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Mutation:
RGPD3 N729D
Summary
Isoform:
Position:
729
Ref:
N
Mutation:
D
PTM impact:
proximal
PTM affected:
2
Kinases:
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
[0.0199681]
PTM Site: 731S
Affected site:
Position: 731
Residue: S
Type: phosphorylation
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 729D | DDSDS[N/D]NLSVVKKLPV | 2 |
proximal
|
| 725E | D[D/E]DSDSNLSVVKKLPV | 6 |
distal
|
PTM Site: 734K
Affected site:
Position: 734
Residue: K
Type: ubiquitination
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 729D | DS[N/D]NLSVVKKLPVPLE | 5 |
distal
|
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