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 SUPT20H:
 
NM_001014286
Mutation details:
12
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NM_001278480
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Mutation details:
13
records
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NM_001278481
Mutation details:
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NM_001278482
Mutation details:
11
records
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11
mutation records.
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NM_017569
Mutation details:
11
records
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