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 VRK2:
 
NM_001130480
Mutation details:
8
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NM_001130481
Mutation details:
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NM_001130482
No image for this transcript.
Mutation details:
8
records
Showing
1
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10
/
8
mutation records.
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1
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1
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NM_001130483
No image for this transcript.
Mutation details:
7
records
Showing
1
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10
/
7
mutation records.
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1
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NM_001288836
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Mutation details:
7
records
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1
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10
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7
mutation records.
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NM_001288837
Mutation details:
8
records
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8
mutation records.
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NM_001288838
Mutation details:
7
records
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7
mutation records.
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NM_001288839
No image for this transcript.
Mutation details:
7
records
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1
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10
/
7
mutation records.
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1
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NM_006296
Mutation details:
8
records
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1
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10
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8
mutation records.
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