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Mutation:
LRBA S2198L
Summary
Clinical Information
Cancer types: (TCGA MC3)
SKCM
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 2198S
Affected site:
Position: 2198
Residue: S
Type: phosphorylation
Impact:
directOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 2203H | LPQTRRISLASP[R/H]RQL | 5 |
distal
|
| 2203C | LPQTRRISLASP[R/C]RQL | 5 |
distal
|
| 2196H | LPQTR[R/H]RISLASPRQL | 2 |
network-rewiring
|
| 2198L | LPQTRRI[S/L]SLASPRQL | 0 |
direct
|
PTM Site: 2201S
Affected site:
Position: 2201
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 2203H | TRRISLASP[R/H]RQLFKA | 2 |
network-rewiring
|
| 2203C | TRRISLASP[R/C]RQLFKA | 2 |
network-rewiring
|
| 2196H | TR[R/H]RISLASPRQLFKA | 5 |
network-rewiring
|
| 2198L | TRRI[S/L]SLASPRQLFKA | 3 |
distal
|
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