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 FCGR3B:
 
NM_000570
Mutation details:
9
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NM_001244753
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Mutation details:
9
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NM_001271035
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Mutation details:
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NM_001271036
Mutation details:
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NM_001271037
Mutation details:
4
records
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4
mutation records.
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