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 TP53:
 
NM_000546
Mutation details:
1201
records
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10
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1201
mutation records.
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121
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NM_001126112
Mutation details:
1201
records
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1
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10
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1201
mutation records.
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121
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NM_001126113
Mutation details:
1120
records
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1
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10
/
1120
mutation records.
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112
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NM_001126114
Mutation details:
1117
records
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1
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10
/
1117
mutation records.
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112
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NM_001126115
Mutation details:
1038
records
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1
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10
/
1038
mutation records.
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104
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NM_001126116
Mutation details:
954
records
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1
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10
/
954
mutation records.
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1
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96
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NM_001126117
Mutation details:
957
records
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1
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10
/
957
mutation records.
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96
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NM_001126118
Mutation details:
1183
records
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1
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10
/
1183
mutation records.
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119
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NM_001276695
Mutation details:
1102
records
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1
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10
/
1102
mutation records.
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111
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NM_001276696
Mutation details:
1099
records
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1
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10
/
1099
mutation records.
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1
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110
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NM_001276697
Mutation details:
932
records
Showing
1
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10
/
932
mutation records.
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1
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94
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NM_001276698
Mutation details:
848
records
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1
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10
/
848
mutation records.
Page
1
/
85
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NM_001276699
Mutation details:
851
records
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1
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10
/
851
mutation records.
Page
1
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86
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NM_001276760
Mutation details:
1183
records
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1
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10
/
1183
mutation records.
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1
/
119
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NM_001276761
Mutation details:
1183
records
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1
-
10
/
1183
mutation records.
Page
1
/
119
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