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Mutation:
TP53 L47S
Summary
Isoform:
Position:
47
Ref:
L
Mutation:
S
PTM impact:
distal
PTM affected:
3
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: 50R
Affected site:
Position: 50
Residue: R
Type: methylation
Impact:
distalOther known mutations affecting this site
PTM Site: 52T
Affected site:
Position: 52
Residue: T
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
PTM Site: 54R
Affected site:
Position: 54
Residue: R
Type: methylation
Impact:
distalOther known mutations affecting this site
External references
dbSNP:
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