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Mutation:
TP53 P20R
Summary
Isoform:
Position:
20
Ref:
P
Mutation:
R
PTM impact:
network-rewiring
PTM affected:
3
Kinases:
CSNK2A1,
CSNK2A1,
CSNK2A1
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
Hereditary cancer-predisposing syndrome
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 17S
Affected site:
Position: 17
Residue: S
Type: phosphorylation, O-glycosylation
Impact:
distalOther known mutations affecting this site
PTM Site: 18T
Affected site:
Position: 18
Residue: T
Type: phosphorylation
Best gain of PTM site:
AKT1 (probability p=0.964)
Site: 23T (phosphorylation)
Position in motif: -3
There are 3 other predicted
gains:
- PRKACA (p=0.887)
- PRKCB (p=0.878)
- PRKAA1 (p=0.877)
Other known mutations affecting this site
PTM Site: 23T
Affected site:
Position: 23
Residue: T
Type: phosphorylation
Best gain of PTM site:
AKT1 (probability p=0.964)
Site: 23T (phosphorylation)
Position in motif: -3
There are 3 other predicted
gains:
- PRKACA (p=0.887)
- PRKCB (p=0.878)
- PRKAA1 (p=0.877)
Other known mutations affecting this site
External references
dbSNP:
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