V31G (p.Val31Gly) variant of KRT10 (Keratin, type I cytoskeletal 10)
V31G (p.Val31Gly) in KRT10 (Keratin, type I cytoskeletal 10) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data.
V31G (p.Val31Gly) variant details
- p.Val31Gly
- TOPMed rs1435728074
- gnomAD rs1435728074
- Missense
- Variant Prioritization Score for Impact Estimate 0.197
- REVEL 0.16
- CADD 9.94
- PolyPhen-2 0.00
- SIFT 0.00
- Most common in the HGDP:FRENCH population (allele frequency 0.019)