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Mutation:
GMIP G429C
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
[0.0199681]
PTM Site: 425S
Affected site:
Position: 425
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
431Q | TPGSDVDSVGGGS[E/Q]ES | 6 |
distal
|
426M | TPGSDVDS[V/M]VGGGSES | 1 |
proximal
|
419L | T[P/L]PGSDVDSVGGGSES | 6 |
distal
|
429C | TPGSDVDSVGG[G/C]GSES | 4 |
distal
|
PTM Site: 430S
Affected site:
Position: 430
Residue: S
Type: phosphorylation
Impact:
proximalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
433W | VDSVGGGSES[R/W]RSLDS | 3 |
distal
|
432C | VDSVGGGSE[S/C]SRSLDS | 2 |
proximal
|
431Q | VDSVGGGS[E/Q]ESRSLDS | 1 |
proximal
|
426M | VDS[V/M]VGGGSESRSLDS | 4 |
distal
|
436N | VDSVGGGSESRSL[D/N]DS | 6 |
distal
|
429C | VDSVGG[G/C]GSESRSLDS | 1 |
proximal
|
PTM Site: 434S
Affected site:
Position: 434
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
Mutation | In sequence | Distance | Impact |
---|---|---|---|
433W | GGGSES[R/W]RSLDSPTSS | 1 |
proximal
|
432C | GGGSE[S/C]SRSLDSPTSS | 2 |
proximal
|
431Q | GGGS[E/Q]ESRSLDSPTSS | 3 |
distal
|
436N | GGGSESRSL[D/N]DSPTSS | 2 |
network-rewiring
|
429C | GG[G/C]GSESRSLDSPTSS | 5 |
distal
|
437A | GGGSESRSLD[S/A]SPTSS | 3 |
network-rewiring
|
440F | GGGSESRSLDSPT[S/F]SS | 6 |
distal
|
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