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Mutation:
MYEF2 L119I
Summary
Isoform:
Position:
119
Ref:
L
Mutation:
I
PTM impact:
proximal
PTM affected:
1
Kinases:
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: 117K
Affected site:
Position: 117
Residue: K
Type: ubiquitination
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 111I | D[M/I]MKWQAIKDLMREKV | 6 |
distal
|
| 119I | DMKWQAIKD[L/I]LMREKV | 2 |
proximal
|
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