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 SCO2:
 
NM_001169109
Mutation details:
8
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NM_001169110
Mutation details:
8
records
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1
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10
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8
mutation records.
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NM_001169111
Mutation details:
8
records
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1
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10
/
8
mutation records.
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NM_005138
Mutation details:
8
records
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1
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10
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8
mutation records.
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