S69F (p.Ser69Phe) variant of CLDN14 (Claudin-14)
S69F (p.Ser69Phe) in CLDN14 (Claudin-14) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes structural context.
S69F (p.Ser69Phe) variant details
- p.Ser69Phe
- cosmic curated COSV59773
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available