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Summary

Isoform:
Position:
11
Ref:
V
Mutation:
M
PTM impact:
distal
PTM affected:
2
Kinases:
CSNK2A1, CSNK2A1

Clinical Information

Cancer types: (TCGA MC3)

HNSC, COAD

Cancer types: (PCAWG)

Liver-HCC

Disease Annotations: (ClinVar)

Hereditary cancer-predisposing syndrome, Li-Fraumeni syndrome, Neoplasm of the breast

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 17S

Affected site:

Position: 17
Residue: S
Type: phosphorylation, O-glycosylation

Impact:

distal

PTM Site: 18T

Affected site:

Position: 18
Residue: T
Type: phosphorylation

Impact:

distal

External references

dbSNP:

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