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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: 13-51934843-C-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=13&pos=51934843&ref=C&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "13",
      "pos": 51934843,
      "ref": "C",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "ENST00000242839.10",
      "consequences": [
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4311G>A",
          "hgvs_p": "p.Lys1437Lys",
          "transcript": "NM_000053.4",
          "protein_id": "NP_000044.2",
          "transcript_support_level": null,
          "aa_start": 1437,
          "aa_end": null,
          "aa_length": 1465,
          "cds_start": 4311,
          "cds_end": null,
          "cds_length": 4398,
          "cdna_start": 4424,
          "cdna_end": null,
          "cdna_length": 6598,
          "mane_select": "ENST00000242839.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4311G>A",
          "hgvs_p": "p.Lys1437Lys",
          "transcript": "ENST00000242839.10",
          "protein_id": "ENSP00000242839.5",
          "transcript_support_level": 1,
          "aa_start": 1437,
          "aa_end": null,
          "aa_length": 1465,
          "cds_start": 4311,
          "cds_end": null,
          "cds_length": 4398,
          "cdna_start": 4424,
          "cdna_end": null,
          "cdna_length": 6598,
          "mane_select": "NM_000053.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4167G>A",
          "hgvs_p": "p.Lys1389Lys",
          "transcript": "ENST00000634844.1",
          "protein_id": "ENSP00000489398.1",
          "transcript_support_level": 1,
          "aa_start": 1389,
          "aa_end": null,
          "aa_length": 1417,
          "cds_start": 4167,
          "cds_end": null,
          "cds_length": 4254,
          "cdna_start": 4241,
          "cdna_end": null,
          "cdna_length": 4398,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4116G>A",
          "hgvs_p": "p.Lys1372Lys",
          "transcript": "ENST00000418097.7",
          "protein_id": "ENSP00000393343.2",
          "transcript_support_level": 1,
          "aa_start": 1372,
          "aa_end": null,
          "aa_length": 1400,
          "cds_start": 4116,
          "cds_end": null,
          "cds_length": 4203,
          "cdna_start": 4190,
          "cdna_end": null,
          "cdna_length": 4340,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4059G>A",
          "hgvs_p": "p.Lys1353Lys",
          "transcript": "ENST00000448424.7",
          "protein_id": "ENSP00000416738.3",
          "transcript_support_level": 1,
          "aa_start": 1353,
          "aa_end": null,
          "aa_length": 1381,
          "cds_start": 4059,
          "cds_end": null,
          "cds_length": 4146,
          "cdna_start": 4312,
          "cdna_end": null,
          "cdna_length": 6451,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3978G>A",
          "hgvs_p": "p.Lys1326Lys",
          "transcript": "ENST00000400366.6",
          "protein_id": "ENSP00000383217.3",
          "transcript_support_level": 1,
          "aa_start": 1326,
          "aa_end": null,
          "aa_length": 1354,
          "cds_start": 3978,
          "cds_end": null,
          "cds_length": 4065,
          "cdna_start": 3978,
          "cdna_end": null,
          "cdna_length": 4065,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 13,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3021G>A",
          "hgvs_p": "p.Lys1007Lys",
          "transcript": "ENST00000400370.8",
          "protein_id": "ENSP00000383221.3",
          "transcript_support_level": 1,
          "aa_start": 1007,
          "aa_end": null,
          "aa_length": 1035,
          "cds_start": 3021,
          "cds_end": null,
          "cds_length": 3108,
          "cdna_start": 3095,
          "cdna_end": null,
          "cdna_length": 3252,
          "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": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.*1412G>A",
          "hgvs_p": null,
          "transcript": "ENST00000634308.1",
          "protein_id": "ENSP00000489234.1",
          "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": 4321,
          "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": 17,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.5055G>A",
          "hgvs_p": null,
          "transcript": "ENST00000634620.1",
          "protein_id": null,
          "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": 5653,
          "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": 14,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.3656G>A",
          "hgvs_p": null,
          "transcript": "ENST00000634810.1",
          "protein_id": null,
          "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": 5825,
          "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": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.*1412G>A",
          "hgvs_p": null,
          "transcript": "ENST00000634308.1",
          "protein_id": "ENSP00000489234.1",
          "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": 4321,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4311G>A",
          "hgvs_p": "p.Lys1437Lys",
          "transcript": "NM_001406511.1",
          "protein_id": "NP_001393440.1",
          "transcript_support_level": null,
          "aa_start": 1437,
          "aa_end": null,
          "aa_length": 1465,
          "cds_start": 4311,
          "cds_end": null,
          "cds_length": 4398,
          "cdna_start": 4478,
          "cdna_end": null,
          "cdna_length": 6652,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4311G>A",
          "hgvs_p": "p.Lys1437Lys",
          "transcript": "NM_001406512.1",
          "protein_id": "NP_001393441.1",
          "transcript_support_level": null,
          "aa_start": 1437,
          "aa_end": null,
          "aa_length": 1465,
          "cds_start": 4311,
          "cds_end": null,
          "cds_length": 4398,
          "cdna_start": 4717,
          "cdna_end": null,
          "cdna_length": 6891,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4305G>A",
          "hgvs_p": "p.Lys1435Lys",
          "transcript": "NM_001406513.1",
          "protein_id": "NP_001393442.1",
          "transcript_support_level": null,
          "aa_start": 1435,
          "aa_end": null,
          "aa_length": 1463,
          "cds_start": 4305,
          "cds_end": null,
          "cds_length": 4392,
          "cdna_start": 4472,
          "cdna_end": null,
          "cdna_length": 6646,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4278G>A",
          "hgvs_p": "p.Lys1426Lys",
          "transcript": "NM_001406514.1",
          "protein_id": "NP_001393443.1",
          "transcript_support_level": null,
          "aa_start": 1426,
          "aa_end": null,
          "aa_length": 1454,
          "cds_start": 4278,
          "cds_end": null,
          "cds_length": 4365,
          "cdna_start": 4391,
          "cdna_end": null,
          "cdna_length": 6565,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4257G>A",
          "hgvs_p": "p.Lys1419Lys",
          "transcript": "NM_001406515.1",
          "protein_id": "NP_001393444.1",
          "transcript_support_level": null,
          "aa_start": 1419,
          "aa_end": null,
          "aa_length": 1447,
          "cds_start": 4257,
          "cds_end": null,
          "cds_length": 4344,
          "cdna_start": 4370,
          "cdna_end": null,
          "cdna_length": 6544,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4257G>A",
          "hgvs_p": "p.Lys1419Lys",
          "transcript": "NM_001406516.1",
          "protein_id": "NP_001393445.1",
          "transcript_support_level": null,
          "aa_start": 1419,
          "aa_end": null,
          "aa_length": 1447,
          "cds_start": 4257,
          "cds_end": null,
          "cds_length": 4344,
          "cdna_start": 4663,
          "cdna_end": null,
          "cdna_length": 6837,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4215G>A",
          "hgvs_p": "p.Lys1405Lys",
          "transcript": "NM_001406517.1",
          "protein_id": "NP_001393446.1",
          "transcript_support_level": null,
          "aa_start": 1405,
          "aa_end": null,
          "aa_length": 1433,
          "cds_start": 4215,
          "cds_end": null,
          "cds_length": 4302,
          "cdna_start": 4328,
          "cdna_end": null,
          "cdna_length": 6502,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 22,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4215G>A",
          "hgvs_p": "p.Lys1405Lys",
          "transcript": "NM_001406518.1",
          "protein_id": "NP_001393447.1",
          "transcript_support_level": null,
          "aa_start": 1405,
          "aa_end": null,
          "aa_length": 1433,
          "cds_start": 4215,
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          "cds_length": 4302,
          "cdna_start": 4515,
          "cdna_end": null,
          "cdna_length": 6689,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4176G>A",
          "hgvs_p": "p.Lys1392Lys",
          "transcript": "NM_001406519.1",
          "protein_id": "NP_001393448.1",
          "transcript_support_level": null,
          "aa_start": 1392,
          "aa_end": null,
          "aa_length": 1420,
          "cds_start": 4176,
          "cds_end": null,
          "cds_length": 4263,
          "cdna_start": 4289,
          "cdna_end": null,
          "cdna_length": 6463,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "K",
          "aa_alt": "K",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 21,
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      "splice_score_selected": 0.029999999329447746,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.7,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 2.374,
      "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": -20,
      "acmg_classification": "Benign",
      "acmg_criteria": "BP4_Strong,BP6_Very_Strong,BS1,BS2",
      "acmg_by_gene": [
        {
          "score": -20,
          "benign_score": 20,
          "pathogenic_score": 0,
          "criteria": [
            "BP4_Strong",
            "BP6_Very_Strong",
            "BS1",
            "BS2"
          ],
          "verdict": "Benign",
          "transcript": "ENST00000242839.10",
          "gene_symbol": "ATP7B",
          "hgnc_id": 870,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.4311G>A",
          "hgvs_p": "p.Lys1437Lys"
        }
      ],
      "clinvar_disease": "Inborn genetic diseases,Wilson disease,not provided,not specified",
      "clinvar_classification": "Benign/Likely benign",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "LB:5 B:8",
      "phenotype_combined": "Wilson disease|not specified|not provided|Inborn genetic diseases",
      "pathogenicity_classification_combined": "Benign/Likely benign",
      "custom_annotations": null
    }
  ],
  "message": null
}