G11A (p.Gly11Ala) variant of MYL2 (P10916)
G11A (p.Gly11Ala) in MYL2 (P10916) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.22 / 1. The record also includes population frequency data and structural context.
G11A (p.Gly11Ala) variant details
- p.Gly11Ala
- gnomAD rs1216149609
- Missense
- Variant Prioritization Score for Impact Estimate 0.217
- REVEL 0.16
- CADD 9.09
- PolyPhen-2 0.00
- SIFT 0.30
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available