A51T (p.Ala51Thr) variant of MYPN (Myopalladin)
A51T (p.Ala51Thr) in MYPN (Myopalladin) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Dilated cardiomyopathy 1KK; Cardiovascular phenotype. The record also includes structural context.
A51T (p.Ala51Thr) variant details
- p.Ala51Thr
- rs2495460693
- ClinGen CA377103708
- ClinVar RCV003055119
- ClinVar RCV004983279
- Uncertain significance
- Dilated cardiomyopathy 1KK; Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Dilated cardiomyopathy 1KK; Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available