R13R (p.Arg13Arg) variant of WAS (P42768)
R13R (p.Arg13Arg) in WAS (P42768) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
R13R (p.Arg13Arg) variant details
- p.Arg13Arg
- rs2062410511
- gnomAD X-48683892-A-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0931
- CADD 1.76
- Most common in the REMAINING population (allele frequency 6.5e-05)
- Structural context available
- Literature evidence available