C18G (p.Cys18Gly) variant of CHEK2 (O96017)
C18G (p.Cys18Gly) in CHEK2 (O96017) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome; Familial cancer of breast. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes published literature and structural context.
C18G (p.Cys18Gly) variant details
- p.Cys18Gly
- rs2054336674
- ClinGen CA411091861
- ClinVar RCV001187827
- ClinVar RCV006465657
- Uncertain significance
- Hereditary cancer-predisposing syndrome; Familial cancer of breast
- Missense
- Variant Prioritization Score for Impact Estimate 0.474
- AlphaMissense 0.06
- MetaLR 0.61
- MetaSVM -0.32
- PolyPhen-2 0.01
- SIFT 0.04
- MutPred 0.23
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; Familial cancer of brea)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available
- Cited in: Genetic cancer risk assessment and counseling: recommendations of the national society of genetic counselors. (PMID 15604628)
- Cited in: Risk assessment and genetic counseling for hereditary breast and ovarian cancer: recommendations of the National… (PMID 17508274)