G13W (p.Gly13Trp) variant of LAMA3 (Laminin subunit alpha-3)
G13W (p.Gly13Trp) in LAMA3 (Laminin subunit alpha-3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data, published literature, and structural context.
G13W (p.Gly13Trp) variant details
- p.Gly13Trp
- gnomAD 18-23689720-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.178
- REVEL 0.09
- CADD 18.70
- PolyPhen-2 0.72
- SIFT 0.03
- Population evidence available
- Structural context available
- Literature evidence available