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Mutation:
TP53 P128T
Summary
Isoform:
Position:
128
Ref:
P
Mutation:
T
PTM impact:
proximal
PTM affected:
2
Kinases:
SRC
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
Hereditary cancer-predisposing syndrome, Li-Fraumeni syndrome
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 126Y
Affected site:
Position: 126
Residue: Y
Type: phosphorylation
Impact:
proximalOther known mutations affecting this site
PTM Site: 132K
Affected site:
Position: 132
Residue: K
Type: ubiquitination
Impact:
distalOther known mutations affecting this site
External references
dbSNP:
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