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 SCYL1:
 
NM_001048218
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Mutation details:
18
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NM_020680
Mutation details:
19
records
Showing
1
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10
/
19
mutation records.
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2
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Download Data