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Mutation:
TP53 C141Y
Summary
Clinical Information
Cancer types: (TCGA MC3)
LUSC, UCEC, BRCA, LGG, BLCA, STAD, HNSC
Cancer types: (PCAWG)
Panc-AdenoCA, Lymph-BNHL, Uterus-AdenoCA, Breast-AdenoCa
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: 139K
Affected site:
Position: 139
Residue: K
Type: ubiquitination
Impact:
proximalOther known mutations affecting this site
External references
dbSNP:
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