E13Q (p.Glu13Gln) variant of MAPK3 (P27361)
E13Q (p.Glu13Gln) in MAPK3 (P27361) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data and structural context.
E13Q (p.Glu13Gln) variant details
- p.Glu13Gln
- TOPMed rs1461921044
- gnomAD rs1461921044
- Missense
- Variant Prioritization Score for Impact Estimate 0.324
- REVEL 0.21
- CADD 20.30
- PolyPhen-2 0.00
- SIFT 0.56
- Most common in the 1KG:STU population (allele frequency 0.0063)
- Structural context available