The gene encoding what is now known as Serine Threonine Kinase 19 (STK19) provides a further illustrative example of such misinterpretation.2 Indeed, the identified melanoma driver mutation STK19 D89N3 turned out not to be in the coding region of the expressed form of STK19, which in reality lacks the first 110 amino acids shown in database annotations. Here, WHR1 is linked to melanoma.