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Mutation:
NT5C2 E501D
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
no data
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
[0.0077]
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 502S
Affected site:
Position: 502
Residue: S
Type: phosphorylation
Impact:
proximalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 501D | VDINEM[E/D]ESPLATRNR | 1 |
proximal
|
| 503A | VDINEMES[P/A]PLATRNR | 1 |
network-rewiring
|
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