P98S (p.Pro98Ser) variant of MAOB (P27338)
P98S (p.Pro98Ser) in MAOB (P27338) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data and structural context.
P98S (p.Pro98Ser) variant details
- p.Pro98Ser
- rs1426305009
- NCI-TCGA Cosmic COSV1009
- gnomAD rs1426305009
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.156
- REVEL 0.08
- MetaLR 0.02
- MetaSVM -1.00
- CADD 15.70
- PolyPhen-2 0.02
- SIFT 0.06
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available