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Mutation:
NOP2 I81M
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.0165]
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 82S
Affected site:
Position: 82
Residue: S
Type: phosphorylation
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 81M | GKLPKG[I/M]ISAGAVQTA | 1 |
proximal
|
PTM Site: 88T
Affected site:
Position: 88
Residue: T
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 90D | ISAGAVQTA[G/D]GKKGPQ | 2 |
proximal
|
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