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 RIMS1:
 
NM_001168407
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Mutation details:
36
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NM_001168408
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Mutation details:
29
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29
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NM_001168409
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Mutation details:
26
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NM_001168410
Mutation details:
28
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NM_001168411
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Mutation details:
11
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11
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NM_014989
Mutation details:
53
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6
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