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 FAM13C:
 
NM_001001971
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Mutation details:
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NM_198215
Mutation details:
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NM_001143773
Mutation details:
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NM_001166698
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Mutation details:
2
records
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2
mutation records.
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