G37V (p.Gly37Val) variant of KRT16 (Keratin, type I cytoskeletal 16)
G37V (p.Gly37Val) in KRT16 (Keratin, type I cytoskeletal 16) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data and structural context.
G37V (p.Gly37Val) variant details
- p.Gly37Val
- ExAC rs762970825
- gnomAD rs762970825
- Missense
- Variant Prioritization Score for Impact Estimate 0.408
- REVEL 0.32
- CADD 14.40
- PolyPhen-2 0.28
- SIFT 0.28
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available