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Mutation:
TP53 R282L
Summary
Isoform:
Position:
282
Ref:
R
Mutation:
L
PTM impact:
network-rewiring
PTM affected:
1
Kinases:
AURKB
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
Li-Fraumeni syndrome, 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
Only gain of PTM site:
STK11 (probability p=0.879)
Site: 284T (phosphorylation)
Position in motif: -2
Best loss of PTM site:
AURKB (probability p=0.893)
Site: 284T (phosphorylation)
Position in motif: -2
There are 2 other predicted
losses:
- ROCK1 (p=0.872)
- PRKACA (p=0.869)
Other known mutations affecting this site
External references
dbSNP:
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