S38A (p.Ser38Ala) variant of NLRP1 (Q9C000)
S38A (p.Ser38Ala) in NLRP1 (Q9C000) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
S38A (p.Ser38Ala) variant details
- p.Ser38Ala
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.