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 FAM222B:
 
NM_001077498
Mutation details:
3
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NM_001288631
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Mutation details:
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NM_001288632
Mutation details:
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NM_001288633
Mutation details:
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NM_001288634
Mutation details:
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records
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NM_001288635
Mutation details:
3
records
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NM_001288636
Mutation details:
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NM_001288637
Mutation details:
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records
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NM_001288638
Mutation details:
3
records
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3
mutation records.
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NM_001288639
Mutation details:
3
records
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3
mutation records.
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NM_001288640
Mutation details:
3
records
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1
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10
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3
mutation records.
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NM_018182
Mutation details:
3
records
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