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Mutation:
MSH6 A36V
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)
[0.0086]
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 33R
Affected site:
Position: 33
Residue: R
Type: methylation
Impact:
distalOther known mutations affecting this site
PTM Site: 41S
Affected site:
Position: 41
Residue: S
Type: phosphorylation, phosphorylation (SARS-CoV-2)
Impact:
distalOther known mutations affecting this site
PTM Site: 43S
Affected site:
Position: 43
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
External references
dbSNP:
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