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 DNAH9:
 
NM_001372
Mutation details:
74
records
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10
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74
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8
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NM_004662
Mutation details:
21
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21
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3
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