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Summary

Isoform:
Position:
600
Ref:
I
Mutation:
T
PTM impact:
proximal
PTM affected:
1
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

no data

Minor Allele Frequency: (ESP6500)

[0.0245]

Minor Allele Frequency: (1000 Genomes)

[0.059904200000000005]

PTM Site: 598K

Affected site:

Position: 598
Residue: K
Type: ubiquitination

Impact:

proximal

Other known mutations affecting this site

Mutation In sequence Distance Impact
601Q EETPSQSKQI[R/Q]RTPLV 3
distal
600T EETPSQSKQ[I/T]IRTPLV 2
proximal
593R EE[T/R]TPSQSKQIRTPLV 5
distal

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