W18C (p.Trp18Cys) variant of SMAD3 (SMAD family member 3)
W18C (p.Trp18Cys) in SMAD3 (SMAD family member 3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data, published literature, and structural context.
W18C (p.Trp18Cys) variant details
- p.Trp18Cys
- gnomAD 15-67098885-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.0868
- CADD 0.87
- Population evidence available
- Structural context available
- Literature evidence available