M55T (p.Met55Thr) variant of MAPK3 (P27361)
M55T (p.Met55Thr) in MAPK3 (P27361) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not specified. The available variant effect predictions contribute to a CATVariant prioritization score of 0.39 / 1. The record also includes population frequency data and structural context.
M55T (p.Met55Thr) variant details
- p.Met55Thr
- rs889768664
- ClinGen CA280416299
- ClinVar RCV002247964
- gnomAD rs889768664
- Uncertain significance
- not specified
- Missense
- Variant Prioritization Score for Impact Estimate 0.395
- REVEL 0.31
- CADD 22.90
- PolyPhen-2 0.03
- SIFT 0.16
- ClinVar: Uncertain significance (not specified)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 4.5e-05)
- Structural context available