G42R (p.Gly42Arg) variant of MYL2 (P10916)
G42R (p.Gly42Arg) in MYL2 (P10916) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data, published literature, and structural context.
G42R (p.Gly42Arg) variant details
- p.Gly42Arg
- rs377275311
- gnomAD 12-110914321-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.0555
- CADD 0.00
- SIFT 0.38
- Most common in the REMAINING population (allele frequency 0.00096)
- Structural context available
- Literature evidence available