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Mutation:
ZRANB3 D566N
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.0083]
Minor Allele Frequency: (1000 Genomes)
[0.0798722]
PTM Site: 569S
Affected site:
Position: 569
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
575M | RDIIDYESDVEPE[T/M]TK | 6 |
distal
|
573S | RDIIDYESDVE[P/S]PETK | 4 |
distal
|
566N | RDII[D/N]DYESDVEPETK | 3 |
distal
|
564S | RD[I/S]IIDYESDVEPETK | 5 |
distal
|
563G | R[D/G]DIIDYESDVEPETK | 6 |
distal
|
574K | RDIIDYESDVEP[E/K]ETK | 5 |
distal
|
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