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Summary

Isoform:
Position:
70
Ref:
A
Mutation:
P
PTM impact:
proximal
PTM affected:
1
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

MYH-associated polyposis, Hereditary cancer-predisposing syndrome

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 72K

Affected site:

Position: 72
Residue: K
Type: ubiquitination

Impact:

proximal

External references

dbSNP:

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