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Mutation:
ZRANB3 P589L
Summary
Clinical Information
Cancer types: (TCGA MC3)
SKCM
Cancer types: (PCAWG)
Skin-Melanoma
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 588S
Affected site:
Position: 588
Residue: S
Type: phosphorylation
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 590L | AASEDHCSP[S/L]SEETPS | 2 |
proximal
|
| 585Y | AASE[D/Y]DHCSPSEETPS | 3 |
distal
|
| 583L | AA[S/L]SEDHCSPSEETPS | 5 |
distal
|
| 589L | AASEDHCS[P/L]PSEETPS | 1 |
proximal
|
| 593R | AASEDHCSPSEE[T/R]TPS | 5 |
distal
|
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