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Mutation:
TDG G199S
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[7.1121]
Minor Allele Frequency: (1000 Genomes)
[10.1238]
PTM Site: 201K
Affected site:
Position: 201
Residue: K
Type: ubiquitination
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 199S | ERTTP[G/S]GSKDLSSKEF | 2 |
proximal
|
| 200I | ERTTPG[S/I]SKDLSSKEF | 1 |
proximal
|
| 197M | ERT[T/M]TPGSKDLSSKEF | 4 |
distal
|
PTM Site: 206K
Affected site:
Position: 206
Residue: K
Type: ubiquitination
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 200I | G[S/I]SKDLSSKEFREGGR | 6 |
distal
|
| 209C | GSKDLSSKEF[R/C]REGGR | 3 |
distal
|
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