You are viewing an updated version (2021) of the ActiveDriverDB. To view the previous version please visit activedriverdb.org/v2020
Mutation:
RAD51C L326S
Summary
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: 328K
Affected site:
Position: 328
Residue: K
Type: ubiquitination
Impact:
proximalOther known mutations affecting this site
Loading, please wait...
Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 328E | QRLATLY[K/E]KSPSQKEC | 0 |
direct
|
| 327C | QRLATL[Y/C]YKSPSQKEC | 1 |
proximal
|
| 329L | QRLATLYK[S/L]SPSQKEC | 1 |
proximal
|
| 326S | QRLAT[L/S]LYKSPSQKEC | 2 |
proximal
|
| 326W | QRLAT[L/W]LYKSPSQKEC | 2 |
proximal
|
External references
dbSNP:
If you have any questions or feedback about this mutation:
Contact us