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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: 2-239082174-G-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=239082174&ref=G&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "2",
      "pos": 239082174,
      "ref": "G",
      "alt": "T",
      "effect": "synonymous_variant",
      "transcript": "NM_001378414.1",
      "consequences": [
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2580C>A",
          "hgvs_p": "p.Pro860Pro",
          "transcript": "NM_001378414.1",
          "protein_id": "NP_001365343.1",
          "transcript_support_level": null,
          "aa_start": 860,
          "aa_end": null,
          "aa_length": 1089,
          "cds_start": 2580,
          "cds_end": null,
          "cds_length": 3270,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000543185.6",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001378414.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2580C>A",
          "hgvs_p": "p.Pro860Pro",
          "transcript": "ENST00000543185.6",
          "protein_id": "ENSP00000440481.3",
          "transcript_support_level": 5,
          "aa_start": 860,
          "aa_end": null,
          "aa_length": 1089,
          "cds_start": 2580,
          "cds_end": null,
          "cds_length": 3270,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_001378414.1",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000543185.6"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2565C>A",
          "hgvs_p": "p.Pro855Pro",
          "transcript": "ENST00000345617.7",
          "protein_id": "ENSP00000264606.3",
          "transcript_support_level": 1,
          "aa_start": 855,
          "aa_end": null,
          "aa_length": 1084,
          "cds_start": 2565,
          "cds_end": null,
          "cds_length": 3255,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000345617.7"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2580C>A",
          "hgvs_p": "p.Pro860Pro",
          "transcript": "NM_001378415.1",
          "protein_id": "NP_001365344.1",
          "transcript_support_level": null,
          "aa_start": 860,
          "aa_end": null,
          "aa_length": 1089,
          "cds_start": 2580,
          "cds_end": null,
          "cds_length": 3270,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001378415.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2580C>A",
          "hgvs_p": "p.Pro860Pro",
          "transcript": "ENST00000896768.1",
          "protein_id": "ENSP00000566827.1",
          "transcript_support_level": null,
          "aa_start": 860,
          "aa_end": null,
          "aa_length": 1089,
          "cds_start": 2580,
          "cds_end": null,
          "cds_length": 3270,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000896768.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2580C>A",
          "hgvs_p": "p.Pro860Pro",
          "transcript": "ENST00000913664.1",
          "protein_id": "ENSP00000583723.1",
          "transcript_support_level": null,
          "aa_start": 860,
          "aa_end": null,
          "aa_length": 1089,
          "cds_start": 2580,
          "cds_end": null,
          "cds_length": 3270,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000913664.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2580C>A",
          "hgvs_p": "p.Pro860Pro",
          "transcript": "ENST00000913672.1",
          "protein_id": "ENSP00000583731.1",
          "transcript_support_level": null,
          "aa_start": 860,
          "aa_end": null,
          "aa_length": 1089,
          "cds_start": 2580,
          "cds_end": null,
          "cds_length": 3270,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000913672.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2574C>A",
          "hgvs_p": "p.Pro858Pro",
          "transcript": "ENST00000913671.1",
          "protein_id": "ENSP00000583730.1",
          "transcript_support_level": null,
          "aa_start": 858,
          "aa_end": null,
          "aa_length": 1087,
          "cds_start": 2574,
          "cds_end": null,
          "cds_length": 3264,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000913671.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2574C>A",
          "hgvs_p": "p.Pro858Pro",
          "transcript": "ENST00000971555.1",
          "protein_id": "ENSP00000641614.1",
          "transcript_support_level": null,
          "aa_start": 858,
          "aa_end": null,
          "aa_length": 1087,
          "cds_start": 2574,
          "cds_end": null,
          "cds_length": 3264,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000971555.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2565C>A",
          "hgvs_p": "p.Pro855Pro",
          "transcript": "NM_001378416.1",
          "protein_id": "NP_001365345.1",
          "transcript_support_level": null,
          "aa_start": 855,
          "aa_end": null,
          "aa_length": 1084,
          "cds_start": 2565,
          "cds_end": null,
          "cds_length": 3255,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001378416.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2565C>A",
          "hgvs_p": "p.Pro855Pro",
          "transcript": "NM_001378417.1",
          "protein_id": "NP_001365346.1",
          "transcript_support_level": null,
          "aa_start": 855,
          "aa_end": null,
          "aa_length": 1084,
          "cds_start": 2565,
          "cds_end": null,
          "cds_length": 3255,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001378417.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2565C>A",
          "hgvs_p": "p.Pro855Pro",
          "transcript": "NM_006037.4",
          "protein_id": "NP_006028.2",
          "transcript_support_level": null,
          "aa_start": 855,
          "aa_end": null,
          "aa_length": 1084,
          "cds_start": 2565,
          "cds_end": null,
          "cds_length": 3255,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_006037.4"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2565C>A",
          "hgvs_p": "p.Pro855Pro",
          "transcript": "ENST00000896770.1",
          "protein_id": "ENSP00000566829.1",
          "transcript_support_level": null,
          "aa_start": 855,
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          "aa_length": 1084,
          "cds_start": 2565,
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          "cds_length": 3255,
          "cdna_start": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000896770.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2565C>A",
          "hgvs_p": "p.Pro855Pro",
          "transcript": "ENST00000896771.1",
          "protein_id": "ENSP00000566830.1",
          "transcript_support_level": null,
          "aa_start": 855,
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          "cds_start": 2565,
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        },
        {
          "aa_ref": "P",
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          "protein_coding": true,
          "strand": false,
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          "exon_count": 27,
          "intron_rank": null,
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          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2565C>A",
          "hgvs_p": "p.Pro855Pro",
          "transcript": "ENST00000913662.1",
          "protein_id": "ENSP00000583721.1",
          "transcript_support_level": null,
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          "cds_start": 2565,
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          "biotype": "protein_coding",
          "feature": "ENST00000913662.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2565C>A",
          "hgvs_p": "p.Pro855Pro",
          "transcript": "ENST00000913665.1",
          "protein_id": "ENSP00000583724.1",
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          "biotype": "protein_coding",
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        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": 21,
          "exon_rank_end": null,
          "exon_count": 27,
          "intron_rank": null,
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          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2565C>A",
          "hgvs_p": "p.Pro855Pro",
          "transcript": "ENST00000913673.1",
          "protein_id": "ENSP00000583732.1",
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        {
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          ],
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          "hgvs_c": "c.2550C>A",
          "hgvs_p": "p.Pro850Pro",
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        {
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          ],
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          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2502C>A",
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          "transcript": "ENST00000913667.1",
          "protein_id": "ENSP00000583726.1",
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          "biotype": "protein_coding",
          "feature": "ENST00000913667.1"
        },
        {
          "aa_ref": "P",
          "aa_alt": "P",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "synonymous_variant"
          ],
          "exon_rank": 20,
          "exon_rank_end": null,
          "exon_count": 26,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2499C>A",
          "hgvs_p": "p.Pro833Pro",
          "transcript": "NM_001435991.1",
          "protein_id": "NP_001422920.1",
          "transcript_support_level": null,
          "aa_start": 833,
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          "aa_length": 1062,
          "cds_start": 2499,
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          "cds_length": 3189,
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          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "c.2361C>A",
          "hgvs_p": "p.Pro787Pro",
          "transcript": "XM_047446498.1",
          "protein_id": "XP_047302454.1",
          "transcript_support_level": null,
          "aa_start": 787,
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          "aa_length": 1016,
          "cds_start": 2361,
          "cds_end": null,
          "cds_length": 3051,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "XM_047446498.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "n.472C>A",
          "hgvs_p": null,
          "transcript": "ENST00000487617.5",
          "protein_id": null,
          "transcript_support_level": 3,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "retained_intron",
          "feature": "ENST00000487617.5"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 4,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "HDAC4",
          "gene_hgnc_id": 14063,
          "hgvs_c": "n.594C>A",
          "hgvs_p": null,
          "transcript": "ENST00000690129.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": null,
          "cds_start": null,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "retained_intron",
          "feature": "ENST00000690129.1"
        }
      ],
      "gene_symbol": "HDAC4",
      "gene_hgnc_id": 14063,
      "dbsnp": "rs1063639",
      "frequency_reference_population": null,
      "hom_count_reference_population": 0,
      "allele_count_reference_population": 0,
      "gnomad_exomes_af": 0,
      "gnomad_genomes_af": null,
      "gnomad_exomes_ac": 0,
      "gnomad_genomes_ac": null,
      "gnomad_exomes_homalt": 0,
      "gnomad_genomes_homalt": null,
      "gnomad_mito_homoplasmic": null,
      "gnomad_mito_heteroplasmic": null,
      "computational_score_selected": -0.8100000023841858,
      "computational_prediction_selected": "Benign",
      "computational_source_selected": "BayesDel_noAF",
      "splice_score_selected": 0,
      "splice_prediction_selected": "Benign",
      "splice_source_selected": "max_spliceai",
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": -0.81,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 0.073,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": 0,
      "spliceai_max_prediction": "Benign",
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": -3,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong,BP7",
      "acmg_by_gene": [
        {
          "score": -3,
          "benign_score": 5,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong",
            "BP7"
          ],
          "verdict": "Likely_benign",
          "transcript": "NM_001378414.1",
          "gene_symbol": "HDAC4",
          "hgnc_id": 14063,
          "effects": [
            "synonymous_variant"
          ],
          "inheritance_mode": "AD,Unknown",
          "hgvs_c": "c.2580C>A",
          "hgvs_p": "p.Pro860Pro"
        }
      ],
      "clinvar_disease": "",
      "clinvar_classification": "",
      "clinvar_review_status": "",
      "clinvar_submissions_summary": "",
      "phenotype_combined": null,
      "pathogenicity_classification_combined": null,
      "custom_annotations": null
    }
  ],
  "message": null
}