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Mutation:
MINK1 V769M
Summary
Clinical Information
Cancer types: (TCGA MC3)
STAD
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.0081]
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 763S
Affected site:
Position: 763
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 768L | GHLPQAGSLERN[R/L]RVG | 5 |
distal
|
| 769M | GHLPQAGSLERNR[V/M]VG | 6 |
distal
|
| 768C | GHLPQAGSLERN[R/C]RVG | 5 |
distal
|
PTM Site: 772S
Affected site:
Position: 772
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 768L | ERN[R/L]RVGVSSKPDSSP | 4 |
distal
|
| 769M | ERNR[V/M]VGVSSKPDSSP | 3 |
distal
|
| 771A | ERNRVG[V/A]VSSKPDSSP | 1 |
proximal
|
| 775L | ERNRVGVSSK[P/L]PDSSP | 3 |
distal
|
| 768C | ERN[R/C]RVGVSSKPDSSP | 4 |
distal
|
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