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 RARB:
 
NM_000965
Mutation details:
3
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NM_001290216
Mutation details:
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NM_001290217
Mutation details:
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NM_001290266
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Mutation details:
3
records
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NM_001290276
Mutation details:
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NM_001290300
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Mutation details:
3
records
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3
mutation records.
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NM_016152
Mutation details:
3
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mutation records.
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NM_001290277
No image for this transcript.
Mutation details:
2
records
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1
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10
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2
mutation records.
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