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 CYSLTR2:
 
NM_001308465
Mutation details:
3
records
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NM_001308467
Mutation details:
3
records
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NM_001308468
Mutation details:
3
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NM_001308469
Mutation details:
3
records
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10
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3
mutation records.
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NM_001308470
Mutation details:
3
records
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3
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NM_001308471
Mutation details:
3
records
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3
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NM_001308476
Mutation details:
3
records
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3
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NM_020377
Mutation details:
3
records
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1
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3
mutation records.
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