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 FGFR2:
 
NM_000141
Mutation details:
14
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NM_001144913
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Mutation details:
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NM_001144914
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Mutation details:
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NM_001144915
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Mutation details:
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NM_001144916
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Mutation details:
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NM_001144918
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Mutation details:
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NM_001144919
Mutation details:
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NM_022970
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Mutation details:
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NM_023029
Mutation details:
14
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NM_001144917
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Mutation details:
11
records
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11
mutation records.
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