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Mutation:
CACNB2 T59A
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: 58S
Affected site:
Position: 58
Residue: S
Type: phosphorylation
Impact:
proximalOther 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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