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Database Description File
UNC13D Variants of UNC13D gene of FHL syndrome found in the literature

REST API

Database of UNC13D variants


    import requests
    r = requests.get('https://www.biotoclin.org/predictor/FHLdb/api/UNC13D/')
    r.json()
          

    curl  --request GET --url 'https://www.biotoclin.org/predictor/FHLdb/api/UNC13D/'
    

    wget -q 'https://www.biotoclin.org/predictor/FHLdb/api/UNC13D/' -O -

Annotation of a single variant


    import requests
    r = requests.get('https://www.biotoclin.org/predictor/FHLdb/api/UNC13D/<variant>/')
    r.json()
        

    curl  --request GET --url 'https://www.biotoclin.org/predictor/FHLdb/api/UNC13D/<variant>/'
    

    wget -q 'https://www.biotoclin.org/predictor/FHLdb/api/UNC13D/<variant>/' -O -

The parameter:

  • variant: transcript or protein variant in HGVS nomenclature such as c.32G>C or p.Arg11Pro

License

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FHLdb data is licensed under a
Creative Commons Attribution-ShareAlike 4.0 International License

Disclaimer This resource is uniquely intended for research purposes. The authors are not responsible for neither its use nor misuse. The data provided are not intended as advice of any kind. The authors have worked with care in the development of this server, but assume no liability or responsibility for any error, weakness, incompleteness or temporariness of the resource and of the data provided.