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 BLCAP:
 
NM_001167820
Mutation details:
2
records
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mutation records.
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NM_001167821
Mutation details:
2
records
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NM_001167822
Mutation details:
2
records
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NM_001167823
Mutation details:
2
records
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2
mutation records.
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NM_001317074
Mutation details:
2
records
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NM_001317075
Mutation details:
2
records
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10
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2
mutation records.
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NM_006698
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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