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Summary

Isoform:
Position:
89
Ref:
S
Mutation:
F
PTM impact:
network-rewiring
PTM affected:
3
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

Hereditary cancer-predisposing syndrome, Ataxia-telangiectasia syndrome

Minor Allele Frequency: (ESP6500)

[0.0077]

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 83S

Affected site:

Position: 83
Residue: S
Type: phosphorylation

Impact:

distal

PTM Site: 85S

Affected site:

Position: 85
Residue: S
Type: phosphorylation

Impact:

distal

PTM Site: 86T

Affected site:

Position: 86
Residue: T
Type: phosphorylation

Only loss of PTM site:

CSNK1E (probability p=0.886)
Site: 86T (phosphorylation)
Position in motif: 3

External references

dbSNP:

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