P21S (p.Pro21Ser) variant of MYD88 (Q99836)
P21S (p.Pro21Ser) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.66 / 1. The record also includes population frequency data, published literature, and structural context.
P21S (p.Pro21Ser) variant details
- p.Pro21Ser
- gnomAD 3-38138761-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.661
- CADD 17.10
- PolyPhen-2 0.03
- SIFT 0.14
- Most common in the Non-Finnish European population (allele frequency 9.9e-07)
- Structural context available
- Literature evidence available