L41I (p.Leu41Ile) variant of CLDN14 (Claudin-14)
L41I (p.Leu41Ile) 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.
L41I (p.Leu41Ile) variant details
- p.Leu41Ile
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available