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 SPOP:
 
NM_001007226
Mutation details:
14
records
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NM_001007227
Mutation details:
14
records
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14
mutation records.
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NM_001007228
Mutation details:
14
records
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1
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10
/
14
mutation records.
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2
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NM_001007229
Mutation details:
14
records
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1
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10
/
14
mutation records.
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2
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NM_001007230
Mutation details:
14
records
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14
mutation records.
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NM_003563
Mutation details:
14
records
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1
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10
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14
mutation records.
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