N29D (p.Asn29Asp) variant of MAOB (P27338)
N29D (p.Asn29Asp) in MAOB (P27338) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
N29D (p.Asn29Asp) variant details
- p.Asn29Asp
- TOPMed rs1028364289
- Missense
- Variant Prioritization Score for Impact Estimate 0.295
- REVEL 0.27
- MetaLR 0.47
- MetaSVM -0.32
- CADD 17.50
- PolyPhen-2 0.00
- SIFT 0.38
- Most common in the Non-Finnish European population (allele frequency 2.4e-06)
- Structural context available