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 IL1RAP:
 
NM_001167928
Mutation details:
14
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NM_001167929
Mutation details:
14
records
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10
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14
mutation records.
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NM_001167930
No image for this transcript.
Mutation details:
8
records
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1
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10
/
8
mutation records.
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NM_001167931
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Mutation details:
18
records
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10
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18
mutation records.
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NM_002182
Mutation details:
14
records
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14
mutation records.
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NM_134470
No image for this transcript.
Mutation details:
8
records
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1
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10
/
8
mutation records.
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1
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