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 SAMD9L:
 
NM_001303496
Mutation details:
58
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NM_001303497
Mutation details:
58
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NM_001303498
Mutation details:
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NM_001303500
Mutation details:
58
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NM_152703
Mutation details:
58
records
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