M38R (p.Met38Arg) variant of WAS (P42768)
M38R (p.Met38Arg) in WAS (P42768) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.62 / 1. The record also includes population frequency data and structural context.
M38R (p.Met38Arg) variant details
- p.Met38Arg
- ExAC rs781839950
- gnomAD rs781839950
- Missense
- Variant Prioritization Score for Impact Estimate 0.621
- REVEL 0.66
- CADD 26.40
- PolyPhen-2 0.74
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available