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 ATP6V1H:
 
NM_015941
Mutation details:
9
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NM_213619
Mutation details:
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NM_213620
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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