W38L (p.Trp38Leu) variant of C2CD2L (O14523)
W38L (p.Trp38Leu) in C2CD2L (O14523) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data, published literature, and structural context.
W38L (p.Trp38Leu) variant details
- p.Trp38Leu
- gnomAD 11-119107854-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.297
- REVEL 0.06
- ESM-1b 0.00
- AlphaMissense 0.17
- CADD 23.30
- PolyPhen-2 0.01
- SIFT 0.14
- Population evidence available
- Structural context available
- Literature evidence available