A26V (p.Ala26Val) variant of PIM1 (P11309)
A26V (p.Ala26Val) in PIM1 (P11309) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data, published literature, and structural context.
A26V (p.Ala26Val) variant details
- p.Ala26Val
- gnomAD 6-37170652-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.321
- REVEL 0.04
- CADD 22.40
- PolyPhen-2 0.00
- SIFT 0.32
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available
- Literature evidence available