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 PIWIL2:
NM_001135721
Mutation details:
11
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11
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NM_018068
Mutation details:
11
records
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1
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10
/
11
mutation records.
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2
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