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Summary

Isoform:
Position:
74
Ref:
C
Mutation:
Y
PTM impact:
proximal
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)

no data

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 70K

Affected site:

Position: 70
Residue: K
Type: ubiquitination

Impact:

distal

PTM Site: 72T

Affected site:

Position: 72
Residue: T
Type: phosphorylation

Impact:

proximal

PTM Site: 79K

Affected site:

Position: 79
Residue: K
Type: ubiquitination

Impact:

distal

External references

dbSNP:

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