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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: 12-18699791-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=18699791&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "12",
      "pos": 18699791,
      "ref": "T",
      "alt": "C",
      "effect": "splice_region_variant,intron_variant",
      "transcript": "NM_033123.4",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "PLCZ1",
          "gene_hgnc_id": 19218,
          "hgvs_c": "c.1174+3A>G",
          "hgvs_p": null,
          "transcript": "NM_033123.4",
          "protein_id": "NP_149114.2",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 608,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1827,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2105,
          "mane_select": "ENST00000266505.12",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "PLCZ1",
          "gene_hgnc_id": 19218,
          "hgvs_c": "c.1174+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000266505.12",
          "protein_id": "ENSP00000266505.7",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 608,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1827,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2105,
          "mane_select": "NM_033123.4",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "PLCZ1",
          "gene_hgnc_id": 19218,
          "hgvs_c": "c.1297+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000648272.1",
          "protein_id": "ENSP00000497636.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 649,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1950,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2320,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "PLCZ1",
          "gene_hgnc_id": 19218,
          "hgvs_c": "c.595+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000539875.5",
          "protein_id": "ENSP00000445026.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 415,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1248,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1398,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "PLCZ1",
          "gene_hgnc_id": 19218,
          "hgvs_c": "n.*1039+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000318197.10",
          "protein_id": "ENSP00000326397.6",
          "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": 2113,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 15,
          "intron_rank": 10,
          "intron_rank_end": null,
          "gene_symbol": "PLCZ1",
          "gene_hgnc_id": 19218,
          "hgvs_c": "c.862+3A>G",
          "hgvs_p": null,
          "transcript": "NM_001330774.2",
          "protein_id": "NP_001317703.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 504,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1515,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2108,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "PLCZ1",
          "gene_hgnc_id": 19218,
          "hgvs_c": "c.595+3A>G",
          "hgvs_p": null,
          "transcript": "NM_001330769.1",
          "protein_id": "NP_001317698.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 415,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1248,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1445,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "PLCZ1",
          "gene_hgnc_id": 19218,
          "hgvs_c": "c.520+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000538330.5",
          "protein_id": "ENSP00000445880.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 390,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1173,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1612,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "PLCZ1",
          "gene_hgnc_id": 19218,
          "hgvs_c": "c.379+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000540421.5",
          "protein_id": "ENSP00000445889.1",
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 264,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 797,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 797,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "PLCZ1",
          "gene_hgnc_id": 19218,
          "hgvs_c": "n.787+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000540270.5",
          "protein_id": "ENSP00000443320.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 1667,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PLCZ1",
          "gene_hgnc_id": 19218,
          "hgvs_c": "n.247+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000540515.1",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 323,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "PLCZ1",
          "gene_hgnc_id": 19218,
          "hgvs_c": "n.697+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000542762.5",
          "protein_id": null,
          "transcript_support_level": 3,
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          "aa_length": null,
          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 814,
          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
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          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 33,
          "intron_rank": 32,
          "intron_rank_end": null,
          "gene_symbol": "PIK3C2G",
          "gene_hgnc_id": 8973,
          "hgvs_c": "c.4309-15895T>C",
          "hgvs_p": null,
          "transcript": "XM_017019471.2",
          "protein_id": "XP_016874960.1",
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          "aa_start": null,
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          "aa_length": 1492,
          "cds_start": -4,
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          "cds_length": 4479,
          "cdna_start": null,
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        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 33,
          "intron_rank": 32,
          "intron_rank_end": null,
          "gene_symbol": "PIK3C2G",
          "gene_hgnc_id": 8973,
          "hgvs_c": "c.4309-15895T>C",
          "hgvs_p": null,
          "transcript": "XM_017019473.3",
          "protein_id": "XP_016874962.1",
          "transcript_support_level": null,
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          "aa_length": 1492,
          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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        {
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          ],
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          "gene_symbol": "PIK3C2G",
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          "hgvs_c": "c.4309-15895T>C",
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          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 32,
          "intron_rank": 31,
          "intron_rank_end": null,
          "gene_symbol": "PIK3C2G",
          "gene_hgnc_id": 8973,
          "hgvs_c": "c.4186-15895T>C",
          "hgvs_p": null,
          "transcript": "XM_047429008.1",
          "protein_id": "XP_047284964.1",
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          "cds_start": -4,
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          "mane_select": null,
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        },
        {
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          "canonical": false,
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          "exon_rank": null,
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          "exon_count": 20,
          "intron_rank": 19,
          "intron_rank_end": null,
          "gene_symbol": "PIK3C2G",
          "gene_hgnc_id": 8973,
          "hgvs_c": "c.2284-15895T>C",
          "hgvs_p": null,
          "transcript": "XM_017019479.2",
          "protein_id": "XP_016874968.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 817,
          "cds_start": -4,
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          "cds_length": 2454,
          "cdna_start": null,
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          "mane_select": null,
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          "feature": null
        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 15,
          "intron_rank": 9,
          "intron_rank_end": null,
          "gene_symbol": "PLCZ1",
          "gene_hgnc_id": 19218,
          "hgvs_c": "c.1297+3A>G",
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          "transcript": "XM_017020176.2",
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          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 16,
          "intron_rank": 10,
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          "gene_symbol": "PLCZ1",
          "gene_hgnc_id": 19218,
          "hgvs_c": "c.1174+3A>G",
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          "transcript": "XM_017020177.2",
          "protein_id": "XP_016875666.1",
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          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 2091,
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          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
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          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 14,
          "intron_rank": 8,
          "intron_rank_end": null,
          "gene_symbol": "PLCZ1",
          "gene_hgnc_id": 19218,
          "hgvs_c": "c.1147+3A>G",
          "hgvs_p": null,
          "transcript": "XM_017020178.2",
          "protein_id": "XP_016875667.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 609,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1830,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2064,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 12,
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      "acmg_by_gene": [
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          "verdict": "Uncertain_significance",
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        {
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          "verdict": "Uncertain_significance",
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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
}