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 INPP4B:
NM_001101669
Mutation details:
17
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NM_003866
Mutation details:
17
records
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1
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10
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17
mutation records.
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2
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