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Mutation:
EWSR1 R562C
Summary
Clinical Information
Cancer types: (TCGA MC3)
BLCA
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: 562R
Affected site:
Position: 562
Residue: R
Type: methylation
Impact:
directOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 556L | F[P/L]PPPGGDRGRGGPGG | 6 |
distal
|
| 562C | FPPPGGD[R/C]RGRGGPGG | 0 |
direct
|
| 568C | FPPPGGDRGRGGP[G/C]GG | 6 |
distal
|
| 561N | FPPPGG[D/N]DRGRGGPGG | 1 |
proximal
|
| 564I | FPPPGGDRG[R/I]RGGPGG | 2 |
proximal
|
| 562L | FPPPGGD[R/L]RGRGGPGG | 0 |
direct
|
PTM Site: 564R
Affected site:
Position: 564
Residue: R
Type: methylation
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 562C | PPGGD[R/C]RGRGGPGGMR | 2 |
proximal
|
| 568C | PPGGDRGRGGP[G/C]GGMR | 4 |
distal
|
| 561N | PPGG[D/N]DRGRGGPGGMR | 3 |
distal
|
| 564I | PPGGDRG[R/I]RGGPGGMR | 0 |
direct
|
| 562L | PPGGD[R/L]RGRGGPGGMR | 2 |
proximal
|
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