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Mutation:
MIF4GD D222N
Summary
Isoform:
Position:
222
Ref:
D
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: 221S
Affected site:
Position: 221
Residue: S
Type: phosphorylation
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 219D | KYYYS[E/D]EVSD------ | 2 |
proximal
|
| 222N | KYYYSEVS[D/N]D------ | 1 |
proximal
|
| 220A | KYYYSE[V/A]VSD------ | 1 |
proximal
|
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