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Mutation:
NSRP1 S456N
Summary
Clinical Information
Cancer types: (TCGA MC3)
no data
Cancer types: (PCAWG)
Liver-HCC
Disease Annotations: (ClinVar)
no data
Minor Allele Frequency: (ESP6500)
no data
Minor Allele Frequency: (1000 Genomes)
no data
PTM Site: 463K
Affected site:
Position: 463
Residue: K
Type: methylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 458Q | SS[P/Q]PNSRAKDKFLDQE | 5 |
distal
|
| 464N | SSPNSRAK[D/N]DKFLDQE | 1 |
proximal
|
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