G35A (p.Gly35Ala) variant of CASR (P41180)
G35A (p.Gly35Ala) in CASR (P41180) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.78 / 1. The record also includes population frequency data, published literature, and structural context.
G35A (p.Gly35Ala) variant details
- p.Gly35Ala
- gnomAD 3-122254293-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.778
- CADD 25.90
- PolyPhen-2 0.87
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available