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Summary

Isoform:
Position:
565
Ref:
L
Mutation:
F
PTM impact:
distal
PTM affected:
4
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

HNSC

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: 558S

Affected site:

Position: 558
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
552V A[D/V]DTTAKQSLGSHRAL 6
distal
559R ADTTAKQS[L/R]LGSHRAL 1
proximal

PTM Site: 561S

Affected site:

Position: 561
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
559R TAKQS[L/R]LGSHRALTYT 2
network-rewiring
566S TAKQSLGSHRAL[T/S]TYT 5
distal
565F TAKQSLGSHRA[L/F]LTYT 4
distal

PTM Site: 568T

Affected site:

Position: 568
Residue: T
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
569E SHRALTYT[Q/E]QSAPDLS 1
network-rewiring
571V SHRALTYTQS[A/V]APDLS 3
distal
572S SHRALTYTQSA[P/S]PDLS 4
distal
566S SHRAL[T/S]TYTQSAPDLS 2
proximal
565F SHRA[L/F]LTYTQSAPDLS 3
distal
573H SHRALTYTQSAP[D/H]DLS 5
distal

PTM Site: 570S

Affected site:

Position: 570
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
569E RALTYT[Q/E]QSAPDLSPQ 1
proximal
571V RALTYTQS[A/V]APDLSPQ 1
proximal
572S RALTYTQSA[P/S]PDLSPQ 2
proximal
566S RAL[T/S]TYTQSAPDLSPQ 4
distal
565F RA[L/F]LTYTQSAPDLSPQ 5
distal
573H RALTYTQSAP[D/H]DLSPQ 3
distal

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