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Mutation:
HPSE2 G191C
Summary
Isoform:
Position:
191
Ref:
G
Mutation:
C
PTM impact:
proximal
PTM affected:
2
Kinases:
Clinical Information
Cancer types: (TCGA MC3)
STAD
Cancer types: (PCAWG)
Stomach-AdenoCA
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 188S
Affected site:
Position: 188
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 187T | IRIYSR[A/T]ASLYGPNIG | 1 |
proximal
|
| 182W | I[R/W]RIYSRASLYGPNIG | 6 |
distal
|
| 191C | IRIYSRASLY[G/C]GPNIG | 3 |
distal
|
| 186T | IRIYS[R/T]RASLYGPNIG | 2 |
network-rewiring
|
| 189V | IRIYSRAS[L/V]LYGPNIG | 1 |
proximal
|
PTM Site: 190Y
Affected site:
Position: 190
Residue: Y
Type: phosphorylation
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 187T | IYSR[A/T]ASLYGPNIGRP | 3 |
distal
|
| 191C | IYSRASLY[G/C]GPNIGRP | 1 |
proximal
|
| 186T | IYS[R/T]RASLYGPNIGRP | 4 |
distal
|
| 189V | IYSRAS[L/V]LYGPNIGRP | 1 |
proximal
|
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