G41R (p.Gly41Arg) variant of VIM (Vimentin)
G41R (p.Gly41Arg) in VIM (Vimentin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.66 / 1. The record also includes population frequency data, published literature, and structural context.
G41R (p.Gly41Arg) variant details
- p.Gly41Arg
- gnomAD 10-17229543-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.664
- REVEL 0.62
- MetaLR 0.63
- MetaSVM 0.29
- CADD 27.60
- PolyPhen-2 0.71
- SIFT 0.23
- Most common in the Finnish in Finland (FIN) population (allele frequency 2e-05)
- Structural context available
- Literature evidence available