A13D (p.Ala13Asp) variant of MYL2 (P10916)
A13D (p.Ala13Asp) 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.
A13D (p.Ala13Asp) variant details
- p.Ala13Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- in CMH10
- Missense
- MetaLR 0.47
- MetaSVM -0.10
- SIFT 0.03
- UniProt: Variant assessed as somatic; moderate impact. (in CMH10)
- Structural context available