F8F (p.Phe8Phe) variant of MAPT (P10636)
F8F (p.Phe8Phe) in MAPT (P10636) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.10 / 1. The record also includes population frequency data, published literature, and structural context.
F8F (p.Phe8Phe) variant details
- p.Phe8Phe
- rs886700939
- gnomAD 17-45962361-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.101
- CADD 2.91
- Most common in the Non-Finnish European population (allele frequency 9.9e-07)
- Structural context available
- Literature evidence available