I89V (p.Ile89Val) variant of MAPK1 (P28482)
I89V (p.Ile89Val) in MAPK1 (P28482) 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 0.33 / 1. The record also includes population frequency data, experimental measurements, and structural context.
I89V (p.Ile89Val) variant details
- p.Ile89Val
- NCI-TCGA TCGA novel
- gnomAD rs2069153808
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.331
- REVEL 0.22
- CADD 22.40
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Finnish in Finland (FIN) population (allele frequency 9.4e-05)
- Structural context available
- MAPK1 DOX: score 7.48