S23G (p.Ser23Gly) variant of KRT2 (P35908)
S23G (p.Ser23Gly) in KRT2 (P35908) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data and structural context.
S23G (p.Ser23Gly) variant details
- p.Ser23Gly
- TOPMed rs1265452262
- gnomAD rs1265452262
- Missense
- Variant Prioritization Score for Impact Estimate 0.427
- REVEL 0.38
- CADD 23.10
- PolyPhen-2 0.02
- SIFT 0.00
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available