Summary

Isoform:
Position:
293
Ref:
G
Mutation:
R
PTM impact:
proximal
PTM affected:
2
Kinases:
EP300

Clinical Information

Cancer types: (TCGA MC3)

no data

Disease Annotations: (ClinVar)

Hereditary cancer-predisposing syndrome, Tumor predisposition syndrome

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 292K

Affected site:

Position: 292
Residue: K
Type: acetylation,ubiquitination

Impact:

proximal

PTM Site: 291K

External references

dbSNP:

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