After several years of serving the research community, our ActiveDriverDB database will be retired on May 1st 2026. Please make sure to download any data you need and update your links or workflows before that date.

We want to sincerely thank all our users for their support, feedback, and collaboration over the years — your contributions have been invaluable to this project. A special thank you to Dr. Michal Krassowski for leading the development of our open-source software and database.

For any questions or assistance, please contact Jüri Reimand (juri.reimand@utoronto.ca).

You are viewing an updated version (2021) of the ActiveDriverDB. To view the previous version please visit activedriverdb.org/v2020

Summary

Isoform:
Position:
316
Ref:
P
Mutation:
S
PTM impact:
network-rewiring
PTM affected:
7
Kinases:
AURORA A, CDK9, CDK2, CDK5, NEK2, CDK1, AURKA, KAT2B

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

PTM Site: 312T

PTM Site: 313S

Affected site:

Position: 313
Residue: S
Type: phosphorylation

Impact:

distal

PTM Site: 314S

PTM Site: 315S

Affected site:

Position: 315
Residue: S
Type: phosphorylation

Best loss of PTM site:

MAPK1 (probability p=0.956)
Site: 315S (phosphorylation)
Position in motif: 1
There are 8 other predicted losses:
  • MAPK3 (p=0.954)
  • CDK5 (p=0.952)
  • MAPK14 (p=0.91)
  • CDK1 (p=0.907)
  • MTOR (p=0.896)
  • MAPK9 (p=0.876)
  • GSK3B (p=0.864)
  • CDK4 (p=0.851)

PTM Site: 319K

PTM Site: 320K

PTM Site: 321K

Affected site:

Position: 321
Residue: K
Type: ubiquitination, acetylation

Impact:

distal

External references

dbSNP:

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