F18V (p.Phe18Val) variant of MYL2 (P10916)
F18V (p.Phe18Val) in MYL2 (P10916) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact in the context of in CMH10. The record also includes variant effect predictions and structural context.
F18V (p.Phe18Val) variant details
- p.Phe18Val
- NCI-TCGA Cosmic COSV5740
- cosmic curated COSV57406
- Variant assessed as somatic; moderate impact.
- in CMH10
- Missense
- MetaLR 0.72
- MetaSVM 0.46
- SIFT 0.61
- UniProt: Variant assessed as somatic; moderate impact. (in CMH10)
- Structural context available