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 PHF20L1:
 
NM_001277196
Mutation details:
26
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NM_016018
Mutation details:
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NM_198513
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Mutation details:
7
records
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