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Mutation:
NPLOC4 I262T
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
Liver-HCC
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 260K
Affected site:
Position: 260
Residue: K
Type: ubiquitination
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 257K | YGRY[T/K]TEHKDIPLGIR | 3 |
distal
|
| 257M | YGRY[T/M]TEHKDIPLGIR | 3 |
distal
|
| 260I | YGRYTEH[K/I]KDIPLGIR | 0 |
direct
|
| 262T | YGRYTEHKD[I/T]IPLGIR | 2 |
proximal
|
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