G39S (p.Gly39Ser) variant of KRT3 (Keratin, type II cytoskeletal 3)
G39S (p.Gly39Ser) in KRT3 (Keratin, type II cytoskeletal 3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data and structural context.
G39S (p.Gly39Ser) variant details
- p.Gly39Ser
- 1000Genomes rs202180550
- ExAC rs202180550
- gnomAD rs202180550
- Missense
- Variant Prioritization Score for Impact Estimate 0.138
- REVEL 0.20
- CADD 0.06
- PolyPhen-2 0.00
- SIFT 0.34
- Most common in the African/African-American population (allele frequency 0.00012)
- Structural context available