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Mutation:
KRT79 N64K
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.0617]
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 61S
Affected site:
Position: 61
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
64K | TGGFGSRSLY[N/K]NLGGH | 3 |
distal
|
59R | TGGFG[S/R]SRSLYNLGGH | 2 |
network-rewiring
|
56S | TG[G/S]GFGSRSLYNLGGH | 5 |
distal
|
61N | TGGFGSR[S/N]SLYNLGGH | 0 |
direct
|
66R | TGGFGSRSLYNL[G/R]GGH | 5 |
distal
|
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