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 MID1:
 
NM_000381
Mutation details:
8
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NM_001098624
Mutation details:
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NM_001193277
Mutation details:
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NM_001193278
Mutation details:
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NM_001193279
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Mutation details:
3
records
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3
mutation records.
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NM_001193280
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Mutation details:
3
records
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3
mutation records.
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NM_033289
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Mutation details:
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NM_033290
Mutation details:
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NM_001193281
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Mutation details:
1
records
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10
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1
mutation records.
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