D37E (p.Asp37Glu) variant of MAOB (P27338)
D37E (p.Asp37Glu) in MAOB (P27338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.49 / 1. The record also includes population frequency data and structural context.
D37E (p.Asp37Glu) variant details
- p.Asp37Glu
- TOPMed rs1171549806
- gnomAD rs1171549806
- Missense
- Variant Prioritization Score for Impact Estimate 0.485
- REVEL 0.54
- MetaLR 0.84
- MetaSVM 0.55
- CADD 17.70
- PolyPhen-2 0.10
- SIFT 0.17
- Most common in the South Asian population (allele frequency 1.9e-05)
- Structural context available