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Mutation:
CSDE1 S509T
Summary
Isoform:
Position:
509
Ref:
S
Mutation:
T
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: 503K
Affected site:
Position: 503
Residue: K
Type: ubiquitination
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 508V | TSPQIGDKVEFS[I/V]ISD | 5 |
distal
|
| 500M | TSPQ[I/M]IGDKVEFSISD | 3 |
distal
|
| 509T | TSPQIGDKVEFSI[S/T]SD | 6 |
distal
|
PTM Site: 511K
Affected site:
Position: 511
Residue: K
Type: ubiquitination
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 514L | VEFSISDKQR[P/L]PGQQV | 3 |
distal
|
| 508V | VEFS[I/V]ISDKQRPGQQV | 3 |
distal
|
| 509T | VEFSI[S/T]SDKQRPGQQV | 2 |
proximal
|
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