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 FCAR:
 
NM_002000
Mutation details:
5
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NM_133269
Mutation details:
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NM_133272
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Mutation details:
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NM_133274
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Mutation details:
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NM_133277
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Mutation details:
2
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2
mutation records.
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NM_133278
Mutation details:
4
records
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4
mutation records.
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NM_133271
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Mutation details:
3
records
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10
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3
mutation records.
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NM_133273
No image for this transcript.
Mutation details:
3
records
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1
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10
/
3
mutation records.
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1
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1
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