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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: 12-79079879-G-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=79079879&ref=G&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "12",
      "pos": 79079879,
      "ref": "G",
      "alt": "T",
      "effect": "intron_variant",
      "transcript": "ENST00000261205.9",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-18+32517G>T",
          "hgvs_p": null,
          "transcript": "NM_005639.3",
          "protein_id": "NP_005630.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 422,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1269,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4705,
          "mane_select": "ENST00000261205.9",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 11,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-18+32517G>T",
          "hgvs_p": null,
          "transcript": "ENST00000261205.9",
          "protein_id": "ENSP00000261205.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 422,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1269,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4705,
          "mane_select": "NM_005639.3",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-18+32517G>T",
          "hgvs_p": null,
          "transcript": "ENST00000393240.7",
          "protein_id": "ENSP00000376932.3",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 422,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1269,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 3095,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-18+32517G>T",
          "hgvs_p": null,
          "transcript": "ENST00000552744.5",
          "protein_id": "ENSP00000447575.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 422,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1269,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2718,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-18+101948G>T",
          "hgvs_p": null,
          "transcript": "ENST00000457153.6",
          "protein_id": "ENSP00000391056.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 419,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1260,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4592,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-18+32517G>T",
          "hgvs_p": null,
          "transcript": "ENST00000549671.5",
          "protein_id": "ENSP00000450321.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 71,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 217,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 710,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 1,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LOC105369863",
          "gene_hgnc_id": null,
          "hgvs_c": "n.23001C>A",
          "hgvs_p": null,
          "transcript": "XR_007063384.1",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 34276,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 3,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "LOC105369863",
          "gene_hgnc_id": null,
          "hgvs_c": "n.19570C>A",
          "hgvs_p": null,
          "transcript": "XR_007063385.1",
          "protein_id": null,
          "transcript_support_level": null,
          "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": 30845,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-18+32517G>T",
          "hgvs_p": null,
          "transcript": "NM_001135805.2",
          "protein_id": "NP_001129277.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 422,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1269,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4835,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-18+32517G>T",
          "hgvs_p": null,
          "transcript": "NM_001135806.2",
          "protein_id": "NP_001129278.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 422,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1269,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4371,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 10,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-18+101948G>T",
          "hgvs_p": null,
          "transcript": "NM_001415938.1",
          "protein_id": "NP_001402867.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 422,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1269,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4639,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-59-23135G>T",
          "hgvs_p": null,
          "transcript": "NM_001415939.1",
          "protein_id": "NP_001402868.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 422,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1269,
          "cdna_start": null,
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          "cdna_length": 4747,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-18+32517G>T",
          "hgvs_p": null,
          "transcript": "NM_001415940.1",
          "protein_id": "NP_001402869.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 422,
          "cds_start": -4,
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          "cds_length": 1269,
          "cdna_start": null,
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          "cdna_length": 4794,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-18+32517G>T",
          "hgvs_p": null,
          "transcript": "ENST00000704696.1",
          "protein_id": "ENSP00000515993.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 422,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 1269,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 4842,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-18+32517G>T",
          "hgvs_p": null,
          "transcript": "ENST00000704700.1",
          "protein_id": "ENSP00000515997.1",
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          "cdna_start": null,
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          "mane_select": null,
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          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 12,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-18+32517G>T",
          "hgvs_p": null,
          "transcript": "ENST00000704702.1",
          "protein_id": "ENSP00000515999.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 422,
          "cds_start": -4,
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          "cds_length": 1269,
          "cdna_start": null,
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          "cdna_length": 4720,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-93+32517G>T",
          "hgvs_p": null,
          "transcript": "ENST00000704704.1",
          "protein_id": "ENSP00000516001.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 422,
          "cds_start": -4,
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          "cds_length": 1269,
          "cdna_start": null,
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          "cdna_length": 4773,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 13,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-18+32517G>T",
          "hgvs_p": null,
          "transcript": "ENST00000704705.1",
          "protein_id": "ENSP00000516002.1",
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          "cdna_start": null,
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          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 13,
          "intron_rank": 5,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-18+32517G>T",
          "hgvs_p": null,
          "transcript": "ENST00000704706.1",
          "protein_id": "ENSP00000516003.1",
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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": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 11,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-18+32517G>T",
          "hgvs_p": null,
          "transcript": "ENST00000704708.1",
          "protein_id": "ENSP00000516005.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 422,
          "cds_start": -4,
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          "cds_length": 1269,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 2733,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 12,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "SYT1",
          "gene_hgnc_id": 11509,
          "hgvs_c": "c.-212+32517G>T",
          "hgvs_p": null,
          "transcript": "ENST00000704710.1",
          "protein_id": "ENSP00000516007.1",
          "transcript_support_level": null,
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          "aa_end": null,
          "aa_length": 422,
          "cds_start": -4,
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      "acmg_classification": "Benign",
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      "acmg_by_gene": [
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          "verdict": "Benign",
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          "verdict": "Benign",
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          "gene_symbol": "LOC105369863",
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          "effects": [
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          "inheritance_mode": "",
          "hgvs_c": "n.23001C>A",
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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
}