I26N (p.Ile26Asn) variant of CLDN14 (Claudin-14)
I26N (p.Ile26Asn) in CLDN14 (Claudin-14) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
I26N (p.Ile26Asn) variant details
- p.Ile26Asn
- rs2517047770
- ClinGen CA409884810
- ClinVar RCV003129506
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available