F22F (p.Phe22Phe) variant of MSH2 (DNA mismatch repair protein Msh2)
F22F (p.Phe22Phe) in MSH2 (DNA mismatch repair protein Msh2) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data, published literature, and structural context.
F22F (p.Phe22Phe) variant details
- p.Phe22Phe
- rs200632093
- gnomAD 2-47403257-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.32
- CADD 15.90
- Most common in the HGDP:CAMBODIAN population (allele frequency 0.1)
- Structural context available
- Literature evidence available