Annotation Detail
Information
- Associated Genes
- MGMT
- Associated Variants
-
MGMT p.Lys178Arg (p.K178R)
(
ENST00000306010.8,
ENST00000651593.1 )
MGMT p.Lys178Arg (p.K178R) ( ENST00000306010.8, ENST00000651593.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_002412.5(MGMT):c.533A>G (p.Lys178Arg) AND not provided
- ClinVar Allele ID
- 1222036
- ClinVar RefSeq Alternation Syntax
- NM_002412.5:c.533A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2019-10-07
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001616833
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs