A16G (p.Ala16Gly) variant of CALM2 (Calmodulin-2)
A16G (p.Ala16Gly) in CALM2 (Calmodulin-2) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The available variant effect predictions contribute to a CATVariant prioritization score of 0.77 / 1. The record also includes published literature and structural context.
A16G (p.Ala16Gly) variant details
- p.Ala16Gly
- rs1599758635
- ClinGen CA406471673
- ClinVar RCV004577345
- Ensembl rs1599758635
- Uncertain significance
- Missense
- Variant Prioritization Score for Impact Estimate 0.767
- AlphaMissense 0.90
- MetaLR 0.73
- MetaSVM 0.57
- MutPred 0.78
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: Long QT Syndrome Overview. (PMID 20301308)
- Cited in: HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this… (PMID 21810866)