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 BFSP1:
 
NM_001161705
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Mutation details:
8
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NM_001195
Mutation details:
11
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NM_001278606
Mutation details:
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NM_001278607
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Mutation details:
8
records
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1
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10
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8
mutation records.
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1
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NM_001278608
Mutation details:
7
records
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1
-
10
/
7
mutation records.
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1
/
1
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Last
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