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 PLEKHB2:
 
NM_001100623
Mutation details:
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NM_001267062
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NM_001267063
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NM_001267064
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NM_001267065
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NM_001267066
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NM_001267067
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NM_001267068
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NM_017958
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NM_001309448
Mutation details:
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NM_001309450
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NM_001309451
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NM_001309452
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