P13L (p.Pro13Leu) variant of MYD88 (Q99836)
P13L (p.Pro13Leu) in MYD88 (Q99836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.07 / 1. The record also includes population frequency data, published literature, and structural context.
P13L (p.Pro13Leu) variant details
- p.Pro13Leu
- gnomAD 3-38138738-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.0687
- CADD 1.25
- PolyPhen-2 0.00
- SIFT 0.38
- Population evidence available
- Structural context available
- Literature evidence available