N18S (p.Asn18Ser) variant of PIM1 (P11309)
N18S (p.Asn18Ser) in PIM1 (P11309) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data, published literature, and structural context.
N18S (p.Asn18Ser) variant details
- p.Asn18Ser
- gnomAD 6-37170628-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.107
- REVEL 0.10
- CADD 5.43
- PolyPhen-2 0.00
- SIFT 0.74
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available