M38I (p.Met38Ile) variant of WAS (P42768)
M38I (p.Met38Ile) in WAS (P42768) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
M38I (p.Met38Ile) variant details
- p.Met38Ile
- ExAC rs782503796
- gnomAD rs782503796
- Missense
- Variant Prioritization Score for Impact Estimate 0.417
- REVEL 0.36
- CADD 22.80
- PolyPhen-2 0.05
- SIFT 0.05
- Most common in the South Asian population (allele frequency 0.00039)
- Structural context available