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Mutation:
CACNB2 R51G
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: 58S
Affected site:
Position: 58
Residue: S
Type: phosphorylation
Impact:
distalOther known mutations affecting this site
| Mutation | In sequence | Distance | Impact |
|---|---|---|---|
| 59A | RFKGSDGS[T/A]TSSDTTS | 1 |
proximal
|
| 52C | R[F/C]FKGSDGSTSSDTTS | 6 |
distal
|
| 56N | RFKGS[D/N]DGSTSSDTTS | 2 |
proximal
|
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