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Summary

Isoform:
Position:
292
Ref:
K
Mutation:
R
PTM impact:
direct
PTM affected:
3
Kinases:
EP300

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

Hereditary cancer-predisposing syndrome, Li-Fraumeni syndrome

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

External references

dbSNP:

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