R40W (p.Arg40Trp) variant of MYL2 (P10916)
R40W (p.Arg40Trp) in MYL2 (P10916) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes variant effect predictions and structural context.
R40W (p.Arg40Trp) variant details
- p.Arg40Trp
- NCI-TCGA Cosmic COSV5740
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.20
- MetaSVM -0.83
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available