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 IRF3:
 
NM_001197122
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Mutation details:
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NM_001197123
Mutation details:
4
records
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4
mutation records.
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NM_001197125
Mutation details:
3
records
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mutation records.
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NM_001197126
Mutation details:
3
records
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3
mutation records.
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NM_001571
Mutation details:
5
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NM_001197124
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Mutation details:
3
records
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1
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10
/
3
mutation records.
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1
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NM_001197127
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Mutation details:
1
records
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10
/
1
mutation records.
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NM_001197128
No image for this transcript.
Mutation details:
1
records
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1
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10
/
1
mutation records.
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1
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