G38E (p.Gly38Glu) variant of KRT16 (Keratin, type I cytoskeletal 16)
G38E (p.Gly38Glu) in KRT16 (Keratin, type I cytoskeletal 16) 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.
G38E (p.Gly38Glu) variant details
- p.Gly38Glu
- rs1216992535
- ClinGen CA399496534
- ClinVar RCV001991207
- gnomAD rs1216992535
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available