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Mutation:
PPP1R12C A511V
Summary
Isoform:
Position:
511
Ref:
A
Mutation:
V
PTM impact:
proximal
PTM affected:
1
Kinases:
CDK2
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: 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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