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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: 1-149003009-GCT-ACA (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=149003009&ref=GCT&alt=ACA&genome=hg38&allGenes=true"

API Response

json
{
  "message": null,
  "variants": [
    {
      "acmg_by_gene": [
        {
          "benign_score": 0,
          "criteria": [],
          "effects": [
            "missense_variant"
          ],
          "gene_symbol": "PDE4DIP",
          "hgnc_id": 15580,
          "hgvs_c": "c.4222_4224delGCTinsACA",
          "hgvs_p": "p.Ala1408Thr",
          "inheritance_mode": "AR",
          "pathogenic_score": 0,
          "score": 0,
          "transcript": "NM_001395297.1",
          "verdict": "Uncertain_significance"
        }
      ],
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "",
      "acmg_score": 0,
      "allele_count_reference_population": 0,
      "alphamissense_prediction": null,
      "alphamissense_score": null,
      "alt": "ACA",
      "apogee2_prediction": null,
      "apogee2_score": null,
      "bayesdelnoaf_prediction": null,
      "bayesdelnoaf_score": null,
      "chr": "1",
      "clinvar_classification": "",
      "clinvar_disease": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "computational_prediction_selected": null,
      "computational_score_selected": null,
      "computational_source_selected": null,
      "consequences": [
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2412,
          "aa_ref": "A",
          "aa_start": 1311,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8617,
          "cdna_start": 4278,
          "cds_end": null,
          "cds_length": 7239,
          "cds_start": 3931,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 47,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001395426.1",
          "gene_hgnc_id": 15580,
          "gene_symbol": "PDE4DIP",
          "hgvs_c": "c.3931_3933delGCTinsACA",
          "hgvs_p": "p.Ala1311Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "ENST00000695795.1",
          "protein_coding": true,
          "protein_id": "NP_001382355.1",
          "strand": true,
          "transcript": "NM_001395426.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2412,
          "aa_ref": "A",
          "aa_start": 1311,
          "biotype": "protein_coding",
          "canonical": true,
          "cdna_end": null,
          "cdna_length": 8617,
          "cdna_start": 4278,
          "cds_end": null,
          "cds_length": 7239,
          "cds_start": 3931,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 47,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000695795.1",
          "gene_hgnc_id": 15580,
          "gene_symbol": "PDE4DIP",
          "hgvs_c": "c.3931_3933delGCTinsACA",
          "hgvs_p": "p.Ala1311Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": "NM_001395426.1",
          "protein_coding": true,
          "protein_id": "ENSP00000512175.1",
          "strand": true,
          "transcript": "ENST00000695795.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2362,
          "aa_ref": "A",
          "aa_start": 1245,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8307,
          "cdna_start": 4024,
          "cds_end": null,
          "cds_length": 7089,
          "cds_start": 3733,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 44,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000369356.8",
          "gene_hgnc_id": 15580,
          "gene_symbol": "PDE4DIP",
          "hgvs_c": "c.3733_3735delGCTinsACA",
          "hgvs_p": "p.Ala1245Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000358363.4",
          "strand": true,
          "transcript": "ENST00000369356.8",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2346,
          "aa_ref": "A",
          "aa_start": 1245,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8262,
          "cdna_start": 3923,
          "cds_end": null,
          "cds_length": 7041,
          "cds_start": 3733,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 44,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000369354.7",
          "gene_hgnc_id": 15580,
          "gene_symbol": "PDE4DIP",
          "hgvs_c": "c.3733_3735delGCTinsACA",
          "hgvs_p": "p.Ala1245Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000358360.3",
          "strand": true,
          "transcript": "ENST00000369354.7",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2240,
          "aa_ref": "A",
          "aa_start": 1201,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8150,
          "cdna_start": 3994,
          "cds_end": null,
          "cds_length": 6723,
          "cds_start": 3601,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 46,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000618462.4",
          "gene_hgnc_id": 15580,
          "gene_symbol": "PDE4DIP",
          "hgvs_c": "c.3601_3603delGCTinsACA",
          "hgvs_p": "p.Ala1201Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000479409.1",
          "strand": true,
          "transcript": "ENST00000618462.4",
          "transcript_support_level": 1
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2525,
          "aa_ref": "A",
          "aa_start": 1408,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8912,
          "cdna_start": 4629,
          "cds_end": null,
          "cds_length": 7578,
          "cds_start": 4222,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 40,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001395297.1",
          "gene_hgnc_id": 15580,
          "gene_symbol": "PDE4DIP",
          "hgvs_c": "c.4222_4224delGCTinsACA",
          "hgvs_p": "p.Ala1408Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001382226.1",
          "strand": true,
          "transcript": "NM_001395297.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2508,
          "aa_ref": "A",
          "aa_start": 1408,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8965,
          "cdna_start": 4629,
          "cds_end": null,
          "cds_length": 7527,
          "cds_start": 4222,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 40,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001350520.2",
          "gene_hgnc_id": 15580,
          "gene_symbol": "PDE4DIP",
          "hgvs_c": "c.4222_4224delGCTinsACA",
          "hgvs_p": "p.Ala1408Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001337449.1",
          "strand": true,
          "transcript": "NM_001350520.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2508,
          "aa_ref": "A",
          "aa_start": 1408,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 9377,
          "cdna_start": 5050,
          "cds_end": null,
          "cds_length": 7527,
          "cds_start": 4222,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 40,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000704840.1",
          "gene_hgnc_id": 15580,
          "gene_symbol": "PDE4DIP",
          "hgvs_c": "c.4222_4224delGCTinsACA",
          "hgvs_p": "p.Ala1408Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000516056.1",
          "strand": true,
          "transcript": "ENST00000704840.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2483,
          "aa_ref": "A",
          "aa_start": 1382,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8554,
          "cdna_start": 4215,
          "cds_end": null,
          "cds_length": 7452,
          "cds_start": 4144,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 47,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001377392.2",
          "gene_hgnc_id": 15580,
          "gene_symbol": "PDE4DIP",
          "hgvs_c": "c.4144_4146delGCTinsACA",
          "hgvs_p": "p.Ala1382Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001364321.1",
          "strand": true,
          "transcript": "NM_001377392.2",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2483,
          "aa_ref": "A",
          "aa_start": 1382,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8554,
          "cdna_start": 4215,
          "cds_end": null,
          "cds_length": 7452,
          "cds_start": 4144,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 47,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000695794.1",
          "gene_hgnc_id": 15580,
          "gene_symbol": "PDE4DIP",
          "hgvs_c": "c.4144_4146delGCTinsACA",
          "hgvs_p": "p.Ala1382Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000512174.1",
          "strand": true,
          "transcript": "ENST00000695794.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2482,
          "aa_ref": "A",
          "aa_start": 1382,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8551,
          "cdna_start": 4215,
          "cds_end": null,
          "cds_length": 7449,
          "cds_start": 4144,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 47,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001395298.1",
          "gene_hgnc_id": 15580,
          "gene_symbol": "PDE4DIP",
          "hgvs_c": "c.4144_4146delGCTinsACA",
          "hgvs_p": "p.Ala1382Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001382227.1",
          "strand": true,
          "transcript": "NM_001395298.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2482,
          "aa_ref": "A",
          "aa_start": 1382,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8439,
          "cdna_start": 4164,
          "cds_end": null,
          "cds_length": 7449,
          "cds_start": 4144,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 47,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000585156.5",
          "gene_hgnc_id": 15580,
          "gene_symbol": "PDE4DIP",
          "hgvs_c": "c.4144_4146delGCTinsACA",
          "hgvs_p": "p.Ala1382Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000462316.2",
          "strand": true,
          "transcript": "ENST00000585156.5",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2462,
          "aa_ref": "A",
          "aa_start": 1408,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8723,
          "cdna_start": 4629,
          "cds_end": null,
          "cds_length": 7389,
          "cds_start": 4222,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 39,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001395299.1",
          "gene_hgnc_id": 15580,
          "gene_symbol": "PDE4DIP",
          "hgvs_c": "c.4222_4224delGCTinsACA",
          "hgvs_p": "p.Ala1408Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001382228.1",
          "strand": true,
          "transcript": "NM_001395299.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2460,
          "aa_ref": "A",
          "aa_start": 1382,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8381,
          "cdna_start": 4215,
          "cds_end": null,
          "cds_length": 7383,
          "cds_start": 4144,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 46,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001350521.4",
          "gene_hgnc_id": 15580,
          "gene_symbol": "PDE4DIP",
          "hgvs_c": "c.4144_4146delGCTinsACA",
          "hgvs_p": "p.Ala1382Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001337450.1",
          "strand": true,
          "transcript": "NM_001350521.4",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2446,
          "aa_ref": "A",
          "aa_start": 1345,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8443,
          "cdna_start": 4104,
          "cds_end": null,
          "cds_length": 7341,
          "cds_start": 4033,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 46,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001395300.1",
          "gene_hgnc_id": 15580,
          "gene_symbol": "PDE4DIP",
          "hgvs_c": "c.4033_4035delGCTinsACA",
          "hgvs_p": "p.Ala1345Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001382229.1",
          "strand": true,
          "transcript": "NM_001395300.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2431,
          "aa_ref": "A",
          "aa_start": 1382,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8305,
          "cdna_start": 4183,
          "cds_end": null,
          "cds_length": 7296,
          "cds_start": 4144,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 46,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "ENST00000524974.5",
          "gene_hgnc_id": 15580,
          "gene_symbol": "PDE4DIP",
          "hgvs_c": "c.4144_4146delGCTinsACA",
          "hgvs_p": "p.Ala1382Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "ENSP00000480806.1",
          "strand": true,
          "transcript": "ENST00000524974.5",
          "transcript_support_level": 5
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2428,
          "aa_ref": "A",
          "aa_start": 1408,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8725,
          "cdna_start": 4629,
          "cds_end": null,
          "cds_length": 7287,
          "cds_start": 4222,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 39,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001395301.1",
          "gene_hgnc_id": 15580,
          "gene_symbol": "PDE4DIP",
          "hgvs_c": "c.4222_4224delGCTinsACA",
          "hgvs_p": "p.Ala1408Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001382230.1",
          "strand": true,
          "transcript": "NM_001395301.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2382,
          "aa_ref": "A",
          "aa_start": 1345,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8147,
          "cdna_start": 4104,
          "cds_end": null,
          "cds_length": 7149,
          "cds_start": 4033,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 45,
          "exon_rank": null,
          "exon_rank_end": null,
          "feature": "NM_001395302.1",
          "gene_hgnc_id": 15580,
          "gene_symbol": "PDE4DIP",
          "hgvs_c": "c.4033_4035delGCTinsACA",
          "hgvs_p": "p.Ala1345Thr",
          "intron_rank": null,
          "intron_rank_end": null,
          "mane_plus": null,
          "mane_select": null,
          "protein_coding": true,
          "protein_id": "NP_001382231.1",
          "strand": true,
          "transcript": "NM_001395302.1",
          "transcript_support_level": null
        },
        {
          "aa_alt": "T",
          "aa_end": null,
          "aa_length": 2382,
          "aa_ref": "A",
          "aa_start": 1345,
          "biotype": "protein_coding",
          "canonical": false,
          "cdna_end": null,
          "cdna_length": 8418,
          "cdna_start": 4398,
          "cds_end": null,
          "cds_length": 7149,
          "cds_start": 4033,
          "consequences": [
            "missense_variant"
          ],
          "exon_count": 45,
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}
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.