List of variants in gene DNAJC5 reported as likely benign by Ambry Genetics

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_025219.3(DNAJC5):c.132C>T (p.Pro44=)	rs140948457	0.00314
NM_025219.3(DNAJC5):c.456C>T (p.Pro152=)	rs140326040	0.00130
NM_025219.3(DNAJC5):c.45A>G (p.Ser15=)	rs144141585	0.00066
NM_025219.3(DNAJC5):c.282C>T (p.Asn94=)	rs113207069	0.00051
NM_025219.3(DNAJC5):c.228C>T (p.Tyr76=)	rs201495666	0.00031
NM_025219.3(DNAJC5):c.531C>T (p.Ser177=)	rs376694698	0.00012
NM_025219.3(DNAJC5):c.75C>T (p.Asn25=)	rs189308547	0.00010
NM_025219.3(DNAJC5):c.513C>T (p.Ile171=)	rs745794091	0.00005
NM_025219.3(DNAJC5):c.447C>T (p.Tyr149=)	rs780478210	0.00002
NM_025219.3(DNAJC5):c.561C>T (p.Asp187=)	rs776807695	0.00001
NM_025219.3(DNAJC5):c.252C>G (p.Leu84=)
NM_025219.3(DNAJC5):c.438G>A (p.Thr146=)	rs746222594
NM_025219.3(DNAJC5):c.504C>T (p.Asp168=)	rs886056935

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