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 CHN2:
 
NM_001039936
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Mutation details:
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NM_001293069
Mutation details:
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NM_001293070
Mutation details:
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NM_001293071
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Mutation details:
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NM_001293072
Mutation details:
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NM_001293076
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Mutation details:
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NM_001293077
Mutation details:
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mutation records.
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NM_001293078
Mutation details:
6
records
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6
mutation records.
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NM_001293079
Mutation details:
6
records
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10
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6
mutation records.
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NM_001293080
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Mutation details:
7
records
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10
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7
mutation records.
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NM_004067
Mutation details:
8
records
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8
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NM_001293073
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Mutation details:
5
records
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10
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5
mutation records.
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NM_001293075
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Mutation details:
5
records
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10
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5
mutation records.
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NM_001293081
Mutation details:
4
records
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10
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4
mutation records.
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