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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: 12-8932728-CGCAGCAGCA-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=8932728&ref=CGCAGCAGCA&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "12",
      "pos": 8932728,
      "ref": "CGCAGCAGCA",
      "alt": "C",
      "effect": "disruptive_inframe_deletion",
      "transcript": "ENST00000544916.6",
      "consequences": [
        {
          "aa_ref": "QQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "c.1281_1289delGCAGCAGCA",
          "hgvs_p": "p.Gln428_Gln430del",
          "transcript": "NM_004426.3",
          "protein_id": "NP_004417.2",
          "transcript_support_level": null,
          "aa_start": 427,
          "aa_end": null,
          "aa_length": 1004,
          "cds_start": 1281,
          "cds_end": null,
          "cds_length": 3015,
          "cdna_start": 1648,
          "cdna_end": null,
          "cdna_length": 5390,
          "mane_select": "ENST00000544916.6",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQ",
          "aa_alt": "Q",
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "c.1281_1289delGCAGCAGCA",
          "hgvs_p": "p.Gln428_Gln430del",
          "transcript": "ENST00000544916.6",
          "protein_id": "ENSP00000437659.1",
          "transcript_support_level": 1,
          "aa_start": 427,
          "aa_end": null,
          "aa_length": 1004,
          "cds_start": 1281,
          "cds_end": null,
          "cds_length": 3015,
          "cdna_start": 1648,
          "cdna_end": null,
          "cdna_length": 5390,
          "mane_select": "NM_004426.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "c.1281_1289delGCAGCAGCA",
          "hgvs_p": "p.Gln428_Gln430del",
          "transcript": "ENST00000543824.5",
          "protein_id": "ENSP00000440674.1",
          "transcript_support_level": 1,
          "aa_start": 427,
          "aa_end": null,
          "aa_length": 1004,
          "cds_start": 1281,
          "cds_end": null,
          "cds_length": 3015,
          "cdna_start": 1613,
          "cdna_end": null,
          "cdna_length": 4292,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "c.1146_1154delGCAGCAGCA",
          "hgvs_p": "p.Gln383_Gln385del",
          "transcript": "ENST00000433083.6",
          "protein_id": "ENSP00000399194.2",
          "transcript_support_level": 1,
          "aa_start": 382,
          "aa_end": null,
          "aa_length": 959,
          "cds_start": 1146,
          "cds_end": null,
          "cds_length": 2880,
          "cdna_start": 1291,
          "cdna_end": null,
          "cdna_length": 5033,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "n.*650_*658delGCAGCAGCA",
          "hgvs_p": null,
          "transcript": "ENST00000540574.5",
          "protein_id": "ENSP00000444308.1",
          "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": 3869,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "n.*650_*658delGCAGCAGCA",
          "hgvs_p": null,
          "transcript": "ENST00000540574.5",
          "protein_id": "ENSP00000444308.1",
          "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": 3869,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "c.1281_1289delGCAGCAGCA",
          "hgvs_p": "p.Gln428_Gln430del",
          "transcript": "NM_001413738.1",
          "protein_id": "NP_001400667.1",
          "transcript_support_level": null,
          "aa_start": 427,
          "aa_end": null,
          "aa_length": 1004,
          "cds_start": 1281,
          "cds_end": null,
          "cds_length": 3015,
          "cdna_start": 1437,
          "cdna_end": null,
          "cdna_length": 5179,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "c.1275_1283delGCAGCAGCA",
          "hgvs_p": "p.Gln426_Gln428del",
          "transcript": "NM_001413739.1",
          "protein_id": "NP_001400668.1",
          "transcript_support_level": null,
          "aa_start": 425,
          "aa_end": null,
          "aa_length": 1002,
          "cds_start": 1275,
          "cds_end": null,
          "cds_length": 3009,
          "cdna_start": 1642,
          "cdna_end": null,
          "cdna_length": 5384,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "c.1257_1265delGCAGCAGCA",
          "hgvs_p": "p.Gln420_Gln422del",
          "transcript": "NM_001413740.1",
          "protein_id": "NP_001400669.1",
          "transcript_support_level": null,
          "aa_start": 419,
          "aa_end": null,
          "aa_length": 996,
          "cds_start": 1257,
          "cds_end": null,
          "cds_length": 2991,
          "cdna_start": 1624,
          "cdna_end": null,
          "cdna_length": 5366,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "c.1170_1178delGCAGCAGCA",
          "hgvs_p": "p.Gln391_Gln393del",
          "transcript": "NM_001413741.1",
          "protein_id": "NP_001400670.1",
          "transcript_support_level": null,
          "aa_start": 390,
          "aa_end": null,
          "aa_length": 967,
          "cds_start": 1170,
          "cds_end": null,
          "cds_length": 2904,
          "cdna_start": 1537,
          "cdna_end": null,
          "cdna_length": 5279,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "c.1125_1133delGCAGCAGCA",
          "hgvs_p": "p.Gln376_Gln378del",
          "transcript": "NM_001413742.1",
          "protein_id": "NP_001400671.1",
          "transcript_support_level": null,
          "aa_start": 375,
          "aa_end": null,
          "aa_length": 952,
          "cds_start": 1125,
          "cds_end": null,
          "cds_length": 2859,
          "cdna_start": 1281,
          "cdna_end": null,
          "cdna_length": 5023,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "c.1125_1133delGCAGCAGCA",
          "hgvs_p": "p.Gln376_Gln378del",
          "transcript": "NM_001413743.1",
          "protein_id": "NP_001400672.1",
          "transcript_support_level": null,
          "aa_start": 375,
          "aa_end": null,
          "aa_length": 952,
          "cds_start": 1125,
          "cds_end": null,
          "cds_length": 2859,
          "cdna_start": 1492,
          "cdna_end": null,
          "cdna_length": 5234,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "c.1281_1289delGCAGCAGCA",
          "hgvs_p": "p.Gln428_Gln430del",
          "transcript": "NM_001413744.1",
          "protein_id": "NP_001400673.1",
          "transcript_support_level": null,
          "aa_start": 427,
          "aa_end": null,
          "aa_length": 879,
          "cds_start": 1281,
          "cds_end": null,
          "cds_length": 2640,
          "cdna_start": 1648,
          "cdna_end": null,
          "cdna_length": 5015,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "c.1281_1289delGCAGCAGCA",
          "hgvs_p": "p.Gln428_Gln430del",
          "transcript": "NM_001413745.1",
          "protein_id": "NP_001400674.1",
          "transcript_support_level": null,
          "aa_start": 427,
          "aa_end": null,
          "aa_length": 863,
          "cds_start": 1281,
          "cds_end": null,
          "cds_length": 2592,
          "cdna_start": 1648,
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          "cdna_length": 4967,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 16,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "c.1281_1289delGCAGCAGCA",
          "hgvs_p": "p.Gln428_Gln430del",
          "transcript": "NM_001413746.1",
          "protein_id": "NP_001400675.1",
          "transcript_support_level": null,
          "aa_start": 427,
          "aa_end": null,
          "aa_length": 857,
          "cds_start": 1281,
          "cds_end": null,
          "cds_length": 2574,
          "cdna_start": 1648,
          "cdna_end": null,
          "cdna_length": 4949,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "c.1281_1289delGCAGCAGCA",
          "hgvs_p": "p.Gln428_Gln430del",
          "transcript": "NM_001413747.1",
          "protein_id": "NP_001400676.1",
          "transcript_support_level": null,
          "aa_start": 427,
          "aa_end": null,
          "aa_length": 831,
          "cds_start": 1281,
          "cds_end": null,
          "cds_length": 2496,
          "cdna_start": 1648,
          "cdna_end": null,
          "cdna_length": 4871,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "c.1281_1289delGCAGCAGCA",
          "hgvs_p": "p.Gln428_Gln430del",
          "transcript": "NM_001413748.1",
          "protein_id": "NP_001400677.1",
          "transcript_support_level": null,
          "aa_start": 427,
          "aa_end": null,
          "aa_length": 825,
          "cds_start": 1281,
          "cds_end": null,
          "cds_length": 2478,
          "cdna_start": 1437,
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          "cdna_length": 4642,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "c.1281_1289delGCAGCAGCA",
          "hgvs_p": "p.Gln428_Gln430del",
          "transcript": "NM_001413749.1",
          "protein_id": "NP_001400678.1",
          "transcript_support_level": null,
          "aa_start": 427,
          "aa_end": null,
          "aa_length": 825,
          "cds_start": 1281,
          "cds_end": null,
          "cds_length": 2478,
          "cdna_start": 1648,
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          "cdna_length": 4853,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "c.1257_1265delGCAGCAGCA",
          "hgvs_p": "p.Gln420_Gln422del",
          "transcript": "NM_001413750.1",
          "protein_id": "NP_001400679.1",
          "transcript_support_level": null,
          "aa_start": 419,
          "aa_end": null,
          "aa_length": 823,
          "cds_start": 1257,
          "cds_end": null,
          "cds_length": 2472,
          "cdna_start": 1624,
          "cdna_end": null,
          "cdna_length": 4847,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": "QQQQ",
          "aa_alt": "Q",
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "disruptive_inframe_deletion"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "PHC1",
          "gene_hgnc_id": 3182,
          "hgvs_c": "c.1257_1265delGCAGCAGCA",
          "hgvs_p": "p.Gln420_Gln422del",
          "transcript": "NM_001413751.1",
          "protein_id": "NP_001400680.1",
          "transcript_support_level": null,
          "aa_start": 419,
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      "bayesdelnoaf_score": null,
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          "benign_score": 0,
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      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
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  "message": null
}