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Summary

Isoform:
Position:
8
Ref:
P
Mutation:
T
PTM impact:
proximal
PTM affected:
3
Kinases:
CSNK1A1, ATM, CSNK1A1, PRKDC, CSNK1D, DYRK1A, SMG1, DNA-PK, PRKDC, MAPK1, CHEK1, MAPK14, ATR, CHEK2, ATM, MAPK3, BTK, STK11, TP53RK, NUAK1, CDK5

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: 6S

Affected site:

Position: 6
Residue: S
Type: phosphorylation

Impact:

proximal

PTM Site: 9S

Affected site:

Position: 9
Residue: S
Type: phosphorylation

Impact:

proximal

PTM Site: 15S

Affected site:

Position: 15
Residue: S
Type: phosphorylation

Impact:

distal

External references

dbSNP:

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