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 A1CF:
 
NM_001198818
Mutation details:
20
records
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10
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20
mutation records.
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NM_001198819
Mutation details:
18
records
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10
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18
mutation records.
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NM_001198820
Mutation details:
18
records
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1
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10
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18
mutation records.
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NM_014576
Mutation details:
20
records
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10
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20
mutation records.
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NM_138932
Mutation details:
20
records
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1
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10
/
20
mutation records.
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NM_138933
Mutation details:
18
records
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1
-
10
/
18
mutation records.
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2
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