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Mutation:
HNRNPM H329N
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.0154]
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 332S
Affected site:
Position: 332
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 329N | LGLD[H/N]HMASSIERMGQ | 3 |
distal
|
| 336P | LGLDHMASSIE[R/P]RMGQ | 4 |
distal
|
| 337I | LGLDHMASSIER[M/I]MGQ | 5 |
distal
|
PTM Site: 333S
Affected site:
Position: 333
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 329N | GLD[H/N]HMASSIERMGQT | 4 |
distal
|
| 336P | GLDHMASSIE[R/P]RMGQT | 3 |
distal
|
| 337I | GLDHMASSIER[M/I]MGQT | 4 |
distal
|
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