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Mutation:
CEP85 K436M
Summary
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: 431K
Affected site:
Position: 431
Residue: K
Type: ubiquitination
Impact:
distalOther 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:
directOther 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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