← Back to variant description

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: 2-189008122-A-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=189008122&ref=A&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 0,
          "criteria": [
            "PVS1",
            "PM2"
          ],
          "effects": [
            "stop_gained"
          ],
          "gene_symbol": "COL3A1",
          "hgnc_id": 2201,
          "hgvs_c": "c.3505A>T",
          "hgvs_p": "p.Arg1169*",
          "inheritance_mode": "AD,AR",
          "pathogenic_score": 10,
          "score": 10,
          "transcript": "NM_000090.4",
          "verdict": "Pathogenic"
        },
        {
          "benign_score": 0,
          "criteria": [
            "PM2",
            "PP3_Strong"
          ],
          "effects": [
            "intron_variant"
          ],
          "gene_symbol": "ENSG00000295704",
          "hgnc_id": null,
          "hgvs_c": "n.178+773T>A",
          "hgvs_p": null,
          "inheritance_mode": "",
          "pathogenic_score": 6,
          "score": 6,
          "transcript": "ENST00000731902.1",
          "verdict": "Likely_pathogenic"
        }
      ],
      "acmg_classification": "Pathogenic",
      "acmg_criteria": "PVS1,PM2",
      "acmg_score": 10,
      "allele_count_reference_population": 0,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "T",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": "Pathogenic",
      "bayesdelnoaf_score": 0.58,
      "chr": "2",
      "clinvar_classification": "",
      "clinvar_disease": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "computational_prediction_selected": "Pathogenic",
      "computational_score_selected": 0.5799999833106995,
      "computational_source_selected": "BayesDel_noAF",
      "consequences": [
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 1466,
          "aa_ref": "R",
          "aa_start": 1169,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5490,
          "cdna_start": 3622,
          "cds_end": null,
          "cds_length": 4401,
          "cds_start": 3505,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 51,
          "exon_rank": 47,
          "exon_rank_end": null,
          "feature": "NM_000090.4",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "c.3505A>T",
          "hgvs_p": "p.Arg1169*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000304636.9",
          "protein_coding": true,
          "protein_id": "NP_000081.2",
          "strand": true,
          "transcript": "NM_000090.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 1466,
          "aa_ref": "R",
          "aa_start": 1169,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 5490,
          "cdna_start": 3622,
          "cds_end": null,
          "cds_length": 4401,
          "cds_start": 3505,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 51,
          "exon_rank": 47,
          "exon_rank_end": null,
          "feature": "ENST00000304636.9",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "c.3505A>T",
          "hgvs_p": "p.Arg1169*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_000090.4",
          "protein_coding": true,
          "protein_id": "ENSP00000304408.4",
          "strand": true,
          "transcript": "ENST00000304636.9",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 1433,
          "aa_ref": "R",
          "aa_start": 1136,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5391,
          "cdna_start": 3523,
          "cds_end": null,
          "cds_length": 4302,
          "cds_start": 3406,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 50,
          "exon_rank": 46,
          "exon_rank_end": null,
          "feature": "ENST00000450867.2",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "c.3406A>T",
          "hgvs_p": "p.Arg1136*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000415346.2",
          "strand": true,
          "transcript": "ENST00000450867.2",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 1463,
          "aa_ref": "R",
          "aa_start": 1166,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4787,
          "cdna_start": 3613,
          "cds_end": null,
          "cds_length": 4392,
          "cds_start": 3496,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 51,
          "exon_rank": 47,
          "exon_rank_end": null,
          "feature": "ENST00000879201.1",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "c.3496A>T",
          "hgvs_p": "p.Arg1166*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000549260.1",
          "strand": true,
          "transcript": "ENST00000879201.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 1451,
          "aa_ref": "R",
          "aa_start": 1154,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4757,
          "cdna_start": 3577,
          "cds_end": null,
          "cds_length": 4356,
          "cds_start": 3460,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 50,
          "exon_rank": 46,
          "exon_rank_end": null,
          "feature": "ENST00000879198.1",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "c.3460A>T",
          "hgvs_p": "p.Arg1154*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000549257.1",
          "strand": true,
          "transcript": "ENST00000879198.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 1449,
          "aa_ref": "R",
          "aa_start": 1152,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5436,
          "cdna_start": 3571,
          "cds_end": null,
          "cds_length": 4350,
          "cds_start": 3454,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 50,
          "exon_rank": 46,
          "exon_rank_end": null,
          "feature": "ENST00000879194.1",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "c.3454A>T",
          "hgvs_p": "p.Arg1152*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000549253.1",
          "strand": true,
          "transcript": "ENST00000879194.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 1448,
          "aa_ref": "R",
          "aa_start": 1151,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4742,
          "cdna_start": 3568,
          "cds_end": null,
          "cds_length": 4347,
          "cds_start": 3451,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 50,
          "exon_rank": 46,
          "exon_rank_end": null,
          "feature": "ENST00000879200.1",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "c.3451A>T",
          "hgvs_p": "p.Arg1151*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000549259.1",
          "strand": true,
          "transcript": "ENST00000879200.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 1448,
          "aa_ref": "R",
          "aa_start": 1151,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4669,
          "cdna_start": 3568,
          "cds_end": null,
          "cds_length": 4347,
          "cds_start": 3451,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 50,
          "exon_rank": 46,
          "exon_rank_end": null,
          "feature": "ENST00000879202.1",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "c.3451A>T",
          "hgvs_p": "p.Arg1151*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000549261.1",
          "strand": true,
          "transcript": "ENST00000879202.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 1448,
          "aa_ref": "R",
          "aa_start": 1151,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4743,
          "cdna_start": 3568,
          "cds_end": null,
          "cds_length": 4347,
          "cds_start": 3451,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 50,
          "exon_rank": 46,
          "exon_rank_end": null,
          "feature": "ENST00000957918.1",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "c.3451A>T",
          "hgvs_p": "p.Arg1151*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000627977.1",
          "strand": true,
          "transcript": "ENST00000957918.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 1433,
          "aa_ref": "R",
          "aa_start": 1136,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5388,
          "cdna_start": 3523,
          "cds_end": null,
          "cds_length": 4302,
          "cds_start": 3406,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 50,
          "exon_rank": 46,
          "exon_rank_end": null,
          "feature": "ENST00000879195.1",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "c.3406A>T",
          "hgvs_p": "p.Arg1136*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000549254.1",
          "strand": true,
          "transcript": "ENST00000879195.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 1430,
          "aa_ref": "R",
          "aa_start": 1133,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5376,
          "cdna_start": 3514,
          "cds_end": null,
          "cds_length": 4293,
          "cds_start": 3397,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 50,
          "exon_rank": 46,
          "exon_rank_end": null,
          "feature": "ENST00000879196.1",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "c.3397A>T",
          "hgvs_p": "p.Arg1133*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000549255.1",
          "strand": true,
          "transcript": "ENST00000879196.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 1430,
          "aa_ref": "R",
          "aa_start": 1133,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5349,
          "cdna_start": 3483,
          "cds_end": null,
          "cds_length": 4293,
          "cds_start": 3397,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 50,
          "exon_rank": 46,
          "exon_rank_end": null,
          "feature": "ENST00000879197.1",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "c.3397A>T",
          "hgvs_p": "p.Arg1133*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000549256.1",
          "strand": true,
          "transcript": "ENST00000879197.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 1430,
          "aa_ref": "R",
          "aa_start": 1133,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5382,
          "cdna_start": 3514,
          "cds_end": null,
          "cds_length": 4293,
          "cds_start": 3397,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 50,
          "exon_rank": 46,
          "exon_rank_end": null,
          "feature": "ENST00000957916.1",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "c.3397A>T",
          "hgvs_p": "p.Arg1133*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000627975.1",
          "strand": true,
          "transcript": "ENST00000957916.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 1426,
          "aa_ref": "R",
          "aa_start": 1169,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5369,
          "cdna_start": 3624,
          "cds_end": null,
          "cds_length": 4281,
          "cds_start": 3505,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 51,
          "exon_rank": 47,
          "exon_rank_end": null,
          "feature": "ENST00000957917.1",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "c.3505A>T",
          "hgvs_p": "p.Arg1169*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000627976.1",
          "strand": true,
          "transcript": "ENST00000957917.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 1425,
          "aa_ref": "R",
          "aa_start": 1128,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4428,
          "cdna_start": 3499,
          "cds_end": null,
          "cds_length": 4278,
          "cds_start": 3382,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 50,
          "exon_rank": 46,
          "exon_rank_end": null,
          "feature": "ENST00000879203.1",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "c.3382A>T",
          "hgvs_p": "p.Arg1128*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000549262.1",
          "strand": true,
          "transcript": "ENST00000879203.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 1418,
          "aa_ref": "R",
          "aa_start": 1121,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 4655,
          "cdna_start": 3478,
          "cds_end": null,
          "cds_length": 4257,
          "cds_start": 3361,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 49,
          "exon_rank": 45,
          "exon_rank_end": null,
          "feature": "ENST00000879199.1",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "c.3361A>T",
          "hgvs_p": "p.Arg1121*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000549258.1",
          "strand": true,
          "transcript": "ENST00000879199.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 1415,
          "aa_ref": "R",
          "aa_start": 1118,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5337,
          "cdna_start": 3469,
          "cds_end": null,
          "cds_length": 4248,
          "cds_start": 3352,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 49,
          "exon_rank": 45,
          "exon_rank_end": null,
          "feature": "ENST00000713745.1",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "c.3352A>T",
          "hgvs_p": "p.Arg1118*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000519049.1",
          "strand": true,
          "transcript": "ENST00000713745.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "*",
          "aa_end": null,
          "aa_length": 1412,
          "aa_ref": "R",
          "aa_start": 1115,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 5328,
          "cdna_start": 3460,
          "cds_end": null,
          "cds_length": 4239,
          "cds_start": 3343,
          "consequences": [
            "stop_gained"
          ],
          "exon_count": 49,
          "exon_rank": 45,
          "exon_rank_end": null,
          "feature": "ENST00000713744.1",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "c.3343A>T",
          "hgvs_p": "p.Arg1115*",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000519048.1",
          "strand": true,
          "transcript": "ENST00000713744.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "pseudogene",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 439,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "intron_variant"
          ],
          "exon_count": 3,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000731902.1",
          "gene_hgnc_id": null,
          "gene_symbol": "ENSG00000295704",
          "hgvs_c": "n.178+773T>A",
          "hgvs_p": null,
          "intron_rank": 1,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": false,
          "transcript": "ENST00000731902.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": null,
          "aa_end": null,
          "aa_length": null,
          "aa_ref": null,
          "aa_start": null,
          "biotype": "retained_intron",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 2054,
          "cdna_start": null,
          "cds_end": null,
          "cds_length": null,
          "cds_start": null,
          "consequences": [
            "upstream_gene_variant"
          ],
          "exon_count": 3,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000487010.1",
          "gene_hgnc_id": 2201,
          "gene_symbol": "COL3A1",
          "hgvs_c": "n.-180A>T",
          "hgvs_p": null,
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": false,
          "protein_id": null,
          "strand": true,
          "transcript": "ENST00000487010.1",
          "transcript_support_level": 2
        }
      ],
      "custom_annotations": null,
      "dbscsnv_ada_prediction": null,
      "dbscsnv_ada_score": null,
      "dbsnp": null,
      "effect": "stop_gained",
      "frequency_reference_population": null,
      "gene_hgnc_id": 2201,
      "gene_symbol": "COL3A1",
      "gnomad_exomes_ac": null,
      "gnomad_exomes_af": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_ac": null,
      "gnomad_genomes_af": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_heteroplasmic": null,
      "gnomad_mito_homoplasmic": null,
      "hom_count_reference_population": 0,
      "mitotip_prediction": null,
      "mitotip_score": null,
      "pathogenicity_classification_combined": null,
      "phenotype_combined": null,
      "phylop100way_prediction": "Benign",
      "phylop100way_score": 1.445,
      "pos": 189008122,
      "ref": "A",
      "revel_prediction": null,
      "revel_score": null,
      "splice_prediction_selected": "Benign",
      "splice_score_selected": 0.07000000029802322,
      "splice_source_selected": "max_spliceai",
      "spliceai_max_prediction": "Benign",
      "spliceai_max_score": 0.07,
      "transcript": "NM_000090.4"
    }
  ]
}
For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.