M1T (p.Met1Thr) variant of MYPN (Myopalladin)
M1T (p.Met1Thr) in MYPN (Myopalladin) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
M1T (p.Met1Thr) variant details
- p.Met1Thr
- rs2495459067
- ClinGen CA377103399
- ClinVar RCV003456704
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available