P138S (p.Pro138Ser) variant of MAOB (P27338)
P138S (p.Pro138Ser) in MAOB (P27338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.82 / 1. The record also includes population frequency data and structural context.
P138S (p.Pro138Ser) variant details
- p.Pro138Ser
- gnomAD rs1440909955
- Missense
- Variant Prioritization Score for Impact Estimate 0.816
- REVEL 0.87
- MetaLR 0.89
- MetaSVM 0.91
- CADD 24.90
- PolyPhen-2 0.79
- SIFT 0.03
- Most common in the Non-Finnish European population (allele frequency 8.4e-06)
- Structural context available