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 ARHGAP22:
 
NM_001256024
Mutation details:
12
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NM_001256025
No image for this transcript.
Mutation details:
12
records
Showing
1
-
10
/
12
mutation records.
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1
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2
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NM_001256026
No image for this transcript.
Mutation details:
10
records
Showing
1
-
10
/
10
mutation records.
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1
/
1
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NM_021226
Mutation details:
12
records
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1
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10
/
12
mutation records.
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2
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