G109R (p.Gly109Arg) variant of ABCA3 (Q99758)
G109R (p.Gly109Arg) in ABCA3 (Q99758) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G109R (p.Gly109Arg) variant details
- p.Gly109Arg
- NCI-TCGA Cosmic COSV1000
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available