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 TRPT1:
 
NM_001033678
Mutation details:
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NM_001160389
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Mutation details:
5
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5
mutation records.
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NM_001160390
Mutation details:
5
records
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5
mutation records.
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NM_001160392
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Mutation details:
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NM_001160393
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Mutation details:
5
records
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5
mutation records.
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NM_031472
Mutation details:
5
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