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 FIGNL1:
 
NM_001042762
Mutation details:
11
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NM_001287492
Mutation details:
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NM_001287493
Mutation details:
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NM_001287494
Mutation details:
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NM_001287495
Mutation details:
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NM_001287496
No image for this transcript.
Mutation details:
11
records
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1
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10
/
11
mutation records.
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NM_022116
Mutation details:
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