G34S (p.Gly34Ser) variant of KRT17 (Keratin, type I cytoskeletal 17)
G34S (p.Gly34Ser) in KRT17 (Keratin, type I cytoskeletal 17) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
G34S (p.Gly34Ser) variant details
- p.Gly34Ser
- ExAC rs758929957
- TOPMed rs758929957
- gnomAD rs758929957
- Missense
- Variant Prioritization Score for Impact Estimate 0.116
- REVEL 0.11
- CADD 8.55
- PolyPhen-2 0.00
- SIFT 0.42
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)
- Structural context available