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Summary

Isoform:
Position:
147
Ref:
E
Mutation:
G
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: 148K

Affected site:

Position: 148
Residue: K
Type: ubiquitination

Impact:

proximal

Other known mutations affecting this site

Mutation In sequence Distance Impact
145A QRIH[T/A]TGEKPYECNQC 3
distal
153S QRIHTGEKPYEC[N/S]NQC 5
distal
147G QRIHTG[E/G]EKPYECNQC 1
proximal
150H QRIHTGEKP[Y/H]YECNQC 2
proximal

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