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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: 5-137870126-T-TA (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=137870126&ref=T&alt=TA&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "5",
      "pos": 137870126,
      "ref": "T",
      "alt": "TA",
      "effect": "intron_variant",
      "transcript": "NM_006790.3",
      "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": 10,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "MYOT",
          "gene_hgnc_id": 12399,
          "hgvs_c": "c.-211-297dupA",
          "hgvs_p": null,
          "transcript": "NM_006790.3",
          "protein_id": "NP_006781.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 498,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1497,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000239926.9",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_006790.3"
        },
        {
          "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": 10,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "MYOT",
          "gene_hgnc_id": 12399,
          "hgvs_c": "c.-211-315_-211-314insA",
          "hgvs_p": null,
          "transcript": "ENST00000239926.9",
          "protein_id": "ENSP00000239926.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 498,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1497,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_006790.3",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000239926.9"
        },
        {
          "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "MYOT",
          "gene_hgnc_id": 12399,
          "hgvs_c": "c.-211-315_-211-314insA",
          "hgvs_p": null,
          "transcript": "ENST00000968642.1",
          "protein_id": "ENSP00000638701.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 497,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1494,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000968642.1"
        },
        {
          "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "MYOT",
          "gene_hgnc_id": 12399,
          "hgvs_c": "c.-205-297dupA",
          "hgvs_p": null,
          "transcript": "NM_001300911.2",
          "protein_id": "NP_001287840.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 383,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1152,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001300911.2"
        },
        {
          "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "MYOT",
          "gene_hgnc_id": 12399,
          "hgvs_c": "c.-205-315_-205-314insA",
          "hgvs_p": null,
          "transcript": "ENST00000515645.1",
          "protein_id": "ENSP00000426281.1",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 383,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 1152,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000515645.1"
        },
        {
          "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "MYOT",
          "gene_hgnc_id": 12399,
          "hgvs_c": "c.-281-297dupA",
          "hgvs_p": null,
          "transcript": "NM_001135940.2",
          "protein_id": "NP_001129412.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 314,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 945,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001135940.2"
        },
        {
          "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": 1,
          "intron_rank_end": null,
          "gene_symbol": "MYOT",
          "gene_hgnc_id": 12399,
          "hgvs_c": "c.-281-315_-281-314insA",
          "hgvs_p": null,
          "transcript": "ENST00000421631.6",
          "protein_id": "ENSP00000391185.2",
          "transcript_support_level": 2,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 314,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 945,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000421631.6"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 6,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "MYOT",
          "gene_hgnc_id": 12399,
          "hgvs_c": "n.95-315_95-314insA",
          "hgvs_p": null,
          "transcript": "ENST00000509812.5",
          "protein_id": null,
          "transcript_support_level": 3,
          "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": "pseudogene",
          "feature": "ENST00000509812.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": true,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 3,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "MYOT",
          "gene_hgnc_id": 12399,
          "hgvs_c": "n.95-315_95-314insA",
          "hgvs_p": null,
          "transcript": "ENST00000511625.5",
          "protein_id": null,
          "transcript_support_level": 3,
          "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": "ENST00000511625.5"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PKD2L2-DT",
          "gene_hgnc_id": 55557,
          "hgvs_c": "n.371-10864_371-10863insT",
          "hgvs_p": null,
          "transcript": "ENST00000514616.7",
          "protein_id": null,
          "transcript_support_level": 5,
          "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": "pseudogene",
          "feature": "ENST00000514616.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 4,
          "intron_rank": 1,
          "intron_rank_end": null,
          "gene_symbol": "PKD2L2-DT",
          "gene_hgnc_id": 55557,
          "hgvs_c": "n.147+10181_147+10182insT",
          "hgvs_p": null,
          "transcript": "ENST00000661977.1",
          "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": "pseudogene",
          "feature": "ENST00000661977.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
          "exon_rank": null,
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          "exon_count": 5,
          "intron_rank": 1,
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          "gene_symbol": "PKD2L2-DT",
          "gene_hgnc_id": 55557,
          "hgvs_c": "n.87+10181_87+10182insT",
          "hgvs_p": null,
          "transcript": "ENST00000666934.1",
          "protein_id": null,
          "transcript_support_level": null,
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          "cds_start": null,
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          "cds_length": null,
          "cdna_start": null,
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          "mane_select": null,
          "mane_plus": null,
          "biotype": "pseudogene",
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        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
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          ],
          "exon_rank": null,
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          "gene_symbol": "PKD2L2-DT",
          "gene_hgnc_id": 55557,
          "hgvs_c": "n.318-10864_318-10863insT",
          "hgvs_p": null,
          "transcript": "ENST00000728404.1",
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          "cds_start": null,
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
            "intron_variant"
          ],
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          "exon_count": 6,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PKD2L2-DT",
          "gene_hgnc_id": 55557,
          "hgvs_c": "n.302-10864_302-10863insT",
          "hgvs_p": null,
          "transcript": "ENST00000728405.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": null,
          "cds_start": null,
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          "cdna_start": null,
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        },
        {
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          "gene_symbol": "PKD2L2-DT",
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        },
        {
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          "canonical": false,
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          "consequences": [
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          ],
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          "gene_symbol": "PKD2L2-DT",
          "gene_hgnc_id": 55557,
          "hgvs_c": "n.362-10864_362-10863insT",
          "hgvs_p": null,
          "transcript": "ENST00000728407.1",
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          "feature": "ENST00000728407.1"
        },
        {
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          "canonical": false,
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          "strand": false,
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          ],
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          "exon_count": 6,
          "intron_rank": 2,
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          "gene_symbol": "PKD2L2-DT",
          "gene_hgnc_id": 55557,
          "hgvs_c": "n.303-10864_303-10863insT",
          "hgvs_p": null,
          "transcript": "ENST00000728408.1",
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          "biotype": "pseudogene",
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        },
        {
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          "consequences": [
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          ],
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          "intron_rank": 1,
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          "gene_symbol": "PKD2L2-DT",
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          "hgvs_c": "n.189-10864_189-10863insT",
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        },
        {
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          "protein_coding": false,
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          "gene_symbol": "PKD2L2-DT",
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          "hgvs_c": "n.187-10864_187-10863insT",
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        },
        {
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          "consequences": [
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          ],
          "exon_rank": null,
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          "exon_count": 7,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "PKD2L2-DT",
          "gene_hgnc_id": 55557,
          "hgvs_c": "n.357-10864_357-10863insT",
          "hgvs_p": null,
          "transcript": "ENST00000728411.1",
          "protein_id": null,
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
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          "cds_start": null,
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          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "pseudogene",
          "feature": "ENST00000728411.1"
        },
        {
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          "canonical": false,
          "protein_coding": false,
          "strand": false,
          "consequences": [
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          ],
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          "exon_rank_end": null,
          "exon_count": 5,
          "intron_rank": 2,
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      "clinvar_classification": "Likely benign",
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      "phenotype_combined": "not provided",
      "pathogenicity_classification_combined": "Likely benign",
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  "message": null
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