S41S (p.Ser41Ser) variant of CNTNAP2 (Q9UHC6)
S41S (p.Ser41Ser) in CNTNAP2 (Q9UHC6) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
S41S (p.Ser41Ser) variant details
- p.Ser41Ser
- gnomAD 7-146774296-T-A
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.0944
- CADD 1.94
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available