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 SLITRK2:
 
NM_001144003
Mutation details:
20
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20
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NM_001144004
Mutation details:
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NM_001144005
Mutation details:
20
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NM_001144006
Mutation details:
20
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20
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NM_001144008
Mutation details:
20
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10
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20
mutation records.
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NM_001144009
Mutation details:
20
records
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10
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20
mutation records.
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NM_001144010
Mutation details:
20
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20
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NM_032539
Mutation details:
20
records
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1
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10
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20
mutation records.
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