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 ARPP21:
 
NM_001267617
Mutation details:
16
records
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10
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16
mutation records.
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NM_001267619
Mutation details:
16
records
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10
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16
mutation records.
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NM_016300
Mutation details:
16
records
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16
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NM_001025068
Mutation details:
3
records
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1
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10
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3
mutation records.
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NM_001025069
Mutation details:
3
records
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1
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10
/
3
mutation records.
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NM_001267616
Mutation details:
3
records
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1
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10
/
3
mutation records.
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NM_001267618
Mutation details:
3
records
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10
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3
mutation records.
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NM_198399
Mutation details:
3
records
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1
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10
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3
mutation records.
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