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 ARHGAP39:
 
NM_001308207
Mutation details:
28
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NM_001308208
Mutation details:
28
records
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NM_025251
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Mutation details:
29
records
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1
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10
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29
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3
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