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Summary

Isoform:
Position:
125
Ref:
R
Mutation:
Q
PTM impact:
direct
PTM affected:
3
Kinases:
MAPK7

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: 121K

Affected site:

Position: 121
Residue: K
Type: ubiquitination

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
125Q ERNIHGLKVNT[R/Q]RAGP 4
distal
115W E[R/W]RNIHGLKVNTRAGP 6
distal
118R ERNI[H/R]HGLKVNTRAGP 3
distal
126S ERNIHGLKVNTR[A/S]AGP 5
distal
127V ERNIHGLKVNTRA[G/V]GP 6
distal

PTM Site: 125R

Affected site:

Position: 125
Residue: R
Type: methylation

Impact:

direct

Other known mutations affecting this site

Mutation In sequence Distance Impact
125Q HGLKVNT[R/Q]RAGPSQHS 0
direct
128S HGLKVNTRAG[P/S]PSQHS 3
distal
131Y HGLKVNTRAGPSQ[H/Y]HS 6
distal
126S HGLKVNTR[A/S]AGPSQHS 1
proximal
127V HGLKVNTRA[G/V]GPSQHS 2
proximal

PTM Site: 129S

Affected site:

Position: 129
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
125Q VNT[R/Q]RAGPSQHSSPAV 4
distal
134L VNTRAGPSQHSS[P/L]PAV 5
distal
128S VNTRAG[P/S]PSQHSSPAV 1
proximal
131Y VNTRAGPSQ[H/Y]HSSPAV 2
proximal
126S VNTR[A/S]AGPSQHSSPAV 3
network-rewiring
127V VNTRA[G/V]GPSQHSSPAV 2
proximal

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