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 FOXM1:
 
NM_001243088
Mutation details:
9
records
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mutation records.
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NM_001243089
Mutation details:
9
records
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10
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9
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NM_021953
Mutation details:
9
records
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9
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NM_202002
Mutation details:
9
records
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10
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9
mutation records.
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NM_202003
Mutation details:
9
records
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1
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10
/
9
mutation records.
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