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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: 13-51935603-G-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=13&pos=51935603&ref=G&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "13",
      "pos": 51935603,
      "ref": "G",
      "alt": "A",
      "effect": "stop_gained",
      "transcript": "ENST00000242839.10",
      "consequences": [
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4114C>T",
          "hgvs_p": "p.Gln1372*",
          "transcript": "NM_000053.4",
          "protein_id": "NP_000044.2",
          "transcript_support_level": null,
          "aa_start": 1372,
          "aa_end": null,
          "aa_length": 1465,
          "cds_start": 4114,
          "cds_end": null,
          "cds_length": 4398,
          "cdna_start": 4227,
          "cdna_end": null,
          "cdna_length": 6598,
          "mane_select": "ENST00000242839.10",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4114C>T",
          "hgvs_p": "p.Gln1372*",
          "transcript": "ENST00000242839.10",
          "protein_id": "ENSP00000242839.5",
          "transcript_support_level": 1,
          "aa_start": 1372,
          "aa_end": null,
          "aa_length": 1465,
          "cds_start": 4114,
          "cds_end": null,
          "cds_length": 4398,
          "cdna_start": 4227,
          "cdna_end": null,
          "cdna_length": 6598,
          "mane_select": "NM_000053.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3970C>T",
          "hgvs_p": "p.Gln1324*",
          "transcript": "ENST00000634844.1",
          "protein_id": "ENSP00000489398.1",
          "transcript_support_level": 1,
          "aa_start": 1324,
          "aa_end": null,
          "aa_length": 1417,
          "cds_start": 3970,
          "cds_end": null,
          "cds_length": 4254,
          "cdna_start": 4044,
          "cdna_end": null,
          "cdna_length": 4398,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3919C>T",
          "hgvs_p": "p.Gln1307*",
          "transcript": "ENST00000418097.7",
          "protein_id": "ENSP00000393343.2",
          "transcript_support_level": 1,
          "aa_start": 1307,
          "aa_end": null,
          "aa_length": 1400,
          "cds_start": 3919,
          "cds_end": null,
          "cds_length": 4203,
          "cdna_start": 3993,
          "cdna_end": null,
          "cdna_length": 4340,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 18,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3862C>T",
          "hgvs_p": "p.Gln1288*",
          "transcript": "ENST00000448424.7",
          "protein_id": "ENSP00000416738.3",
          "transcript_support_level": 1,
          "aa_start": 1288,
          "aa_end": null,
          "aa_length": 1381,
          "cds_start": 3862,
          "cds_end": null,
          "cds_length": 4146,
          "cdna_start": 4115,
          "cdna_end": null,
          "cdna_length": 6451,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3781C>T",
          "hgvs_p": "p.Gln1261*",
          "transcript": "ENST00000400366.6",
          "protein_id": "ENSP00000383217.3",
          "transcript_support_level": 1,
          "aa_start": 1261,
          "aa_end": null,
          "aa_length": 1354,
          "cds_start": 3781,
          "cds_end": null,
          "cds_length": 4065,
          "cdna_start": 3781,
          "cdna_end": null,
          "cdna_length": 4065,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 12,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.2824C>T",
          "hgvs_p": "p.Gln942*",
          "transcript": "ENST00000400370.8",
          "protein_id": "ENSP00000383221.3",
          "transcript_support_level": 1,
          "aa_start": 942,
          "aa_end": null,
          "aa_length": 1035,
          "cds_start": 2824,
          "cds_end": null,
          "cds_length": 3108,
          "cdna_start": 2898,
          "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": 20,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.*1215C>T",
          "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": 16,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.4858C>T",
          "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": 13,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.3459C>T",
          "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": 20,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "n.*1215C>T",
          "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": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4114C>T",
          "hgvs_p": "p.Gln1372*",
          "transcript": "NM_001406511.1",
          "protein_id": "NP_001393440.1",
          "transcript_support_level": null,
          "aa_start": 1372,
          "aa_end": null,
          "aa_length": 1465,
          "cds_start": 4114,
          "cds_end": null,
          "cds_length": 4398,
          "cdna_start": 4281,
          "cdna_end": null,
          "cdna_length": 6652,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4114C>T",
          "hgvs_p": "p.Gln1372*",
          "transcript": "NM_001406512.1",
          "protein_id": "NP_001393441.1",
          "transcript_support_level": null,
          "aa_start": 1372,
          "aa_end": null,
          "aa_length": 1465,
          "cds_start": 4114,
          "cds_end": null,
          "cds_length": 4398,
          "cdna_start": 4520,
          "cdna_end": null,
          "cdna_length": 6891,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4108C>T",
          "hgvs_p": "p.Gln1370*",
          "transcript": "NM_001406513.1",
          "protein_id": "NP_001393442.1",
          "transcript_support_level": null,
          "aa_start": 1370,
          "aa_end": null,
          "aa_length": 1463,
          "cds_start": 4108,
          "cds_end": null,
          "cds_length": 4392,
          "cdna_start": 4275,
          "cdna_end": null,
          "cdna_length": 6646,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4081C>T",
          "hgvs_p": "p.Gln1361*",
          "transcript": "NM_001406514.1",
          "protein_id": "NP_001393443.1",
          "transcript_support_level": null,
          "aa_start": 1361,
          "aa_end": null,
          "aa_length": 1454,
          "cds_start": 4081,
          "cds_end": null,
          "cds_length": 4365,
          "cdna_start": 4194,
          "cdna_end": null,
          "cdna_length": 6565,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4060C>T",
          "hgvs_p": "p.Gln1354*",
          "transcript": "NM_001406515.1",
          "protein_id": "NP_001393444.1",
          "transcript_support_level": null,
          "aa_start": 1354,
          "aa_end": null,
          "aa_length": 1447,
          "cds_start": 4060,
          "cds_end": null,
          "cds_length": 4344,
          "cdna_start": 4173,
          "cdna_end": null,
          "cdna_length": 6544,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4060C>T",
          "hgvs_p": "p.Gln1354*",
          "transcript": "NM_001406516.1",
          "protein_id": "NP_001393445.1",
          "transcript_support_level": null,
          "aa_start": 1354,
          "aa_end": null,
          "aa_length": 1447,
          "cds_start": 4060,
          "cds_end": null,
          "cds_length": 4344,
          "cdna_start": 4466,
          "cdna_end": null,
          "cdna_length": 6837,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4018C>T",
          "hgvs_p": "p.Gln1340*",
          "transcript": "NM_001406517.1",
          "protein_id": "NP_001393446.1",
          "transcript_support_level": null,
          "aa_start": 1340,
          "aa_end": null,
          "aa_length": 1433,
          "cds_start": 4018,
          "cds_end": null,
          "cds_length": 4302,
          "cdna_start": 4131,
          "cdna_end": null,
          "cdna_length": 6502,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 22,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.4018C>T",
          "hgvs_p": "p.Gln1340*",
          "transcript": "NM_001406518.1",
          "protein_id": "NP_001393447.1",
          "transcript_support_level": null,
          "aa_start": 1340,
          "aa_end": null,
          "aa_length": 1433,
          "cds_start": 4018,
          "cds_end": null,
          "cds_length": 4302,
          "cdna_start": 4318,
          "cdna_end": null,
          "cdna_length": 6689,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 19,
          "exon_rank_end": null,
          "exon_count": 20,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "ATP7B",
          "gene_hgnc_id": 870,
          "hgvs_c": "c.3979C>T",
          "hgvs_p": "p.Gln1327*",
          "transcript": "NM_001406519.1",
          "protein_id": "NP_001393448.1",
          "transcript_support_level": null,
          "aa_start": 1327,
          "aa_end": null,
          "aa_length": 1420,
          "cds_start": 3979,
          "cds_end": null,
          "cds_length": 4263,
          "cdna_start": 4092,
          "cdna_end": null,
          "cdna_length": 6463,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "Q",
          "aa_alt": "*",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "stop_gained"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 21,
          "intron_rank": null,
          "intron_rank_end": null,
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      "bayesdelnoaf_score": 0.56,
      "bayesdelnoaf_prediction": "Pathogenic",
      "phylop100way_score": 6.386,
      "phylop100way_prediction": "Uncertain_significance",
      "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": 18,
      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1,PM2,PP5_Very_Strong",
      "acmg_by_gene": [
        {
          "score": 18,
          "benign_score": 0,
          "pathogenic_score": 18,
          "criteria": [
            "PVS1",
            "PM2",
            "PP5_Very_Strong"
          ],
          "verdict": "Pathogenic",
          "transcript": "ENST00000242839.10",
          "gene_symbol": "ATP7B",
          "hgnc_id": 870,
          "effects": [
            "stop_gained"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.4114C>T",
          "hgvs_p": "p.Gln1372*"
        }
      ],
      "clinvar_disease": "Wilson disease",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "criteria provided, multiple submitters, no conflicts",
      "clinvar_submissions_summary": "P:4",
      "phenotype_combined": "Wilson disease",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}