Annotation Detail
Information
- Associated Genes
- CHEK2
- Associated Variants
-
CHEK2 p.Thr519Met (p.T519M)
(
ENST00000404276.6,
ENST00000425190.7,
ENST00000403642.5,
ENST00000348295.7,
ENST00000405598.5,
ENST00000402731.6,
ENST00000464581.6,
ENST00000382580.6,
ENST00000650281.1,
ENST00000649563.1 )
CHEK2 p.Thr519Met (p.T519M) ( ENST00000348295.7, ENST00000382580.6, ENST00000402731.6, ENST00000403642.5, ENST00000404276.6, ENST00000405598.5, ENST00000425190.7, ENST00000464581.6, ENST00000649563.1, ENST00000650281.1 ) - Associated Disease
- colorectal cancer
- Source Database
- ClinVar
- Description
- NM_007194.4(CHEK2):c.1427C>T (p.Thr476Met) AND Colorectal cancer
- ClinVar Allele ID
- 133517
- ClinVar RefSeq Alternation Syntax
- NM_001257387.2:c.764C>T
- ClinVar RefSeq Alternation Syntax
- NM_007194.4:c.1427C>T
- ClinVar RefSeq Alternation Syntax
- NM_001005735.2:c.1556C>T
- ClinVar RefSeq Alternation Syntax
- NM_001349956.2:c.1226C>T
- ClinVar RefSeq Alternation Syntax
- NM_145862.2:c.1340C>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2016-06-14
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000259876
- ClinVar Disease
- Colorectal cancer
- Observed Origin Sample
- germline
Drugs