Annotation Detail
Information
- Associated Genes
- CHEK2
- Associated Variants
-
CHEK2 p.Arg160Gly (p.R160G)
(
ENST00000348295.7,
ENST00000382580.6,
ENST00000402731.6,
ENST00000403642.5,
ENST00000404276.6,
ENST00000405598.5,
ENST00000425190.7,
ENST00000649563.1,
ENST00000650281.1 )
CHEK2 p.Arg160Gly (p.R160G) ( ENST00000348295.7, ENST00000382580.6, ENST00000402731.6, ENST00000403642.5, ENST00000404276.6, ENST00000405598.5, ENST00000425190.7, ENST00000649563.1, ENST00000650281.1 ) - Associated Disease
- Malignant tumor of prostate Familial cancer of breast colorectal cancer bone osteosarcoma Li-Fraumeni syndrome 2
- Source Database
- ClinVar
- Description
- NM_007194.4(CHEK2):c.349A>G (p.Arg117Gly) AND multiple conditions
- ClinVar Allele ID
- 133528
- ClinVar RefSeq Alternation Syntax
- NM_001349956.2:c.349A>G
- ClinVar RefSeq Alternation Syntax
- NM_145862.2:c.349A>G
- ClinVar RefSeq Alternation Syntax
- NM_001257387.2:c.-429A>G
- ClinVar RefSeq Alternation Syntax
- NM_001005735.2:c.478A>G
- ClinVar RefSeq Alternation Syntax
- NM_007194.4:c.349A>G
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2021-12-08
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002498498
- ClinVar Disease
- Bone osteosarcoma
- ClinVar Disease
- Li-Fraumeni syndrome 2
- ClinVar Disease
- Malignant tumor of prostate
- ClinVar Disease
- Colorectal cancer
- ClinVar Disease
- Familial cancer of breast
- Observed Origin Sample
- unknown
Drugs