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Mutation:
MSH6 S63Y
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
Hereditary nonpolyposis colorectal neoplasms, Hereditary cancer-predisposing syndrome
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 63S
Affected site:
Position: 63
Residue: S
Type: phosphorylation
Impact:
directOther known mutations affecting this site
PTM Site: 65S
Affected site:
Position: 65
Residue: S
Type: phosphorylation, phosphorylation (SARS-CoV-2)
Impact:
proximalOther known mutations affecting this site
PTM Site: 70K
Affected site:
Position: 70
Residue: K
Type: acetylation
Impact:
distalOther known mutations affecting this site
External references
dbSNP:
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