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Mutation:
PPP1R12C P507L
Summary
Isoform:
Position:
507
Ref:
P
Mutation:
L
PTM impact:
proximal
PTM affected:
1
Kinases:
CDK2
Clinical Information
Cancer types: (TCGA MC3)
ESCA
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: 509S
Affected site:
Position: 509
Residue: S
Type: phosphorylation
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 514D | SRIPEPESPAKP[N/D]NVP | 5 |
distal
|
| 511V | SRIPEPESP[A/V]AKPNVP | 2 |
proximal
|
| 506D | SRIP[E/D]EPESPAKPNVP | 3 |
distal
|
| 505R | SRI[P/R]PEPESPAKPNVP | 4 |
distal
|
| 505S | SRI[P/S]PEPESPAKPNVP | 4 |
distal
|
| 505L | SRI[P/L]PEPESPAKPNVP | 4 |
distal
|
| 505A | SRI[P/A]PEPESPAKPNVP | 4 |
distal
|
| 507L | SRIPE[P/L]PESPAKPNVP | 2 |
proximal
|
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