ESCCdb: An Integrated Database for Esophageal Squamous Cell Carcinoma
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Consensus DEGs
Recurrent Mutations
Significant CNV
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Somatic mutations of CTNND2:
 
NM_001288715
Mutation details:
44
records
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NM_001288716
Mutation details:
38
records
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NM_001288717
Mutation details:
34
records
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NM_001332
Mutation details:
51
records
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6
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