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 RNF17:
NM_001184993
Mutation details:
15
records
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10
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15
mutation records.
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NM_031277
Mutation details:
15
records
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10
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15
mutation records.
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