M20T (p.Met20Thr) variant of MYL2 (P10916)
M20T (p.Met20Thr) in MYL2 (P10916) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes population frequency data and structural context.
M20T (p.Met20Thr) variant details
- p.Met20Thr
- ExAC rs113167834
- gnomAD rs113167834
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available