P8T (p.Pro8Thr) variant of MYL3 (Myosin light chain 3)
P8T (p.Pro8Thr) in MYL3 (Myosin light chain 3) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hypertrophic cardiomyopathy. The record also includes structural context.
P8T (p.Pro8Thr) variant details
- p.Pro8Thr
- rs2544972061
- ClinGen CA352499909
- ClinVar RCV003749936
- Uncertain significance
- Hypertrophic cardiomyopathy
- Missense
- ClinVar: Uncertain significance (Hypertrophic cardiomyopathy)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available