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 CDHR2:
NM_001171976
Mutation details:
22
records
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10
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22
mutation records.
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NM_017675
Mutation details:
22
records
Showing
1
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10
/
22
mutation records.
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1
/
3
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