P39P (p.Pro39Pro) variant of CASR (P41180)
P39P (p.Pro39Pro) in CASR (P41180) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data, published literature, and structural context.
P39P (p.Pro39Pro) variant details
- p.Pro39Pro
- rs1316125812
- gnomAD 3-122254306-T-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.225
- CADD 10.90
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available
- Literature evidence available