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 HIPK1:
 
NM_152696
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Mutation details:
20
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NM_198268
Mutation details:
21
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NM_181358
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Mutation details:
11
records
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11
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NM_198269
Mutation details:
11
records
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1
-
10
/
11
mutation records.
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1
/
2
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Last
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