G121S (p.Gly121Ser) variant of KRT10 (Keratin, type I cytoskeletal 10)
G121S (p.Gly121Ser) in KRT10 (Keratin, type I cytoskeletal 10) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.19 / 1. The record also includes population frequency data.
G121S (p.Gly121Ser) variant details
- p.Gly121Ser
- rs568226045
- NCI-TCGA Cosmic COSV5408
- gnomAD rs568226045
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.189
- REVEL 0.18
- AlphaMissense 0.10
- MetaLR 0.15
- MetaSVM -0.90
- CADD 0.00
- PolyPhen-2 0.96
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the REMAINING population (allele frequency 0.00048)