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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: 19-13206769-G-T (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=13206769&ref=G&alt=T&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "19",
      "pos": 13206769,
      "ref": "G",
      "alt": "T",
      "effect": "non_coding_transcript_exon_variant",
      "transcript": "ENST00000713789.1",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 45,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "n.*2326C>A",
          "hgvs_p": null,
          "transcript": "ENST00000636768.2",
          "protein_id": "ENSP00000490190.2",
          "transcript_support_level": 5,
          "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": 8500,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 47,
          "exon_rank_end": null,
          "exon_count": 47,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "n.*3244C>A",
          "hgvs_p": null,
          "transcript": "ENST00000713789.1",
          "protein_id": "ENSP00000519091.1",
          "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": 8815,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 47,
          "exon_rank_end": null,
          "exon_count": 47,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "c.*544C>A",
          "hgvs_p": null,
          "transcript": "NM_001127222.2",
          "protein_id": "NP_001120694.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2506,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 7521,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8647,
          "mane_select": "ENST00000360228.11",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 47,
          "exon_rank_end": null,
          "exon_count": 47,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "c.*544C>A",
          "hgvs_p": null,
          "transcript": "ENST00000360228.11",
          "protein_id": "ENSP00000353362.5",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2506,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 7521,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8647,
          "mane_select": "NM_001127222.2",
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 47,
          "exon_rank_end": null,
          "exon_count": 47,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "c.*544C>A",
          "hgvs_p": null,
          "transcript": "ENST00000637769.1",
          "protein_id": "ENSP00000489778.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2507,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 7524,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8648,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 46,
          "exon_rank_end": null,
          "exon_count": 46,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "c.*544C>A",
          "hgvs_p": null,
          "transcript": "ENST00000587525.6",
          "protein_id": "ENSP00000467729.2",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2494,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 7485,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8559,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 46,
          "exon_rank_end": null,
          "exon_count": 46,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "c.*544C>A",
          "hgvs_p": null,
          "transcript": "ENST00000637736.1",
          "protein_id": "ENSP00000489861.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2460,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 7383,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8340,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 47,
          "exon_rank_end": null,
          "exon_count": 47,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "c.*1151C>A",
          "hgvs_p": null,
          "transcript": "ENST00000636389.1",
          "protein_id": "ENSP00000489992.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2302,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6909,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8137,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 47,
          "exon_rank_end": null,
          "exon_count": 47,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "c.*1277C>A",
          "hgvs_p": null,
          "transcript": "ENST00000635895.1",
          "protein_id": "ENSP00000490323.1",
          "transcript_support_level": 5,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2261,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6786,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8657,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 47,
          "exon_rank_end": null,
          "exon_count": 47,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "c.*1277C>A",
          "hgvs_p": null,
          "transcript": "ENST00000638009.2",
          "protein_id": "ENSP00000489913.1",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 2261,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6786,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8645,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 45,
          "exon_rank_end": null,
          "exon_count": 45,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "n.*2326C>A",
          "hgvs_p": null,
          "transcript": "ENST00000636768.2",
          "protein_id": "ENSP00000490190.2",
          "transcript_support_level": 5,
          "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": 8500,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 47,
          "exon_rank_end": null,
          "exon_count": 47,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "n.*3244C>A",
          "hgvs_p": null,
          "transcript": "ENST00000713789.1",
          "protein_id": "ENSP00000519091.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
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          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 8815,
          "mane_select": null,
          "mane_plus": null,
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          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 48,
          "exon_rank_end": null,
          "exon_count": 48,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "n.*3149C>A",
          "hgvs_p": null,
          "transcript": "ENST00000573891.7",
          "protein_id": "ENSP00000460276.2",
          "transcript_support_level": 5,
          "aa_start": null,
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          "cdna_start": null,
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          "cdna_length": 8730,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 48,
          "exon_rank_end": null,
          "exon_count": 48,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "n.*7737C>A",
          "hgvs_p": null,
          "transcript": "ENST00000574974.4",
          "protein_id": "ENSP00000459963.3",
          "transcript_support_level": 5,
          "aa_start": null,
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          "cds_start": -4,
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          "cds_length": null,
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          "cdna_length": 8493,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 49,
          "exon_rank_end": null,
          "exon_count": 49,
          "intron_rank": null,
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          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "n.*3246C>A",
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          "transcript": "ENST00000636058.2",
          "protein_id": "ENSP00000490075.2",
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          "biotype": null,
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 48,
          "exon_rank_end": null,
          "exon_count": 48,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "n.*3180C>A",
          "hgvs_p": null,
          "transcript": "ENST00000637777.2",
          "protein_id": "ENSP00000490475.2",
          "transcript_support_level": 5,
          "aa_start": null,
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          "cds_length": null,
          "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": false,
          "strand": false,
          "consequences": [
            "non_coding_transcript_exon_variant"
          ],
          "exon_rank": 47,
          "exon_rank_end": null,
          "exon_count": 47,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "n.*7481C>A",
          "hgvs_p": null,
          "transcript": "ENST00000713788.1",
          "protein_id": "ENSP00000519090.1",
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          "cdna_length": 8606,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 48,
          "exon_rank_end": null,
          "exon_count": 48,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "c.*544C>A",
          "hgvs_p": null,
          "transcript": "NM_023035.3",
          "protein_id": "NP_075461.2",
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          "feature": null
        },
        {
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          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 48,
          "exon_rank_end": null,
          "exon_count": 48,
          "intron_rank": null,
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          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "c.*544C>A",
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          "transcript": "ENST00000637819.2",
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          "mane_select": null,
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          "feature": null
        },
        {
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          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 48,
          "exon_rank_end": null,
          "exon_count": 48,
          "intron_rank": null,
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          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "c.*1277C>A",
          "hgvs_p": null,
          "transcript": "NM_000068.4",
          "protein_id": "NP_000059.3",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 2266,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": 6801,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": 8660,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 48,
          "exon_rank_end": null,
          "exon_count": 48,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "c.*1277C>A",
          "hgvs_p": null,
          "transcript": "NM_001174080.2",
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        },
        {
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          "protein_coding": true,
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          "intron_rank": null,
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          "gene_symbol": "CACNA1A",
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          "intron_rank": null,
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          "gene_symbol": "CACNA1A",
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          "hgvs_c": "n.*7737C>A",
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          "transcript": "ENST00000574974.4",
          "protein_id": "ENSP00000459963.3",
          "transcript_support_level": 5,
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          "exon_count": 49,
          "intron_rank": null,
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          "cdna_length": 8823,
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          "feature": null
        },
        {
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          "protein_coding": false,
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          ],
          "exon_rank": 48,
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          "exon_count": 48,
          "intron_rank": null,
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          "gene_symbol": "CACNA1A",
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          "hgvs_c": "n.*3180C>A",
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          "transcript": "ENST00000637777.2",
          "protein_id": "ENSP00000490475.2",
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          "cdna_length": 8757,
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          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "3_prime_UTR_variant"
          ],
          "exon_rank": 47,
          "exon_rank_end": null,
          "exon_count": 47,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "CACNA1A",
          "gene_hgnc_id": 1388,
          "hgvs_c": "n.*7481C>A",
          "hgvs_p": null,
          "transcript": "ENST00000713788.1",
          "protein_id": "ENSP00000519090.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": -4,
          "cds_end": null,
          "cds_length": null,
          "cdna_start": null,
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          "cdna_length": 8606,
          "mane_select": null,
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          "biotype": null,
          "feature": null
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "ENSG00000300728",
          "gene_hgnc_id": null,
          "hgvs_c": "n.413+1346G>T",
          "hgvs_p": null,
          "transcript": "ENST00000773684.1",
          "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,
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          "cdna_length": 686,
          "mane_select": null,
          "mane_plus": null,
          "biotype": null,
          "feature": null
        }
      ],
      "gene_symbol": "CACNA1A",
      "gene_hgnc_id": 1388,
      "dbsnp": "rs141221917",
      "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": -0.5400000214576721,
      "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": -0.54,
      "bayesdelnoaf_prediction": "Benign",
      "phylop100way_score": 3.375,
      "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": -2,
      "acmg_classification": "Likely_benign",
      "acmg_criteria": "PM2,BP4_Strong",
      "acmg_by_gene": [
        {
          "score": -2,
          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000713789.1",
          "gene_symbol": "CACNA1A",
          "hgnc_id": 1388,
          "effects": [
            "non_coding_transcript_exon_variant"
          ],
          "inheritance_mode": "AD",
          "hgvs_c": "n.*3244C>A",
          "hgvs_p": null
        },
        {
          "score": -2,
          "benign_score": 4,
          "pathogenic_score": 2,
          "criteria": [
            "PM2",
            "BP4_Strong"
          ],
          "verdict": "Likely_benign",
          "transcript": "ENST00000773684.1",
          "gene_symbol": "ENSG00000300728",
          "hgnc_id": null,
          "effects": [
            "intron_variant"
          ],
          "inheritance_mode": "",
          "hgvs_c": "n.413+1346G>T",
          "hgvs_p": null
        }
      ],
      "clinvar_disease": "not specified",
      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "not specified",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
    }
  ],
  "message": null
}