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 ATP2C1:
 
NM_001001485
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NM_001001486
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NM_001001487
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NM_001199179
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NM_001199180
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NM_001199181
Mutation details:
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NM_001199182
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NM_001199183
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NM_001199184
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NM_001199185
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Mutation details:
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NM_014382
Mutation details:
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