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Mutation:
COPB1 I116L
Summary
Isoform:
Position:
116
Ref:
I
Mutation:
L
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)
[0.0399361]
PTM Site: 117R
Affected site:
Position: 117
Residue: R
Type: methylation
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 116L | QHPNEF[I/L]IRGSTLRFL | 1 |
proximal
|
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