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 HHLA2:
 
NM_001282556
Mutation details:
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NM_001282557
Mutation details:
10
records
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NM_001282558
Mutation details:
10
records
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NM_001282559
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Mutation details:
9
records
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1
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10
/
9
mutation records.
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NM_007072
Mutation details:
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