D79G (p.Asp79Gly) variant of MBP (Myelin basic protein)
D79G (p.Asp79Gly) in MBP (Myelin basic protein) 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 and structural context.
D79G (p.Asp79Gly) variant details
- p.Asp79Gly
- gnomAD rs1971696362
- Missense
- Variant Prioritization Score for Impact Estimate 0.14
- REVEL 0.13
- CADD 13.00
- PolyPhen-2 0.00
- SIFT 0.30
- Most common in the REMAINING population (allele frequency 0.00048)
- Structural context available