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 SERPINA1:
 
NM_000295
Mutation details:
11
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NM_001002235
Mutation details:
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NM_001002236
Mutation details:
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NM_001127700
Mutation details:
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NM_001127701
Mutation details:
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NM_001127702
Mutation details:
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NM_001127703
Mutation details:
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NM_001127704
Mutation details:
11
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NM_001127705
Mutation details:
11
records
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11
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NM_001127706
Mutation details:
11
records
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10
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11
mutation records.
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NM_001127707
Mutation details:
11
records
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1
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10
/
11
mutation records.
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2
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