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 SVIL:
 
NM_021738
Mutation details:
31
records
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NM_003174
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Mutation details:
27
records
Showing
1
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10
/
27
mutation records.
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1
/
3
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