ClinVar Miner

List of variants in gene DNAJC12 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_021800.3(DNAJC12):c.347C>A (p.Ser116Tyr)
NM_021800.3(DNAJC12):c.503G>T (p.Gly168Val)
NM_021800.3(DNAJC12):c.538C>T (p.Arg180Cys)

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