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Summary

Isoform:
Position:
101
Ref:
K
Mutation:
N
PTM impact:
direct
PTM affected:
3
Kinases:
AURKA

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

Li-Fraumeni syndrome, Hereditary cancer-predisposing syndrome

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 99S

Affected site:

Position: 99
Residue: S
Type: phosphorylation

Best loss of PTM site:

PRKCA (probability p=0.926)
Site: 99S (phosphorylation)
Position in motif: 2
There are 2 other predicted losses:
  • PRKCB (p=0.895)
  • PRKCG (p=0.857)

External references

dbSNP:

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