S16S (p.Ser16Ser) variant of MYD88 (Q99836)
S16S (p.Ser16Ser) in MYD88 (Q99836) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data, published literature, and structural context.
S16S (p.Ser16Ser) variant details
- p.Ser16Ser
- rs1700988918
- gnomAD 3-38138748-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.188
- AlphaMissense 0.80
- MetaLR 0.13
- MetaSVM -0.91
- CADD 7.54
- PolyPhen-2 1.00
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Structural context available
- Literature evidence available