P119H (p.Pro119His) variant of NLRP1 (Q9C000)
P119H (p.Pro119His) in NLRP1 (Q9C000) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
P119H (p.Pro119His) variant details
- p.Pro119His
- NCI-TCGA Cosmic COSV9933
- cosmic curated COSV99332
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.