P18R (p.Pro18Arg) variant of VIM (Vimentin)
P18R (p.Pro18Arg) in VIM (Vimentin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data and structural context.
P18R (p.Pro18Arg) variant details
- p.Pro18Arg
- TOPMed rs11545549
- gnomAD rs11545549
- Missense
- Variant Prioritization Score for Impact Estimate 0.294
- REVEL 0.23
- CADD 21.70
- Most common in the Latino/Admixed American population (allele frequency 6.5e-05)
- Structural context available