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Mutation:
IL32 M11V
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.0154]
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 12K
Affected site:
Position: 12
Residue: K
Type: ubiquitination
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 6I | K[V/I]VLSDDMKKLKARMV | 6 |
distal
|
| 11V | KVLSDD[M/V]MKKLKARMV | 1 |
proximal
|
| 17Q | KVLSDDMKKLKA[R/Q]RMV | 5 |
distal
|
PTM Site: 13K
Affected site:
Position: 13
Residue: K
Type: ubiquitination
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 11V | VLSDD[M/V]MKKLKARMVM | 2 |
proximal
|
| 17Q | VLSDDMKKLKA[R/Q]RMVM | 4 |
distal
|
| 19A | VLSDDMKKLKARM[V/A]VM | 6 |
distal
|
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