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 NR3C1:
 
NM_000176
Mutation details:
7
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NM_001018074
Mutation details:
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NM_001018075
Mutation details:
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NM_001018076
Mutation details:
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NM_001018077
Mutation details:
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NM_001020825
Mutation details:
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NM_001024094
Mutation details:
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NM_001204258
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Mutation details:
7
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NM_001204259
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Mutation details:
7
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7
mutation records.
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NM_001204260
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Mutation details:
7
records
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7
mutation records.
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NM_001204261
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Mutation details:
7
records
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7
mutation records.
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NM_001204262
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Mutation details:
3
records
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NM_001204263
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Mutation details:
3
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3
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NM_001204264
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Mutation details:
3
records
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3
mutation records.
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NM_001204265
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Mutation details:
7
records
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10
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7
mutation records.
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