G11V (p.Gly11Val) variant of MYL2 (P10916)
G11V (p.Gly11Val) 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.
G11V (p.Gly11Val) variant details
- p.Gly11Val
- NCI-TCGA Cosmic COSV5740
- cosmic curated COSV57408
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.35
- MetaSVM -0.43
- SIFT 0.15
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available