You are viewing an updated version (2021) of the ActiveDriverDB. To view the previous version please visit activedriverdb.org/v2020

Summary

Isoform:
Position:
174
Ref:
Q
Mutation:
H
PTM impact:
proximal
PTM affected:
5
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

KIRP

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: 167S

Affected site:

Position: 167
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
166Y TPLPTI[S/Y]SSSAENTRQ 1
proximal
166C TPLPTI[S/C]SSSAENTRQ 1
proximal
170Q TPLPTISSSA[E/Q]ENTRQ 3
network-rewiring

PTM Site: 168S

Affected site:

Position: 168
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
166Y PLPTI[S/Y]SSSAENTRQN 2
proximal
166C PLPTI[S/C]SSSAENTRQN 2
proximal
170Q PLPTISSSA[E/Q]ENTRQN 2
proximal
174H PLPTISSSAENTR[Q/H]QN 6
distal

PTM Site: 172T

Affected site:

Position: 172
Residue: T
Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation In sequence Distance Impact
166Y I[S/Y]SSSAENTRQNGSND 6
distal
166C I[S/C]SSSAENTRQNGSND 6
distal
177G ISSSAENTRQNG[S/G]SND 5
distal
170Q ISSSA[E/Q]ENTRQNGSND 2
network-rewiring
174H ISSSAENTR[Q/H]QNGSND 2
proximal

PTM Site: 177S

Affected site:

Position: 177
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
177G ENTRQNG[S/G]SNDSDRYS 0
direct
174H ENTR[Q/H]QNGSNDSDRYS 3
distal

PTM Site: 180S

Affected site:

Position: 180
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
177G RQNG[S/G]SNDSDRYSDNE 3
distal
186S RQNGSNDSDRYSD[N/S]NE 6
distal
185H RQNGSNDSDRYS[D/H]DNE 5
distal
174H R[Q/H]QNGSNDSDRYSDNE 6
distal

If you have any questions or feedback about this mutation:

Contact us