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Mutation:
VRTN S265T
Summary
Clinical Information
Cancer types: (TCGA MC3)
KIRP
Cancer types: (PCAWG)
Kidney-RCC
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 265S
Affected site:
Position: 265
Residue: S
Type: phosphorylation
Impact:
directOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 263T | LPALA[P/T]PLSSPAKTLE | 2 |
proximal
|
| 265T | LPALAPL[S/T]SSPAKTLE | 0 |
direct
|
PTM Site: 266S
Affected site:
Position: 266
Residue: S
Type: phosphorylation
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 263T | PALA[P/T]PLSSPAKTLEL | 3 |
distal
|
| 265T | PALAPL[S/T]SSPAKTLEL | 1 |
proximal
|
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