D118G (p.Asp118Gly) variant of SFTPB (P07988)
D118G (p.Asp118Gly) in SFTPB (P07988) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D118G (p.Asp118Gly) variant details
- p.Asp118Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available