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Summary

Isoform:
Position:
437
Ref:
H
Mutation:
L
PTM impact:
proximal
PTM affected:
2
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

LUAD

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: 431K

Affected site:

Position: 431
Residue: K
Type: ubiquitination

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
436M QLIRESLKVALQ[K/M]KHS 5
distal
437L QLIRESLKVALQK[H/L]HS 6
distal

PTM Site: 436K

Affected site:

Position: 436
Residue: K
Type: ubiquitination

Impact:

proximal

Other known mutations affecting this site

Mutation In sequence Distance Impact
436M SLKVALQ[K/M]KHSEEVKK 0
direct
437L SLKVALQK[H/L]HSEEVKK 1
proximal

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