I56V (p.Ile56Val) variant of PIM1 (P11309)
I56V (p.Ile56Val) in PIM1 (P11309) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
I56V (p.Ile56Val) variant details
- p.Ile56Val
- Ensembl rs1762266784
- Missense
- Variant Prioritization Score for Impact Estimate 0.127
- REVEL 0.05
- CADD 14.30
- PolyPhen-2 0.00
- SIFT 0.64
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available