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 SLFN11:
 
NM_001104587
Mutation details:
11
records
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1
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10
/
11
mutation records.
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NM_001104588
Mutation details:
11
records
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1
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10
/
11
mutation records.
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2
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NM_001104589
Mutation details:
11
records
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1
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10
/
11
mutation records.
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NM_001104590
Mutation details:
11
records
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1
-
10
/
11
mutation records.
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/
2
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NM_152270
Mutation details:
11
records
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1
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10
/
11
mutation records.
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2
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