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 PHF19:
 
NM_001009936
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Mutation details:
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NM_001286840
Mutation details:
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NM_001286843
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Mutation details:
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NM_015651
Mutation details:
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NM_001286842
Mutation details:
4
records
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