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Mutation:
PPP1R12C P493L
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.0077]
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 499S
Affected site:
Position: 499
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 505R | PPCLENSSPPSRI[P/R]PE | 6 |
distal
|
| 505S | PPCLENSSPPSRI[P/S]PE | 6 |
distal
|
| 494Y | PP[C/Y]CLENSSPPSRIPE | 5 |
distal
|
| 493L | P[P/L]PCLENSSPPSRIPE | 6 |
distal
|
| 505L | PPCLENSSPPSRI[P/L]PE | 6 |
distal
|
| 505A | PPCLENSSPPSRI[P/A]PE | 6 |
distal
|
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