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Mutation:
SCO2 K18N
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
Breast-AdenoCa
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 15S
Affected site:
Position: 15
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 20P | PTAWHRLSQLKP[R/P]RVL | 5 |
distal
|
| 18N | PTAWHRLSQL[K/N]KPRVL | 3 |
distal
|
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