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Summary

Isoform:
Position:
29
Ref:
N
Mutation:
D
PTM impact:
distal
PTM affected:
2
Kinases:
CDK group, GSK-3 group, CDK7, ATM, GSK3B, MAPK14, MAPK12, CDK5, CDK9, PRKDC

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: 24K

Affected site:

Position: 24
Residue: K
Type: ubiquitination

Impact:

distal

PTM Site: 33S

Affected site:

Position: 33
Residue: S
Type: phosphorylation

Impact:

distal

External references

dbSNP:

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