P42Q (p.Pro42Gln) variant of PDE6B (P35913)
P42Q (p.Pro42Gln) in PDE6B (P35913) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P42Q (p.Pro42Gln) variant details
- p.Pro42Gln
- NCI-TCGA Cosmic COSV5533
- cosmic curated COSV55330
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available