R41K (p.Arg41Lys) variant of CSRP3 (P50461)
R41K (p.Arg41Lys) in CSRP3 (P50461) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.49 / 1. The record also includes population frequency data and structural context.
R41K (p.Arg41Lys) variant details
- p.Arg41Lys
- Ensembl rs1850562255
- Missense
- Variant Prioritization Score for Impact Estimate 0.493
- REVEL 0.45
- CADD 19.50
- PolyPhen-2 0.09
- SIFT 0.68
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available