R58= variant of MYL2 (P10916)
R58= in MYL2 (P10916) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; low impact in the context of in CMH10. The record also includes population frequency data and structural context.
R58= variant details
- rs756671869
- NCI-TCGA Cosmic COSV5740
- NCI-TCGA Cosmic COSV9996
- Variant assessed as somatic; low impact.
- in CMH10
- Missense
- UniProt: Variant assessed as somatic; low impact. (in CMH10)
- Population evidence available
- Structural context available