P33T (p.Pro33Thr) variant of PIM1 (P11309)
P33T (p.Pro33Thr) in PIM1 (P11309) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.45 / 1. The record also includes population frequency data and structural context.
P33T (p.Pro33Thr) variant details
- p.Pro33Thr
- NCI-TCGA Cosmic COSV6516
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.453
- REVEL 0.27
- CADD 22.30
- PolyPhen-2 0.01
- SIFT 0.16
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 8.1e-06)
- Structural context available