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 PDE9A:
 
NM_001001567
Mutation details:
8
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NM_001001568
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Mutation details:
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NM_001001569
Mutation details:
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NM_001001570
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Mutation details:
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NM_001001571
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Mutation details:
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NM_001001572
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Mutation details:
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NM_001001573
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Mutation details:
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mutation records.
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NM_001001574
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Mutation details:
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7
mutation records.
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NM_001001575
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Mutation details:
7
records
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10
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7
mutation records.
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NM_001001576
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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_001001577
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Mutation details:
8
records
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10
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8
mutation records.
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NM_001001578
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Mutation details:
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8
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NM_001001579
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Mutation details:
7
records
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10
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7
mutation records.
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NM_001001580
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Mutation details:
7
records
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10
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7
mutation records.
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NM_001001581
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Mutation details:
9
records
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10
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9
mutation records.
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NM_001001582
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Mutation details:
10
records
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10
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10
mutation records.
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NM_001001583
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Mutation details:
9
records
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10
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9
mutation records.
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NM_001001584
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Mutation details:
7
records
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10
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7
mutation records.
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NM_001001585
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Mutation details:
7
records
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10
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7
mutation records.
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NM_001315533
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Mutation details:
7
records
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7
mutation records.
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NM_002606
Mutation details:
10
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