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Mutation:
TRIM29 D39N
Summary
Clinical Information
Cancer types: (TCGA MC3)
SARC
Cancer types: (PCAWG)
Bone-Leiomyo
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 33T
Affected site:
Position: 33
Residue: T
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 30K | SGSL[E/K]ENGTKADGKDA | 3 |
network-rewiring
|
| 39N | SGSLENGTKADGK[D/N]DA | 6 |
distal
|
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