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 HM13:
 
NM_178580
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Mutation details:
7
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10
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7
mutation records.
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NM_178581
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Mutation details:
7
records
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10
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7
mutation records.
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NM_030789
Mutation details:
5
records
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5
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NM_178582
Mutation details:
2
records
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1
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10
/
2
mutation records.
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1
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