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 FAM107B:
 
NM_001282695
Mutation details:
2
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NM_001282696
Mutation details:
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NM_001282697
Mutation details:
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NM_001282698
Mutation details:
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NM_001282699
Mutation details:
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NM_001282700
Mutation details:
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NM_001282701
Mutation details:
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NM_001282702
Mutation details:
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NM_001282703
Mutation details:
2
records
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2
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NM_031453
No image for this transcript.
Mutation details:
6
records
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6
mutation records.
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