P29P (p.Pro29Pro) variant of CNTNAP2 (Q9UHC6)
P29P (p.Pro29Pro) in CNTNAP2 (Q9UHC6) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data, published literature, and structural context.
P29P (p.Pro29Pro) variant details
- p.Pro29Pro
- rs886062049
- gnomAD 7-146116963-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.35
- CADD 12.70
- Most common in the South Asian population (allele frequency 0.00011)
- Structural context available
- Literature evidence available