S19S (p.Ser19Ser) variant of MYD88 (Q99836)
S19S (p.Ser19Ser) in MYD88 (Q99836) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data, published literature, and structural context.
S19S (p.Ser19Ser) variant details
- p.Ser19Ser
- gnomAD 3-38138757-C-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.124
- CADD 6.11
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available