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Summary

Isoform:
Position:
35
Ref:
L
Mutation:
M
PTM impact:
proximal
PTM affected:
2
Kinases:
CDK group, GSK-3 group, CDK5, PRKDC, GSK3B, CDK7, MAPK12, MAPK14, CDK9, ATM, ATR, CHEK2, PRKDC, MAPKAPK5, DNA-PK, CHEK1, ATM, CSNK1A1

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: 33S

Affected site:

Position: 33
Residue: S
Type: phosphorylation

Impact:

proximal

PTM Site: 37S

Affected site:

Position: 37
Residue: S
Type: phosphorylation

Impact:

proximal

External references

dbSNP:

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