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Summary

Isoform:
Position:
209
Ref:
P
Mutation:
L
PTM impact:
network-rewiring
PTM affected:
1
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

Hereditary breast and ovarian cancer syndrome, Hereditary cancer-predisposing syndrome

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

[0.0199681]

PTM Site: 208T

Affected site:

Position: 208
Residue: T
Type: phosphorylation

Best loss of PTM site:

CDK1 (probability p=0.883)
Site: 208T (phosphorylation)
Position in motif: 1
There are 3 other predicted losses:
  • CDK2 (p=0.878)
  • GSK3B (p=0.871)
  • MAPK1 (p=0.855)

External references

dbSNP:

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