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 ARHGEF12:
 
NM_001198665
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Mutation details:
13
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NM_001301084
Mutation details:
12
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NM_015313
Mutation details:
13
records
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