P38P (p.Pro38Pro) variant of CNTNAP2 (Q9UHC6)
P38P (p.Pro38Pro) in CNTNAP2 (Q9UHC6) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data, published literature, and structural context.
P38P (p.Pro38Pro) variant details
- p.Pro38Pro
- rs778648331
- gnomAD 7-146774287-A-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0814
- CADD 0.10
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available