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Mutation:
AHR P91T
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
[0.0199681]
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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