Q79H (p.Gln79His) variant of MAPK3 (P27361)
Q79H (p.Gln79His) in MAPK3 (P27361) 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 0.30 / 1. The record also includes population frequency data and structural context.
Q79H (p.Gln79His) variant details
- p.Gln79His
- ExAC rs778192562
- TOPMed rs778192562
- gnomAD rs778192562
- NCI-TCGA Cosmic COSV9953
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.304
- REVEL 0.20
- CADD 21.00
- PolyPhen-2 0.07
- SIFT 0.21
- UniProt: Variant assessed as somatic; moderate impact.
- Population evidence available
- Structural context available