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Mutation:
MINK1 R731L
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
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: 726S
Affected site:
Position: 726
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 731L | GHLPQAGSLERN[R/L]RVG | 5 |
distal
|
| 732M | GHLPQAGSLERNR[V/M]VG | 6 |
distal
|
| 731C | GHLPQAGSLERN[R/C]RVG | 5 |
distal
|
PTM Site: 735S
Affected site:
Position: 735
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 731L | ERN[R/L]RVGVSSKPDSSP | 4 |
distal
|
| 732M | ERNR[V/M]VGVSSKPDSSP | 3 |
distal
|
| 734A | ERNRVG[V/A]VSSKPDSSP | 1 |
proximal
|
| 738L | ERNRVGVSSK[P/L]PDSSP | 3 |
distal
|
| 731C | ERN[R/C]RVGVSSKPDSSP | 4 |
distal
|
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