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 SSH1:
 
NM_001161330
Mutation details:
8
records
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10
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8
mutation records.
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NM_001161331
Mutation details:
8
records
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1
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10
/
8
mutation records.
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1
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NM_018984
Mutation details:
13
records
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10
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13
mutation records.
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