ClinVar Miner

Submissions for variant NM_016507.4(CDK12):c.3997C>T (p.Arg1333Cys)

gnomAD frequency: 0.00090 dbSNP: rs142347393

Minimum review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
ITMI	RCV000120524	SCV000084677	not provided	not specified	2013-09-19	no assertion provided	reference population

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