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Mutation:
TP53 Y61N
Summary
Isoform:
Position:
61
Ref:
Y
Mutation:
N
PTM impact:
direct
PTM affected:
3
Kinases:
AURKB,
AURKA,
PAK4,
AURORA A,
SRC
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
Liver-HCC
Disease Annotations: (ClinVar)
Hereditary cancer-predisposing syndrome
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 54R
Affected site:
Position: 54
Residue: R
Type: methylation
Impact:
distalOther known mutations affecting this site
PTM Site: 56S
Affected site:
Position: 56
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
PTM Site: 61Y
Affected site:
Position: 61
Residue: Y
Type: phosphorylation
Impact:
directOther known mutations affecting this site
External references
dbSNP:
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