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 NTRK2:
 
NM_001007097
Mutation details:
8
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NM_001018064
Mutation details:
11
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NM_001018065
No image for this transcript.
Mutation details:
10
records
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1
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10
/
10
mutation records.
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NM_001018066
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Mutation details:
9
records
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10
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9
mutation records.
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NM_001291937
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Mutation details:
8
records
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10
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8
mutation records.
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NM_006180
Mutation details:
12
records
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