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Summary

Isoform:
Position:
568
Ref:
G
Mutation:
C
PTM impact:
distal
PTM affected:
4
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

LUAD

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: 562R

Affected site:

Position: 562
Residue: R
Type: methylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
556L F[P/L]PPPGGDRGRGGPGG 6
distal
562C FPPPGGD[R/C]RGRGGPGG 0
direct
568C FPPPGGDRGRGGP[G/C]GG 6
distal
561N FPPPGG[D/N]DRGRGGPGG 1
proximal
564I FPPPGGDRG[R/I]RGGPGG 2
proximal
562L FPPPGGD[R/L]RGRGGPGG 0
direct

PTM Site: 564R

Affected site:

Position: 564
Residue: R
Type: methylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
562C PPGGD[R/C]RGRGGPGGMR 2
proximal
568C PPGGDRGRGGP[G/C]GGMR 4
distal
561N PPGG[D/N]DRGRGGPGGMR 3
distal
564I PPGGDRG[R/I]RGGPGGMR 0
direct
562L PPGGD[R/L]RGRGGPGGMR 2
proximal

PTM Site: 571R

Affected site:

Position: 571
Residue: R
Type: methylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
568C RGGP[G/C]GGMRGGRGGLM 3
distal
571W RGGPGGM[R/W]RGGRGGLM 0
direct

PTM Site: 574R

Affected site:

Position: 574
Residue: R
Type: methylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
580C PGGMRGGRGGLMD[R/C]RG 6
distal
568C P[G/C]GGMRGGRGGLMDRG 6
distal
571W PGGM[R/W]RGGRGGLMDRG 3
distal

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