P56S (p.Pro56Ser) variant of MMUT (P22033)
P56S (p.Pro56Ser) in MMUT (P22033) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data and structural context.
P56S (p.Pro56Ser) variant details
- p.Pro56Ser
- TOPMed rs1581836281
- Missense
- Variant Prioritization Score for Impact Estimate 0.57
- REVEL 0.54
- CADD 20.80
- PolyPhen-2 0.01
- SIFT 0.21
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available