": 373,
          "aa_end": null,
          "aa_length": 593,
          "cds_start": 1119,
          "cds_end": null,
          "cds_length": 1782,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000420015.6"
        },
        {
          "aa_ref": "F",
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 24,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PARN",
          "gene_hgnc_id": 8609,
          "hgvs_c": "c.1257delT",
          "hgvs_p": "p.Phe419fs",
          "transcript": "ENST00000650960.1",
          "protein_id": "ENSP00000499110.1",
          "transcript_support_level": null,
          "aa_start": 419,
          "aa_end": null,
          "aa_length": 590,
          "cds_start": 1257,
          "cds_end": null,
          "cds_length": 1773,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000650960.1"
        },
        {
          "aa_ref": "F",
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      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": null,
      "computational_prediction_selected": null,
      "computational_source_selected": null,
      "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": null,
      "bayesdelnoaf_prediction": null,
      "phylop100way_score": 5.288,
      "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": 10,
      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1,PP5_Moderate",
      "acmg_by_gene": [
        {
          "score": 10,
          "benign_score": 0,
          "pathogenic_score": 10,
          "criteria": [
            "PVS1",
            "PP5_Moderate"
          ],
          "verdict": "Pathogenic",
          "transcript": "NM_002582.4",
          "gene_symbol": "PARN",
          "hgnc_id": 8609,
          "effects": [
            "frameshift_variant"
          ],
          "inheritance_mode": "AD,AR,SD",
          "hgvs_c": "c.1257delT",
          "hgvs_p": "p.Phe419fs"
        }
      ],
      "clinvar_disease": " 4, Telomere-related, autosomal recessive 6,Dyskeratosis congenita,Familial Interstitial Pneumonia,Pulmonary fibrosis,Pulmonary fibrosis and/or bone marrow failure",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "P:1",
      "phenotype_combined": "Dyskeratosis congenita, autosomal recessive 6;Pulmonary fibrosis and/or bone marrow failure, Telomere-related, 4|Pulmonary fibrosis;Familial Interstitial Pneumonia",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}
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