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 NF2:
 
NM_000268
Mutation details:
11
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NM_016418
Mutation details:
11
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NM_181825
Mutation details:
11
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NM_181828
Mutation details:
9
records
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NM_181829
Mutation details:
11
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NM_181830
Mutation details:
9
records
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10
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9
mutation records.
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NM_181831
Mutation details:
9
records
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NM_181832
Mutation details:
11
records
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10
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11
mutation records.
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NM_181833
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Mutation details:
3
records
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10
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3
mutation records.
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