A14P (p.Ala14Pro) variant of PIM1 (P11309)
A14P (p.Ala14Pro) in PIM1 (P11309) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data, published literature, and structural context.
A14P (p.Ala14Pro) variant details
- p.Ala14Pro
- gnomAD 6-37170615-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.218
- REVEL 0.12
- CADD 19.10
- PolyPhen-2 0.00
- SIFT 0.31
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available