V38M (p.Val38Met) variant of MAPK3 (P27361)
V38M (p.Val38Met) in MAPK3 (P27361) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The available variant effect predictions contribute to a CATVariant prioritization score of 0.35 / 1. The record also includes population frequency data and structural context.
V38M (p.Val38Met) variant details
- p.Val38Met
- cosmic curated COSV10730
- TOPMed rs1394035337
- gnomAD rs1394035337
- Uncertain significance
- Missense
- Variant Prioritization Score for Impact Estimate 0.353
- REVEL 0.22
- CADD 25.60
- PolyPhen-2 0.81
- SIFT 0.00
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available