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Mutation:
PRKG2 M14I
Summary
Clinical Information
Cancer types: (TCGA MC3)
UCEC
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 11S
Affected site:
Position: 11
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 9T | WKLSK[A/T]ALSLEMIQLK | 2 |
proximal
|
| 11F | WKLSKAL[S/F]SLEMIQLK | 0 |
direct
|
| 13K | WKLSKALSL[E/K]EMIQLK | 2 |
proximal
|
| 14I | WKLSKALSLE[M/I]MIQLK | 3 |
distal
|
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