G49R (p.Gly49Arg) variant of CLDN14 (Claudin-14)
G49R (p.Gly49Arg) in CLDN14 (Claudin-14) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G49R (p.Gly49Arg) variant details
- p.Gly49Arg
- NCI-TCGA Cosmic COSV5977
- cosmic curated COSV59775
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available