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Mutation:
WIPF1 G426R
Summary
Clinical Information
Cancer types: (TCGA MC3)
HNSC
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 422R
Affected site:
Position: 422
Residue: R
Type: methylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 418V | RPP[L/V]LPPDRPSAGAPP | 4 |
distal
|
| 426R | RPPLPPDRPSA[G/R]GAPP | 4 |
distal
|
| 420H | RPPLP[P/H]PDRPSAGAPP | 2 |
proximal
|
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