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 NRG1:
 
NM_013959
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Mutation details:
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NM_013956
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Mutation details:
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NM_013957
Mutation details:
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NM_013964
Mutation details:
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NM_001159996
Mutation details:
7
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NM_001160004
Mutation details:
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NM_001160008
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NM_013960
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Mutation details:
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NM_013962
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Mutation details:
8
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NM_001160002
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Mutation details:
5
records
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5
mutation records.
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NM_001160005
Mutation details:
3
records
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3
mutation records.
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NM_001160007
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Mutation details:
3
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3
mutation records.
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NM_004495
Mutation details:
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NM_013958
Mutation details:
5
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