R13G (p.Arg13Gly) variant of PIM1 (P11309)
R13G (p.Arg13Gly) in PIM1 (P11309) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data, published literature, and structural context.
R13G (p.Arg13Gly) variant details
- p.Arg13Gly
- gnomAD 6-37170612-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.308
- REVEL 0.12
- CADD 22.60
- PolyPhen-2 0.09
- SIFT 0.35
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available