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 PARP9:
 
NM_001146102
Mutation details:
5
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NM_001146103
No image for this transcript.
Mutation details:
3
records
Showing
1
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10
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3
mutation records.
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1
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1
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NM_001146104
No image for this transcript.
Mutation details:
3
records
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1
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10
/
3
mutation records.
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NM_001146105
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Mutation details:
3
records
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10
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3
mutation records.
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NM_001146106
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Mutation details:
4
records
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10
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4
mutation records.
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NM_031458
Mutation details:
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