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Mutation:
GGH E289Q
Summary
Clinical Information
Cancer types: (TCGA MC3)
LUSC
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: 287K
Affected site:
Position: 287
Residue: K
Type: ubiquitination
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 292V | RKNNHHFKSESE[E/V]EEK | 5 |
distal
|
| 289Q | RKNNHHFKS[E/Q]ESEEEK | 2 |
proximal
|
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