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Mutation:
TP53 G279E
Summary
Isoform:
Position:
279
Ref:
G
Mutation:
E
PTM impact:
distal
PTM affected:
1
Kinases:
AURKB
Clinical Information
Cancer types: (TCGA MC3)
LUSC, UCEC, PRAD, LGG
Cancer types: (PCAWG)
Liver-HCC, Prost-AdenoCA
Disease Annotations: (ClinVar)
Hereditary cancer-predisposing syndrome
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 284T
Affected site:
Position: 284
Residue: T
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
External references
dbSNP:
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