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Mutation:
ARHGAP29 S472L
Summary
Clinical Information
Cancer types: (TCGA MC3)
BLCA
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: 468K
Affected site:
Position: 468
Residue: K
Type: ubiquitination
Impact:
distalOther known mutations affecting this site
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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
|
Showing 1 to 3 of 3 rows
PTM Site: 477K
Affected site:
Position: 477
Residue: K
Type: ubiquitination
Impact:
distalOther known mutations affecting this site
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Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 476Q | TNSTEE[E/Q]EKVDGNVNK | 1 |
proximal
|
| 479H | TNSTEEEKV[D/H]DGNVNK | 2 |
proximal
|
| 472L | TN[S/L]STEEEKVDGNVNK | 5 |
distal
|
Showing 1 to 3 of 3 rows
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