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 FGFR1:
 
NM_001174063
Mutation details:
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NM_001174064
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Mutation details:
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NM_001174065
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Mutation details:
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NM_001174066
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Mutation details:
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NM_001174067
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Mutation details:
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NM_015850
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Mutation details:
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NM_023105
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NM_023106
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Mutation details:
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NM_023110
Mutation details:
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