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Mutation:
COPA D188N
Summary
Clinical Information
Cancer types: (TCGA MC3)
LIHC
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 182R
Affected site:
Position: 182
Residue: R
Type: methylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
188V | GAVESDVRGITGV[D/V]DL | 6 |
distal
|
176V | G[A/V]AVESDVRGITGVDL | 6 |
distal
|
180H | GAVES[D/H]DVRGITGVDL | 2 |
proximal
|
188N | GAVESDVRGITGV[D/N]DL | 6 |
distal
|
PTM Site: 185T
Affected site:
Position: 185
Residue: T
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
188V | ESDVRGITGV[D/V]DLFGT | 3 |
distal
|
180H | ES[D/H]DVRGITGVDLFGT | 5 |
distal
|
188N | ESDVRGITGV[D/N]DLFGT | 3 |
distal
|
PTM Site: 193T
Affected site:
Position: 193
Residue: T
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
188V | GV[D/V]DLFGTTDAVVKHV | 5 |
distal
|
188N | GV[D/N]DLFGTTDAVVKHV | 5 |
distal
|
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