V17V (p.Val17Val) variant of CSRP3 (P50461)
V17V (p.Val17Val) in CSRP3 (P50461) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data, published literature, and structural context.
V17V (p.Val17Val) variant details
- p.Val17Val
- gnomAD 11-19192398-G-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.514
- CADD 7.35
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available