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Mutation:
TP53 K139N
Summary
Clinical Information
Cancer types: (TCGA MC3)
BLCA, LIHC
Cancer types: (PCAWG)
Lymph-BNHL
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 132K
Affected site:
Position: 132
Residue: K
Type: ubiquitination
Impact:
distalOther known mutations affecting this site
PTM Site: 139K
Affected site:
Position: 139
Residue: K
Type: ubiquitination
Impact:
directOther known mutations affecting this site
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