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 ANKRD11:
 
NM_001256182
Mutation details:
32
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NM_001256183
Mutation details:
32
records
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1
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10
/
32
mutation records.
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4
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NM_013275
Mutation details:
32
records
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1
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10
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32
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4
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