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 LOXHD1:
 
NM_144612
Mutation details:
41
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NM_001145472
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Mutation details:
10
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NM_001145473
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Mutation details:
4
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4
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NM_001173129
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Mutation details:
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NM_001308013
Mutation details:
6
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