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 RAP1GDS1:
 
NM_001100426
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Mutation details:
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NM_001100427
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NM_001100428
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NM_001100429
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NM_001100430
Mutation details:
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NM_021159
Mutation details:
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