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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: X-123613636-T-C (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=123613636&ref=T&alt=C&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "X",
      "pos": 123613636,
      "ref": "T",
      "alt": "C",
      "effect": "splice_region_variant,intron_variant",
      "transcript": "NM_001081550.2",
      "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": 39,
          "intron_rank": 35,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "c.4519+3A>G",
          "hgvs_p": null,
          "transcript": "NM_001081550.2",
          "protein_id": "NP_001075019.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1593,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4782,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5600,
          "mane_select": "ENST00000245838.13",
          "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": 39,
          "intron_rank": 35,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "c.4519+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000245838.13",
          "protein_id": "ENSP00000245838.8",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1593,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4782,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5600,
          "mane_select": "NM_001081550.2",
          "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": 39,
          "intron_rank": 35,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "c.4519+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000355725.8",
          "protein_id": "ENSP00000347959.4",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1593,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4782,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4930,
          "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": 34,
          "intron_rank": 31,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "c.4174+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000491737.5",
          "protein_id": "ENSP00000419795.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1478,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4437,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4452,
          "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": 7,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "c.982+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000618150.4",
          "protein_id": "ENSP00000480478.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 414,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1245,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3211,
          "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": 10,
          "intron_rank": 6,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "c.901+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000441692.5",
          "protein_id": "ENSP00000415211.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 387,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1164,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4364,
          "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": 9,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "c.304+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000448128.5",
          "protein_id": "ENSP00000397317.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 188,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 567,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1365,
          "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": 8,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "c.286+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000416618.5",
          "protein_id": "ENSP00000415244.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 180,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 543,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 657,
          "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": 9,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "n.*761+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000432353.5",
          "protein_id": "ENSP00000415947.1",
          "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": 3188,
          "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": 39,
          "intron_rank": 35,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "c.4600+3A>G",
          "hgvs_p": null,
          "transcript": "NM_001441235.1",
          "protein_id": "NP_001428164.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1620,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4863,
          "cdna_start": null,
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          "cdna_length": 5681,
          "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": 39,
          "intron_rank": 35,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "c.4519+3A>G",
          "hgvs_p": null,
          "transcript": "NM_001441236.1",
          "protein_id": "NP_001428165.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1593,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4782,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8010,
          "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": 6,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "n.727+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000464992.6",
          "protein_id": null,
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 902,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 2,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "n.102+416A>G",
          "hgvs_p": null,
          "transcript": "ENST00000492203.1",
          "protein_id": null,
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
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          "cdna_start": null,
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          "mane_select": null,
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          "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": 4,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "n.986+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000496830.1",
          "protein_id": null,
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 1013,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
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          "consequences": [
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            "intron_variant"
          ],
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          "exon_count": 8,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "n.357+3A>G",
          "hgvs_p": null,
          "transcript": "ENST00000497887.5",
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          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
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          "cds_start": -4,
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          "cdna_start": null,
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          "cdna_length": 768,
          "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": 40,
          "intron_rank": 36,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "c.4678+3A>G",
          "hgvs_p": null,
          "transcript": "XM_047442263.1",
          "protein_id": "XP_047298219.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1646,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4941,
          "cdna_start": null,
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          "cdna_length": 5759,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": 36,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "c.4678+3A>G",
          "hgvs_p": null,
          "transcript": "XM_047442264.1",
          "protein_id": "XP_047298220.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "cds_start": -4,
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          "cds_length": 4941,
          "cdna_start": null,
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          "cdna_length": 8169,
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          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 40,
          "intron_rank": 36,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "c.4678+3A>G",
          "hgvs_p": null,
          "transcript": "XM_047442265.1",
          "protein_id": "XP_047298221.1",
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          "cdna_start": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 40,
          "intron_rank": 36,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
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          "hgvs_c": "c.4678+3A>G",
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          "transcript": "XM_047442266.1",
          "protein_id": "XP_047298222.1",
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          "cdna_start": null,
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          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 40,
          "intron_rank": 36,
          "intron_rank_end": null,
          "gene_symbol": "THOC2",
          "gene_hgnc_id": 19073,
          "hgvs_c": "c.4666+3A>G",
          "hgvs_p": null,
          "transcript": "XM_047442267.1",
          "protein_id": "XP_047298223.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 1642,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 4929,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 5747,
          "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,
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      ],
      "gene_symbol": "THOC2",
      "gene_hgnc_id": 19073,
      "dbsnp": "rs2046785257",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": null,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": null,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": null,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.3100000023841858,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0.9739999771118164,
      "splice_prediction_selected": "Pathogenic",
      "splice_source_selected": "dbscSNV1_RF",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.31,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 6.555,
      "phylop100way_prediction": "Uncertain_significance",
      "spliceai_max_score": 0.21,
      "spliceai_max_prediction": "Uncertain_significance",
      "dbscsnv_ada_score": 0.993989770108821,
      "dbscsnv_ada_prediction": "Pathogenic",
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": 3,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PM2,PP3",
      "acmg_by_gene": [
        {
          "score": 3,
          "benign_score": 0,
          "pathogenic_score": 3,
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            "PM2",
            "PP3"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "NM_001081550.2",
          "gene_symbol": "THOC2",
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          "effects": [
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          "inheritance_mode": "XL",
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      ],
      "clinvar_disease": "X-linked intellectual disability-short stature-overweight syndrome",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "X-linked intellectual disability-short stature-overweight syndrome",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}