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Mutation:
NOP2 L97I
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.0082]
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 96S
Affected site:
Position: 96
Residue: S
Type: phosphorylation
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 102Q | AGKKGPQSLFNAP[R/Q]RG | 6 |
distal
|
| 97I | AGKKGPQS[L/I]LFNAPRG | 1 |
proximal
|
| 90D | A[G/D]GKKGPQSLFNAPRG | 6 |
distal
|
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