G110C (p.Gly110Cys) variant of MYH7 (Myosin-7)
G110C (p.Gly110Cys) in MYH7 (Myosin-7) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Cardiomyopathy. The available variant effect predictions contribute to a CATVariant prioritization score of 0.48 / 1. The record also includes population frequency data, published literature, and structural context.
G110C (p.Gly110Cys) variant details
- p.Gly110Cys
- rs763893822
- ClinGen CA389053066
- ClinVar RCV003532734
- ExAC rs763893822
- Uncertain significance
- Cardiomyopathy
- Missense
- Variant Prioritization Score for Impact Estimate 0.483
- REVEL 0.36
- ESM-1b 1.00
- AlphaMissense 0.15
- MetaLR 0.67
- MetaSVM 0.47
- CADD 22.90
- ClinVar: Uncertain significance (Cardiomyopathy)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Cited in: HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this… (PMID 21810866)