G19D (p.Gly19Asp) variant of VIM (Vimentin)
G19D (p.Gly19Asp) in VIM (Vimentin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data, published literature, and structural context.
G19D (p.Gly19Asp) variant details
- p.Gly19Asp
- gnomAD 10-17229478-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.512
- REVEL 0.43
- MetaLR 0.68
- MetaSVM 0.57
- CADD 23.00
- PolyPhen-2 0.05
- SIFT 0.16
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available
- Literature evidence available