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 FCHO1:
 
NM_001161357
Mutation details:
18
records
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18
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NM_001161358
Mutation details:
18
records
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10
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18
mutation records.
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NM_001161359
Mutation details:
18
records
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1
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10
/
18
mutation records.
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2
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NM_015122
Mutation details:
18
records
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10
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18
mutation records.
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