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Mutation:
HNRNPM G354S
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.1154]
Minor Allele Frequency: (1000 Genomes)
[0.09984029999999999]
PTM Site: 350R
Affected site:
Position: 350
Residue: R
Type: methylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 347S | RIGS[G/S]GVERMGAGMGF | 3 |
distal
|
| 354S | RIGSGVERMGA[G/S]GMGF | 4 |
distal
|
| 344V | R[I/V]IGSGVERMGAGMGF | 6 |
distal
|
| 351V | RIGSGVER[M/V]MGAGMGF | 1 |
proximal
|
| 350H | RIGSGVE[R/H]RMGAGMGF | 0 |
direct
|
PTM Site: 361R
Affected site:
Position: 361
Residue: R
Type: methylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 358S | GMGF[G/S]GLERMAAPIDR | 3 |
distal
|
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