D39N (p.Asp39Asn) variant of CLCN5 (P51795)
D39N (p.Asp39Asn) in CLCN5 (P51795) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D39N (p.Asp39Asn) variant details
- p.Asp39Asn
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available