R38T (p.Arg38Thr) variant of FAS (P25445)
R38T (p.Arg38Thr) in FAS (P25445) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data and structural context.
R38T (p.Arg38Thr) variant details
- p.Arg38Thr
- gnomAD rs1210671749
- Missense
- Variant Prioritization Score for Impact Estimate 0.0971
- CADD 5.38
- PolyPhen-2 0.23
- SIFT 0.10
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available