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 TGFBR2:
NM_001024847
Mutation details:
31
records
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31
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NM_003242
Mutation details:
31
records
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1
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10
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31
mutation records.
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4
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