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Summary

Isoform:
Position:
398
Ref:
S
Mutation:
A
PTM impact:
proximal
PTM affected:
2
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

no data

Minor Allele Frequency: (ESP6500)

[0.05]

Minor Allele Frequency: (1000 Genomes)

[0.059904200000000005]

PTM Site: 393T

Affected site:

Position: 393
Residue: T
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
389R KSL[T/R]TEISTDFDRSSP 4
distal
391T KSLTE[I/T]ISTDFDRSSP 2
proximal
397C KSLTEISTDFD[R/C]RSSP 4
distal
397H KSLTEISTDFD[R/H]RSSP 4
distal
398A KSLTEISTDFDR[S/A]SSP 5
distal
393A KSLTEIS[T/A]TDFDRSSP 0
direct
390V KSLT[E/V]EISTDFDRSSP 3
distal
388F KS[L/F]LTEISTDFDRSSP 5
distal
393I KSLTEIS[T/I]TDFDRSSP 0
direct

PTM Site: 399S

Affected site:

Position: 399
Residue: S
Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation In sequence Distance Impact
397C STDFD[R/C]RSSPPLQPPP 2
network-rewiring
397H STDFD[R/H]RSSPPLQPPP 2
network-rewiring
398A STDFDR[S/A]SSPPLQPPP 1
proximal
393A S[T/A]TDFDRSSPPLQPPP 6
distal
393I S[T/I]TDFDRSSPPLQPPP 6
distal

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