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Summary

Isoform:
Position:
74
Ref:
S
Mutation:
G
PTM impact:
direct
PTM affected:
3
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

Bloom syndrome

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 68T

Affected site:

Position: 68
Residue: T
Type: phosphorylation

Impact:

distal

PTM Site: 72S

Affected site:

Position: 72
Residue: S
Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation In sequence Distance Impact
67I VN[V/I]VTEDFSFSEPLPN 5
distal
67D VN[V/D]VTEDFSFSEPLPN 5
distal
69K VNVT[E/K]EDFSFSEPLPN 3
distal
70N VNVTE[D/N]DFSFSEPLPN 2
proximal
72A VNVTEDF[S/A]SFSEPLPN 0
direct
74G VNVTEDFSF[S/G]SEPLPN 2
proximal
76T VNVTEDFSFSE[P/T]PLPN 4
distal
76S VNVTEDFSFSE[P/S]PLPN 4
distal
77V VNVTEDFSFSEP[L/V]LPN 5
distal
68N VNV[T/N]TEDFSFSEPLPN 4
distal
75K VNVTEDFSFS[E/K]EPLPN 3
network-rewiring

PTM Site: 74S

Affected site:

Position: 74
Residue: S
Type: phosphorylation

Impact:

direct

Other known mutations affecting this site

Mutation In sequence Distance Impact
69K VT[E/K]EDFSFSEPLPNTT 5
distal
70N VTE[D/N]DFSFSEPLPNTT 4
distal
72A VTEDF[S/A]SFSEPLPNTT 2
proximal
74G VTEDFSF[S/G]SEPLPNTT 0
direct
76T VTEDFSFSE[P/T]PLPNTT 2
proximal
76S VTEDFSFSE[P/S]PLPNTT 2
proximal
77V VTEDFSFSEP[L/V]LPNTT 3
distal
80A VTEDFSFSEPLPN[T/A]TT 6
distal
68N V[T/N]TEDFSFSEPLPNTT 6
distal
75K VTEDFSFS[E/K]EPLPNTT 1
proximal

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