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

Summary

Isoform:
Position:
510
Ref:
P
Mutation:
S
PTM impact:
network-rewiring
PTM affected:
2
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, Breast-ovarian cancer, familial 1

Minor Allele Frequency: (ESP6500)

[0.0538]

Minor Allele Frequency: (1000 Genomes)

[0.0399361]

PTM Site: 509S

Affected site:

Position: 509
Residue: S
Type: phosphorylation

Best loss of PTM site:

MAPK1 (probability p=0.956)
Site: 509S (phosphorylation)
Position in motif: 1
There are 5 other predicted losses:
  • MAPK3 (p=0.945)
  • MAPK8 (p=0.918)
  • MAPK14 (p=0.914)
  • CDK1 (p=0.896)
  • GSK3B (p=0.882)

PTM Site: 515T

External references

dbSNP:

If you have any questions or feedback about this mutation:

Contact us