P69P (p.Pro69Pro) variant of CDC42 (P60953)
P69P (p.Pro69Pro) in CDC42 (P60953) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.49 / 1. The record also includes population frequency data, published literature, and structural context.
P69P (p.Pro69Pro) variant details
- p.Pro69Pro
- rs368234616
- gnomAD 1-22086467-G-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.494
- CADD 11.60
- Most common in the East Asian population (allele frequency 0.00015)
- Structural context available
- Literature evidence available