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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: 5-134606988-C-CGTAA (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=134606988&ref=C&alt=CGTAA&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "5",
      "pos": 134606988,
      "ref": "C",
      "alt": "CGTAA",
      "effect": "frameshift_variant",
      "transcript": "NM_016103.4",
      "consequences": [
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.555_558dupTTAC",
          "hgvs_p": "p.Gly187fs",
          "transcript": "NM_016103.4",
          "protein_id": "NP_057187.1",
          "transcript_support_level": null,
          "aa_start": 186,
          "aa_end": null,
          "aa_length": 198,
          "cds_start": 558,
          "cds_end": null,
          "cds_length": 597,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000402673.7",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_016103.4"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": true,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.555_558dupTTAC",
          "hgvs_p": "p.Gly187fs",
          "transcript": "ENST00000402673.7",
          "protein_id": "ENSP00000385432.2",
          "transcript_support_level": 1,
          "aa_start": 186,
          "aa_end": null,
          "aa_length": 198,
          "cds_start": 558,
          "cds_end": null,
          "cds_length": 597,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_016103.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000402673.7"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.555_558dupTTAC",
          "hgvs_p": "p.Gly187fs",
          "transcript": "ENST00000439578.5",
          "protein_id": "ENSP00000404997.1",
          "transcript_support_level": 1,
          "aa_start": 186,
          "aa_end": null,
          "aa_length": 198,
          "cds_start": 558,
          "cds_end": null,
          "cds_length": 597,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000439578.5"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.351_354dupTTAC",
          "hgvs_p": "p.Gly119fs",
          "transcript": "ENST00000507419.5",
          "protein_id": "ENSP00000425339.1",
          "transcript_support_level": 1,
          "aa_start": 118,
          "aa_end": null,
          "aa_length": 130,
          "cds_start": 354,
          "cds_end": null,
          "cds_length": 393,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000507419.5"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.675_678dupTTAC",
          "hgvs_p": "p.Gly227fs",
          "transcript": "ENST00000950566.1",
          "protein_id": "ENSP00000620625.1",
          "transcript_support_level": null,
          "aa_start": 226,
          "aa_end": null,
          "aa_length": 238,
          "cds_start": 678,
          "cds_end": null,
          "cds_length": 717,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000950566.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.648_651dupTTAC",
          "hgvs_p": "p.Gly218fs",
          "transcript": "ENST00000903497.1",
          "protein_id": "ENSP00000573556.1",
          "transcript_support_level": null,
          "aa_start": 217,
          "aa_end": null,
          "aa_length": 229,
          "cds_start": 651,
          "cds_end": null,
          "cds_length": 690,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000903497.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 9,
          "exon_rank_end": null,
          "exon_count": 9,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.648_651dupTTAC",
          "hgvs_p": "p.Gly218fs",
          "transcript": "ENST00000950567.1",
          "protein_id": "ENSP00000620626.1",
          "transcript_support_level": null,
          "aa_start": 217,
          "aa_end": null,
          "aa_length": 229,
          "cds_start": 651,
          "cds_end": null,
          "cds_length": 690,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000950567.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.555_558dupTTAC",
          "hgvs_p": "p.Gly187fs",
          "transcript": "NM_001033503.3",
          "protein_id": "NP_001028675.1",
          "transcript_support_level": null,
          "aa_start": 186,
          "aa_end": null,
          "aa_length": 198,
          "cds_start": 558,
          "cds_end": null,
          "cds_length": 597,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001033503.3"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.555_558dupTTAC",
          "hgvs_p": "p.Gly187fs",
          "transcript": "ENST00000903489.1",
          "protein_id": "ENSP00000573548.1",
          "transcript_support_level": null,
          "aa_start": 186,
          "aa_end": null,
          "aa_length": 198,
          "cds_start": 558,
          "cds_end": null,
          "cds_length": 597,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000903489.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.555_558dupTTAC",
          "hgvs_p": "p.Gly187fs",
          "transcript": "ENST00000903491.1",
          "protein_id": "ENSP00000573550.1",
          "transcript_support_level": null,
          "aa_start": 186,
          "aa_end": null,
          "aa_length": 198,
          "cds_start": 558,
          "cds_end": null,
          "cds_length": 597,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000903491.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.555_558dupTTAC",
          "hgvs_p": "p.Gly187fs",
          "transcript": "ENST00000903492.1",
          "protein_id": "ENSP00000573551.1",
          "transcript_support_level": null,
          "aa_start": 186,
          "aa_end": null,
          "aa_length": 198,
          "cds_start": 558,
          "cds_end": null,
          "cds_length": 597,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000903492.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.555_558dupTTAC",
          "hgvs_p": "p.Gly187fs",
          "transcript": "ENST00000903493.1",
          "protein_id": "ENSP00000573552.1",
          "transcript_support_level": null,
          "aa_start": 186,
          "aa_end": null,
          "aa_length": 198,
          "cds_start": 558,
          "cds_end": null,
          "cds_length": 597,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000903493.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.555_558dupTTAC",
          "hgvs_p": "p.Gly187fs",
          "transcript": "ENST00000903494.1",
          "protein_id": "ENSP00000573553.1",
          "transcript_support_level": null,
          "aa_start": 186,
          "aa_end": null,
          "aa_length": 198,
          "cds_start": 558,
          "cds_end": null,
          "cds_length": 597,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000903494.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.555_558dupTTAC",
          "hgvs_p": "p.Gly187fs",
          "transcript": "ENST00000903495.1",
          "protein_id": "ENSP00000573554.1",
          "transcript_support_level": null,
          "aa_start": 186,
          "aa_end": null,
          "aa_length": 198,
          "cds_start": 558,
          "cds_end": null,
          "cds_length": 597,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000903495.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.555_558dupTTAC",
          "hgvs_p": "p.Gly187fs",
          "transcript": "ENST00000903496.1",
          "protein_id": "ENSP00000573555.1",
          "transcript_support_level": null,
          "aa_start": 186,
          "aa_end": null,
          "aa_length": 198,
          "cds_start": 558,
          "cds_end": null,
          "cds_length": 597,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000903496.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.555_558dupTTAC",
          "hgvs_p": "p.Gly187fs",
          "transcript": "ENST00000903498.1",
          "protein_id": "ENSP00000573557.1",
          "transcript_support_level": null,
          "aa_start": 186,
          "aa_end": null,
          "aa_length": 198,
          "cds_start": 558,
          "cds_end": null,
          "cds_length": 597,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000903498.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.555_558dupTTAC",
          "hgvs_p": "p.Gly187fs",
          "transcript": "ENST00000903499.1",
          "protein_id": "ENSP00000573558.1",
          "transcript_support_level": null,
          "aa_start": 186,
          "aa_end": null,
          "aa_length": 198,
          "cds_start": 558,
          "cds_end": null,
          "cds_length": 597,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000903499.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.555_558dupTTAC",
          "hgvs_p": "p.Gly187fs",
          "transcript": "ENST00000903500.1",
          "protein_id": "ENSP00000573559.1",
          "transcript_support_level": null,
          "aa_start": 186,
          "aa_end": null,
          "aa_length": 198,
          "cds_start": 558,
          "cds_end": null,
          "cds_length": 597,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000903500.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 8,
          "exon_rank_end": null,
          "exon_count": 8,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.555_558dupTTAC",
          "hgvs_p": "p.Gly187fs",
          "transcript": "ENST00000950564.1",
          "protein_id": "ENSP00000620623.1",
          "transcript_support_level": null,
          "aa_start": 186,
          "aa_end": null,
          "aa_length": 198,
          "cds_start": 558,
          "cds_end": null,
          "cds_length": 597,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000950564.1"
        },
        {
          "aa_ref": "Y",
          "aa_alt": "YL?",
          "canonical": false,
          "protein_coding": true,
          "strand": false,
          "consequences": [
            "frameshift_variant"
          ],
          "exon_rank": 7,
          "exon_rank_end": null,
          "exon_count": 7,
          "intron_rank": null,
          "intron_rank_end": null,
          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "c.555_558dupTTAC",
          "hgvs_p": "p.Gly187fs",
          "transcript": "ENST00000950565.1",
          "protein_id": "ENSP00000620624.1",
          "transcript_support_level": null,
          "aa_start": 186,
          "aa_end": null,
          "aa_length": 198,
          "cds_start": 558,
          "cds_end": null,
          "cds_length": 597,
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        {
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        },
        {
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          "consequences": [
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          ],
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          "exon_count": 7,
          "intron_rank": null,
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          "gene_symbol": "SAR1B",
          "gene_hgnc_id": 10535,
          "hgvs_c": "n.*278_*281dupTTAC",
          "hgvs_p": null,
          "transcript": "ENST00000503318.5",
          "protein_id": "ENSP00000425367.1",
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          "biotype": "nonsense_mediated_decay",
          "feature": "ENST00000503318.5"
        }
      ],
      "gene_symbol": "SAR1B",
      "gene_hgnc_id": 10535,
      "dbsnp": "rs1580645070",
      "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": null,
      "computational_prediction_selected": null,
      "computational_source_selected": null,
      "splice_score_selected": null,
      "splice_prediction_selected": null,
      "splice_source_selected": null,
      "revel_score": null,
      "revel_prediction": null,
      "alphamissense_score": null,
      "alphamissense_prediction": null,
      "bayesdelnoaf_score": null,
      "bayesdelnoaf_prediction": null,
      "phylop100way_score": -0.094,
      "phylop100way_prediction": "Benign",
      "spliceai_max_score": null,
      "spliceai_max_prediction": null,
      "dbscsnv_ada_score": null,
      "dbscsnv_ada_prediction": null,
      "apogee2_score": null,
      "apogee2_prediction": null,
      "mitotip_score": null,
      "mitotip_prediction": null,
      "acmg_score": 5,
      "acmg_classification": "Uncertain_significance",
      "acmg_criteria": "PVS1_Moderate,PM2,PP5",
      "acmg_by_gene": [
        {
          "score": 5,
          "benign_score": 0,
          "pathogenic_score": 5,
          "criteria": [
            "PVS1_Moderate",
            "PM2",
            "PP5"
          ],
          "verdict": "Uncertain_significance",
          "transcript": "NM_016103.4",
          "gene_symbol": "SAR1B",
          "hgnc_id": 10535,
          "effects": [
            "frameshift_variant"
          ],
          "inheritance_mode": "AR",
          "hgvs_c": "c.555_558dupTTAC",
          "hgvs_p": "p.Gly187fs"
        }
      ],
      "clinvar_disease": "Chylomicron retention disease",
      "clinvar_classification": "Pathogenic",
      "clinvar_review_status": "no assertion criteria provided",
      "clinvar_submissions_summary": "null",
      "phenotype_combined": "Chylomicron retention disease",
      "pathogenicity_classification_combined": "Pathogenic",
      "custom_annotations": null
    }
  ],
  "message": null
}