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 MRFAP1:
NM_001272053
Mutation details:
2
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NM_001272054
Mutation details:
2
records
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10
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2
mutation records.
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NM_033296
Mutation details:
2
records
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