N7S (p.Asn7Ser) variant of PIM1 (P11309)
N7S (p.Asn7Ser) in PIM1 (P11309) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and structural context.
N7S (p.Asn7Ser) variant details
- p.Asn7Ser
- gnomAD rs1215548229
- Missense
- Variant Prioritization Score for Impact Estimate 0.256
- REVEL 0.10
- CADD 20.90
- PolyPhen-2 0.03
- SIFT 0.11
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available