P111S (p.Pro111Ser) variant of NOD1 (Q9Y239)
P111S (p.Pro111Ser) in NOD1 (Q9Y239) 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 0.24 / 1. The record also includes population frequency data and structural context.
P111S (p.Pro111Ser) variant details
- p.Pro111Ser
- NCI-TCGA Cosmic COSV5611
- TOPMed rs1786215119
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.244
- REVEL 0.15
- CADD 18.60
- PolyPhen-2 0.35
- SIFT 0.07
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)
- Structural context available