S27G (p.Ser27Gly) variant of VIM (Vimentin)
S27G (p.Ser27Gly) in VIM (Vimentin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data and structural context.
S27G (p.Ser27Gly) variant details
- p.Ser27Gly
- ExAC rs775343323
- TOPMed rs775343323
- gnomAD rs775343323
- Missense
- Variant Prioritization Score for Impact Estimate 0.285
- REVEL 0.25
- CADD 21.80
- PolyPhen-2 0.00
- SIFT 0.13
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available