You are viewing an updated version (2021) of the ActiveDriverDB. To view the previous version please visit activedriverdb.org/v2020

Summary

Isoform:
Position:
79
Ref:
K
Mutation:
R
PTM impact:
direct
PTM affected:
5
Kinases:

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: 72T

Affected site:

Position: 72
Residue: T
Type: phosphorylation

Impact:

distal

PTM Site: 79K

Affected site:

Position: 79
Residue: K
Type: ubiquitination

Impact:

direct

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

Impact:

distal

External references

dbSNP:

If you have any questions or feedback about this mutation:

Contact us