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 PLEKHG4:
 
NM_001129727
Mutation details:
16
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NM_001129728
Mutation details:
16
records
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1
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10
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16
mutation records.
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2
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NM_001129729
Mutation details:
16
records
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1
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10
/
16
mutation records.
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2
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NM_001129731
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Mutation details:
14
records
Showing
1
-
10
/
14
mutation records.
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1
/
2
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