S18C (p.Ser18Cys) variant of MYD88 (Q99836)
S18C (p.Ser18Cys) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data, published literature, and structural context.
S18C (p.Ser18Cys) variant details
- p.Ser18Cys
- gnomAD 3-38138753-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.155
- CADD 13.00
- PolyPhen-2 0.11
- SIFT 0.12
- Most common in the Non-Finnish European population (allele frequency 4.5e-06)
- Structural context available
- Literature evidence available