L49H (p.Leu49His) variant of MYL2 (P10916)
L49H (p.Leu49His) in MYL2 (P10916) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.04 / 1. The record also includes population frequency data, published literature, and structural context.
L49H (p.Leu49His) variant details
- p.Leu49His
- gnomAD 12-110914323-A-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.0424
- CADD 0.26
- SIFT 0.00
- Population evidence available
- Structural context available
- Literature evidence available