R97G (p.Arg97Gly) variant of ACTC1 (Actin, alpha cardiac muscle 1)
R97G (p.Arg97Gly) in ACTC1 (Actin, alpha cardiac muscle 1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact in the context of in CMH11. The record also includes structural context.
R97G (p.Arg97Gly) variant details
- p.Arg97Gly
- NCI-TCGA Cosmic COSV5175
- NCI-TCGA Cosmic COSV9929
- Variant assessed as somatic; moderate impact.
- in CMH11
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in CMH11)
- Structural context available