G41C (p.Gly41Cys) variant of VIM (Vimentin)
G41C (p.Gly41Cys) in VIM (Vimentin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.75 / 1. The record also includes population frequency data, published literature, and structural context.
G41C (p.Gly41Cys) variant details
- p.Gly41Cys
- gnomAD 10-17229543-G-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.751
- REVEL 0.74
- MetaLR 0.68
- MetaSVM 0.47
- CADD 32.00
- PolyPhen-2 0.91
- SIFT 0.02
- Most common in the Finnish in Finland (FIN) population (allele frequency 2e-05)
- Structural context available
- Literature evidence available