G17W (p.Gly17Trp) variant of SMAD3 (SMAD family member 3)
G17W (p.Gly17Trp) in SMAD3 (SMAD family member 3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data, published literature, and structural context.
G17W (p.Gly17Trp) variant details
- p.Gly17Trp
- gnomAD 15-67098880-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.107
- CADD 3.78
- Population evidence available
- Structural context available
- Literature evidence available