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Mutation:
S100A13 S69W
Summary
Clinical Information
Cancer types: (TCGA MC3)
LUAD
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: 62S
Affected site:
Position: 62
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 66K | SLDEKMKSLDV[N/K]NQDS | 4 |
distal
|
| 64G | SLDEKMKSL[D/G]DVNQDS | 2 |
proximal
|
| 56F | S[L/F]LDEKMKSLDVNQDS | 6 |
distal
|
PTM Site: 69S
Affected site:
Position: 69
Residue: S
Type: phosphorylation
Impact:
directOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 74H | SLDVNQDSELKF[N/H]NEY | 5 |
distal
|
| 66K | SLDV[N/K]NQDSELKFNEY | 3 |
distal
|
| 64G | SL[D/G]DVNQDSELKFNEY | 5 |
distal
|
| 74S | SLDVNQDSELKF[N/S]NEY | 5 |
distal
|
| 69W | SLDVNQD[S/W]SELKFNEY | 0 |
direct
|
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