G19W (p.Gly19Trp) variant of MCCC2 (Q9HCC0)
G19W (p.Gly19Trp) in MCCC2 (Q9HCC0) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data, published literature, and structural context.
G19W (p.Gly19Trp) variant details
- p.Gly19Trp
- gnomAD 5-71587480-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.312
- REVEL 0.43
- CADD 11.10
- PolyPhen-2 0.35
- SIFT 0.18
- Population evidence available
- Structural context available
- Literature evidence available