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 C12orf43:
 
NM_001286191
Mutation details:
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NM_001286192
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Mutation details:
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5
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NM_001286195
Mutation details:
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NM_001286196
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Mutation details:
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5
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NM_001286197
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Mutation details:
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mutation records.
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NM_001286198
Mutation details:
2
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NM_022895
Mutation details:
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