A33G (p.Ala33Gly) variant of SFTPB (P07988)
A33G (p.Ala33Gly) 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.
A33G (p.Ala33Gly) variant details
- p.Ala33Gly
- NCI-TCGA Cosmic COSV6089
- cosmic curated COSV60894
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available