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 AGL:
 
NM_000028
Mutation details:
15
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NM_000642
Mutation details:
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NM_000643
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_000644
Mutation details:
15
records
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1
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10
/
15
mutation records.
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1
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2
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NM_000645
No image for this transcript.
Mutation details:
15
records
Showing
1
-
10
/
15
mutation records.
Page
1
/
2
First
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Next
Last
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Download Data
NM_000646
No image for this transcript.
Mutation details:
15
records
Showing
1
-
10
/
15
mutation records.
Page
1
/
2
First
Prev
Next
Last
Jump to page
Download Data