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Mutation:
LSM14A R406C
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.0077]
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 409Y
Affected site:
Position: 409
Residue: Y
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 406C | PNRG[R/C]RGGYRGRGGLG | 3 |
distal
|
| 404C | PN[R/C]RGRGGYRGRGGLG | 5 |
distal
|
| 410K | PNRGRGGY[R/K]RGRGGLG | 1 |
proximal
|
| 404L | PN[R/L]RGRGGYRGRGGLG | 5 |
distal
|
| 415I | PNRGRGGYRGRGG[L/I]LG | 6 |
distal
|
PTM Site: 412R
Affected site:
Position: 412
Residue: R
Type: methylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 406C | G[R/C]RGGYRGRGGLGFRG | 6 |
distal
|
| 410K | GRGGY[R/K]RGRGGLGFRG | 2 |
proximal
|
| 415I | GRGGYRGRGG[L/I]LGFRG | 3 |
distal
|
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