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 RAB40C:
 
NM_001172663
Mutation details:
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NM_001172664
Mutation details:
9
records
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9
mutation records.
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NM_001172665
Mutation details:
9
records
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10
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9
mutation records.
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NM_001172666
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Mutation details:
9
records
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1
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10
/
9
mutation records.
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1
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NM_021168
Mutation details:
9
records
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mutation records.
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