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 PYCR1:
 
NM_153824
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Mutation details:
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NM_001282279
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NM_001282280
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NM_001282281
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NM_006907
Mutation details:
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