R41Q (p.Arg41Gln) variant of CSRP3 (P50461)
R41Q (p.Arg41Gln) in CSRP3 (P50461) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.07 / 1. The record also includes population frequency data, published literature, and structural context.
R41Q (p.Arg41Gln) variant details
- p.Arg41Gln
- rs142832902
- gnomAD 11-19186336-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.0677
- CADD 0.59
- SIFT 0.56
- Population evidence available
- Structural context available
- Literature evidence available