G82R (p.Gly82Arg) variant of KRT17 (Keratin, type I cytoskeletal 17)
G82R (p.Gly82Arg) in KRT17 (Keratin, type I cytoskeletal 17) 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.
G82R (p.Gly82Arg) variant details
- p.Gly82Arg
- rs2543827877
- ClinGen CA399512694
- NCI-TCGA Cosmic COSV6086
- ClinVar RCV003863430
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available