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 BARD1:
 
NM_000465
Mutation details:
21
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NM_001282543
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Mutation details:
21
records
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NM_001282545
Mutation details:
7
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NM_001282548
Mutation details:
7
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NM_001282549
Mutation details:
5
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