P119S (p.Pro119Ser) variant of NLRP1 (Q9C000)
P119S (p.Pro119Ser) in NLRP1 (Q9C000) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
P119S (p.Pro119Ser) variant details
- p.Pro119Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.