S5G (p.Ser5Gly) variant of CASR (P41180)
S5G (p.Ser5Gly) in CASR (P41180) 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.
S5G (p.Ser5Gly) variant details
- p.Ser5Gly
- gnomAD rs2074527950
- Missense
- Variant Prioritization Score for Impact Estimate 0.0966
- CADD 3.83
- PolyPhen-2 0.00
- SIFT 0.63
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available