P41R (p.Pro41Arg) variant of PDE6B (P35913)
P41R (p.Pro41Arg) in PDE6B (P35913) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
P41R (p.Pro41Arg) variant details
- p.Pro41Arg
- rs1231216242
- NCI-TCGA TCGA novel
- ClinGen CA355906209
- ClinVar RCV001307660
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available