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Mutation:
AHR S81C
Summary
Clinical Information
Cancer types: (TCGA MC3)
STAD
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: 81S
Affected site:
Position: 81
Residue: S
Type: phosphorylation
Impact:
directOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 80R | VSYLRA[K/R]KSFFDVALK | 1 |
proximal
|
| 77M | VSY[L/M]LRAKSFFDVALK | 4 |
distal
|
| 81C | VSYLRAK[S/C]SFFDVALK | 0 |
direct
|
PTM Site: 88K
Affected site:
Position: 88
Residue: K
Type: ubiquitination
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 91T | SFFDVALKSS[P/T]PTERN | 3 |
distal
|
| 90F | SFFDVALKS[S/F]SPTERN | 2 |
proximal
|
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