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Summary

Isoform:
Position:
332
Ref:
S
Mutation:
N
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)

no data

Minor Allele Frequency: (1000 Genomes)

[0.0199681]

PTM Site: 333K

Affected site:

Position: 333
Residue: K
Type: ubiquitination

Impact:

proximal

Other known mutations affecting this site

Mutation In sequence Distance Impact
338M EQKKISSKINYS[V/M]VLR 5
distal
337T EQKKISSKINY[S/T]SVLR 4
distal
332N EQKKIS[S/N]SKINYSVLR 1
proximal

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