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 P2RY6:
 
NM_001277204
Mutation details:
6
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NM_001277205
Mutation details:
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NM_001277206
Mutation details:
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NM_001277207
Mutation details:
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NM_001277208
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Mutation details:
6
records
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1
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10
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6
mutation records.
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NM_176796
Mutation details:
6
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NM_176797
Mutation details:
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NM_176798
Mutation details:
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records
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