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Mutation:
DNMT3A G298W
Summary
Clinical Information
Cancer types: (TCGA MC3)
UCEC
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
Inborn genetic diseases
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 299K
Affected site:
Position: 299
Residue: K
Type: ubiquitination
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 301W | IGELVWGKL[R/W]RGFSWW | 2 |
proximal
|
| 299Q | IGELVWG[K/Q]KLRGFSWW | 0 |
direct
|
| 298W | IGELVW[G/W]GKLRGFSWW | 1 |
proximal
|
| 302S | IGELVWGKLR[G/S]GFSWW | 3 |
distal
|
External references
dbSNP:
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