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Mutation:
EXOSC2 R11G
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
Prost-AdenoCA
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 15S
Affected site:
Position: 15
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
15R | PVARKPL[S/R]SERLGRDT | 0 |
direct
|
20C | PVARKPLSERLG[R/C]RDT | 5 |
distal
|
11G | PVA[R/G]RKPLSERLGRDT | 4 |
distal
|
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