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

Summary

Isoform:
Position:
214
Ref:
D
Mutation:
N
PTM impact:
distal
PTM affected:
2
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

Hereditary breast and ovarian cancer syndrome, Hereditary cancer-predisposing syndrome

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 208T

Affected site:

Position: 208
Residue: T
Type: phosphorylation

Impact:

distal

PTM Site: 220S

Affected site:

Position: 220
Residue: S
Type: phosphorylation

Impact:

distal

External references

dbSNP:

If you have any questions or feedback about this mutation:

Contact us