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 ASTN1:
 
NM_001286164
Mutation details:
52
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NM_004319
Mutation details:
61
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NM_207108
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Mutation details:
52
records
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1
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10
/
52
mutation records.
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1
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6
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