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 ALG13:
 
NM_001099922
Mutation details:
18
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NM_001257230
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Mutation details:
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NM_001257231
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Mutation details:
17
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NM_001257234
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Mutation details:
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NM_001257237
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Mutation details:
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NM_001039210
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Mutation details:
3
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NM_001168385
Mutation details:
3
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NM_001257235
Mutation details:
2
records
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mutation records.
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NM_001257239
Mutation details:
2
records
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NM_001257240
Mutation details:
2
records
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2
mutation records.
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NM_001257241
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Mutation details:
2
records
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10
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2
mutation records.
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NM_018466
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Mutation details:
3
records
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3
mutation records.
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