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 SPATA33:
 
NM_001271907
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Mutation details:
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NM_001271908
Mutation details:
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NM_001271909
Mutation details:
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NM_153025
Mutation details:
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NM_001271910
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Mutation details:
1
records
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10
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1
mutation records.
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