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 HELLS:
 
NM_001289067
Mutation details:
20
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NM_001289068
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Mutation details:
19
records
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10
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19
mutation records.
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NM_001289069
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Mutation details:
13
records
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10
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13
mutation records.
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NM_001289070
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Mutation details:
18
records
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10
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18
mutation records.
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NM_001289071
Mutation details:
16
records
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16
mutation records.
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NM_001289072
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Mutation details:
12
records
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10
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12
mutation records.
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NM_001289073
Mutation details:
16
records
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10
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16
mutation records.
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NM_001289074
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Mutation details:
8
records
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10
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8
mutation records.
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NM_001289075
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Mutation details:
8
records
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1
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10
/
8
mutation records.
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1
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NM_018063
Mutation details:
19
records
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10
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19
mutation records.
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