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Summary

Isoform:
Position:
9
Ref:
S
Mutation:
R
PTM impact:
direct
PTM affected:
3
Kinases:
CSNK1A1, CSNK1A1, ATM, CSNK1D, PRKDC, MAPK3, ATR, SMG1, NUAK1, MAPK1, STK11, CHEK2, CDK5, DNA-PK, TP53RK, PRKDC, CHEK1, BTK, ATM, MAPK14, DYRK1A

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

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:

distal

PTM Site: 9S

Affected site:

Position: 9
Residue: S
Type: phosphorylation

Impact:

direct

PTM Site: 15S

Affected site:

Position: 15
Residue: S
Type: phosphorylation

Impact:

distal

External references

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