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 CRISP2:
 
NM_001142407
Mutation details:
5
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NM_001142408
Mutation details:
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NM_001142417
Mutation details:
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NM_001142435
Mutation details:
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NM_001261822
Mutation details:
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NM_003296
Mutation details:
5
records
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1
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10
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5
mutation records.
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