M17T (p.Met17Thr) variant of MAOB (P27338)
M17T (p.Met17Thr) in MAOB (P27338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data and structural context.
M17T (p.Met17Thr) variant details
- p.Met17Thr
- gnomAD rs1332503515
- Missense
- Variant Prioritization Score for Impact Estimate 0.563
- REVEL 0.66
- MetaLR 0.58
- MetaSVM 0.28
- CADD 21.80
- PolyPhen-2 0.01
- SIFT 0.04
- Most common in the REMAINING population (allele frequency 2.2e-05)
- Structural context available