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The variant's cDNA field may contain extra spaces and wrong prefixes


No checks are done on the content of the cDNA field. The placeholder suggests the format c.1094C>T, however the user is not in any way constrained to follow. Even if the suggestion is followed, the user may introduce leading or trailing spaces (e.g. by copy-pasting from a report). This prevents proper checking for unique variants.

For example, in theory we do not allow the user to enter the same variant twice in a patient record. however, the user may enter c.1094C>T for one variant and c.1094C>T<space> for the next one, overcoming the uniqueness check.




Veronika Koltunova


Sasha Andjic