10 likes | 126 Views
This report examines the genetic variant .c.160C>T (p.Arg54*) within the WWOX gene located in exon 2. The nonsense mutation results in a premature stop codon, potentially leading to a significant loss of function in the WWOX protein. This variant may be implicated in various pathologies based on the role of WWOX in cellular processes and tumor suppression. Further functional studies and clinical correlation are recommended to elucidate its impact on health.
E N D