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Mutation:
GLIPR2 L31I
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.0384]
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 30K
Affected site:
Position: 30
Residue: K
Type: ubiquitination
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 26I | KHG[V/I]VPPLKLCKNLNR | 4 |
distal
|
| 31I | KHGVPPLK[L/I]LCKNLNR | 1 |
proximal
|
| 33E | KHGVPPLKLC[K/E]KNLNR | 3 |
distal
|
PTM Site: 33K
Affected site:
Position: 33
Residue: K
Type: ubiquitination
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 31I | VPPLK[L/I]LCKNLNREAQ | 2 |
proximal
|
| 38K | VPPLKLCKNLNR[E/K]EAQ | 5 |
distal
|
| 39S | VPPLKLCKNLNRE[A/S]AQ | 6 |
distal
|
| 33E | VPPLKLC[K/E]KNLNREAQ | 0 |
direct
|
| 37W | VPPLKLCKNLN[R/W]REAQ | 4 |
distal
|
| 37Q | VPPLKLCKNLN[R/Q]REAQ | 4 |
distal
|
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