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 PRKAR1B:
 
NM_001164758
Mutation details:
10
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NM_001164759
Mutation details:
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NM_001164760
Mutation details:
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NM_001164761
Mutation details:
10
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NM_001164762
Mutation details:
10
records
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10
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10
mutation records.
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NM_002735
Mutation details:
10
records
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1
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10
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10
mutation records.
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