ClinVar Miner

Submissions for variant NM_002739.5(PRKCG):c.303C>G (p.His101Gln)

dbSNP: rs121918518
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000014156 SCV000034404 pathogenic Spinocerebellar ataxia type 14 2005-01-01 no assertion criteria provided literature only
GeneReviews RCV000014156 SCV000058618 not provided Spinocerebellar ataxia type 14 no assertion provided literature only

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