F38F (p.Phe38Phe) variant of CASR (P41180)
F38F (p.Phe38Phe) in CASR (P41180) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data, published literature, and structural context.
F38F (p.Phe38Phe) variant details
- p.Phe38Phe
- rs61733590
- gnomAD 3-122254303-T-C
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.453
- CADD 11.30
- Most common in the Middle Eastern population (allele frequency 0.00017)
- Structural context available
- Literature evidence available