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 RC3H1:
 
NM_001300850
Mutation details:
16
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NM_001300851
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Mutation details:
16
records
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NM_001300852
Mutation details:
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NM_172071
Mutation details:
16
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