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 SH2B1:
 
NM_001145795
Mutation details:
16
records
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10
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16
mutation records.
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NM_001145796
Mutation details:
15
records
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NM_001145797
Mutation details:
15
records
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NM_001145812
Mutation details:
15
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15
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NM_001308293
Mutation details:
16
records
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1
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10
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16
mutation records.
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NM_015503
Mutation details:
15
records
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1
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10
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15
mutation records.
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NM_001308294
Mutation details:
4
records
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10
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4
mutation records.
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