S39S (p.Ser39Ser) variant of SMARCA2 (P51531)
S39S (p.Ser39Ser) in SMARCA2 (P51531) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data, published literature, and structural context.
S39S (p.Ser39Ser) variant details
- p.Ser39Ser
- rs760818868
- gnomAD 9-2029139-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.135
- CADD 7.64
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00038)
- Structural context available
- Literature evidence available