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 CHST12:
NM_001243794
Mutation details:
7
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NM_001243795
Mutation details:
7
records
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10
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7
mutation records.
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NM_018641
Mutation details:
7
records
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10
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7
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