H38D (p.His38Asp) variant of PRKCH (Protein kinase C eta type)
H38D (p.His38Asp) in PRKCH (Protein kinase C eta type) 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, published literature, and structural context.
H38D (p.His38Asp) variant details
- p.His38Asp
- gnomAD 14-61322213-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.143
- REVEL 0.10
- ESM-1b 0.00
- AlphaMissense 0.10
- MetaLR 0.11
- MetaSVM -0.99
- CADD 9.70
- Population evidence available
- Structural context available
- Literature evidence available