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Summary

Isoform:
Position:
575
Ref:
T
Mutation:
M
PTM impact:
direct
PTM affected:
3
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

no data

Minor Allele Frequency: (ESP6500)

[0.0082]

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 569S

Affected site:

Position: 569
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
575M RDIIDYESDVEPE[T/M]TK 6
distal
573S RDIIDYESDVE[P/S]PETK 4
distal
566N RDII[D/N]DYESDVEPETK 3
distal
564S RD[I/S]IIDYESDVEPETK 5
distal
563G R[D/G]DIIDYESDVEPETK 6
distal
574K RDIIDYESDVEP[E/K]ETK 5
distal

PTM Site: 575T

Affected site:

Position: 575
Residue: T
Type: phosphorylation

Impact:

direct

Other known mutations affecting this site

Mutation In sequence Distance Impact
575M ESDVEPE[T/M]TKRLKLAA 0
direct
573S ESDVE[P/S]PETKRLKLAA 2
proximal
574K ESDVEP[E/K]ETKRLKLAA 1
proximal

PTM Site: 579K

Affected site:

Position: 579
Residue: K
Type: ubiquitination

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
575M EPE[T/M]TKRLKLAASEDH 4
distal
573S E[P/S]PETKRLKLAASEDH 6
distal
585Y EPETKRLKLAASE[D/Y]DH 6
distal
583L EPETKRLKLAA[S/L]SEDH 4
distal
574K EP[E/K]ETKRLKLAASEDH 5
distal

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