G87D (p.Gly87Asp) variant of KRT16 (Keratin, type I cytoskeletal 16)
G87D (p.Gly87Asp) in KRT16 (Keratin, type I cytoskeletal 16) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.42 / 1. The record also includes population frequency data and structural context.
G87D (p.Gly87Asp) variant details
- p.Gly87Asp
- Ensembl rs1567745601
- Missense
- Variant Prioritization Score for Impact Estimate 0.42
- REVEL 0.40
- CADD 22.40
- PolyPhen-2 0.69
- SIFT 0.01
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available