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 ARHGAP30:
 
NM_001025598
Mutation details:
25
records
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10
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25
mutation records.
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NM_001287600
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Mutation details:
22
records
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22
mutation records.
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NM_001287602
Mutation details:
22
records
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10
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22
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NM_181720
Mutation details:
19
records
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