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 UTY:
 
NM_001258249
Mutation details:
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NM_001258250
Mutation details:
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NM_001258251
Mutation details:
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NM_001258252
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Mutation details:
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NM_001258253
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Mutation details:
5
records
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10
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5
mutation records.
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NM_001258254
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Mutation details:
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records
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4
mutation records.
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NM_001258255
Mutation details:
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NM_001258256
Mutation details:
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NM_001258257
Mutation details:
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NM_001258258
Mutation details:
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NM_001258259
Mutation details:
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NM_001258260
Mutation details:
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NM_001258261
Mutation details:
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NM_001258262
Mutation details:
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NM_001258263
Mutation details:
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NM_001258264
Mutation details:
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NM_001258265
Mutation details:
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NM_001258266
Mutation details:
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NM_001258267
Mutation details:
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records
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NM_001258268
Mutation details:
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NM_001258269
Mutation details:
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NM_001258270
Mutation details:
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NM_007125
Mutation details:
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NM_182659
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Mutation details:
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NM_182660
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Mutation details:
1
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1
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