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Mutation:
ARHGAP29 Q461K
Summary
Clinical Information
Cancer types: (TCGA MC3)
HNSC
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 463Y
Affected site:
Position: 463
Residue: Y
Type: phosphorylation
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 461R | LYDPG[Q/R]QEYSEFVKAT | 2 |
proximal
|
| 461E | LYDPG[Q/E]QEYSEFVKAT | 2 |
proximal
|
| 467F | LYDPGQEYSEF[V/F]VKAT | 4 |
distal
|
| 464R | LYDPGQEY[S/R]SEFVKAT | 1 |
proximal
|
| 461K | LYDPG[Q/K]QEYSEFVKAT | 2 |
proximal
|
PTM Site: 468K
Affected site:
Position: 468
Residue: K
Type: ubiquitination
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 467F | QEYSEF[V/F]VKATNSTEE | 1 |
proximal
|
| 464R | QEY[S/R]SEFVKATNSTEE | 4 |
distal
|
| 472L | QEYSEFVKATN[S/L]STEE | 4 |
distal
|
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