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BIOMARKER:
MLH1 mutation
i
Other names:
MLH1, COCA2, FCC2, HNPCC, HNPCC2, MutL homolog 1
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Entrez ID:
4292
Related biomarkers:
Mutation
CNA
Others
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Associations
(6)
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1year
IHC result with absence of MLH1 & PMS2. Possible explanations include (most likely to least): 1. MLH1 promoter hypermethylation 2. Double somatic MLH1 mutations 3. Lynch syndrome All other abnormal IHC findings in CRC are more likely LS than DS. #ColorectalCancerAwarenessMonth (@HHampel1)
1 year ago
PMS2 (PMS1 protein homolog 2)
|
MLH1 mutation
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