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Summary

Isoform:
Position:
742
Ref:
R
Mutation:
Q
PTM impact:
proximal
PTM affected:
3
Kinases:
SRC, SRC, SRC

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: 736Y

Affected site:

Position: 736
Residue: Y
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
740C FGMSRNLYSGD[Y/C]YYRI 4
distal
737R FGMSRNLY[S/R]SGDYYRI 1
proximal
742W FGMSRNLYSGDYY[R/W]RI 6
distal
742Q FGMSRNLYSGDYY[R/Q]RI 6
distal

PTM Site: 740Y

Affected site:

Position: 740
Residue: Y
Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation In sequence Distance Impact
740C RNLYSGD[Y/C]YYRIQGRA 0
direct
746Q RNLYSGDYYRIQG[R/Q]RA 6
distal
737R RNLY[S/R]SGDYYRIQGRA 3
distal
742W RNLYSGDYY[R/W]RIQGRA 2
proximal
742Q RNLYSGDYY[R/Q]RIQGRA 2
proximal

PTM Site: 741Y

Affected site:

Position: 741
Residue: Y
Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation In sequence Distance Impact
740C NLYSGD[Y/C]YYRIQGRAV 1
proximal
746Q NLYSGDYYRIQG[R/Q]RAV 5
distal
737R NLY[S/R]SGDYYRIQGRAV 4
distal
742W NLYSGDYY[R/W]RIQGRAV 1
proximal
742Q NLYSGDYY[R/Q]RIQGRAV 1
proximal

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