List of variants in gene PDYN reported as likely benign for not provided

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: 33

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_024411.5(PDYN):c.575A>T (p.Glu192Val)	rs45469293	0.00704
NM_024411.5(PDYN):c.436A>C (p.Met146Leu)	rs77155664	0.00698
NM_024411.5(PDYN):c.121A>G (p.Asn41Asp)	rs59191035	0.00237
NM_024411.5(PDYN):c.106G>T (p.Gly36Cys)	rs149056587	0.00062
NM_024411.5(PDYN):c.271C>T (p.Pro91Ser)	rs147355936	0.00028
NM_024411.5(PDYN):c.691C>A (p.Arg231=)	rs201204862	0.00022
NM_024411.5(PDYN):c.716G>A (p.Arg239Gln)	rs185551108	0.00014
NM_024411.5(PDYN):c.483C>G (p.Leu161=)	rs773513924	0.00010
NM_024411.5(PDYN):c.294C>A (p.Leu98=)	rs1013556777	0.00005
NM_024411.5(PDYN):c.300G>T (p.Gly100=)	rs182230231	0.00005
NM_024411.5(PDYN):c.74G>A (p.Arg25Gln)	rs369559888	0.00005
NM_024411.5(PDYN):c.162G>A (p.Leu54=)	rs368889501	0.00003
NM_024411.5(PDYN):c.456C>T (p.Asn152=)	rs148113209	0.00002
NM_024411.5(PDYN):c.708G>A (p.Val236=)	rs150953132	0.00002
NM_024411.5(PDYN):c.129+8T>C	rs747450086	0.00001
NM_024411.5(PDYN):c.138C>T (p.Ser46=)	rs746996074	0.00001
NM_024411.5(PDYN):c.378G>A (p.Leu126=)	rs1359072362	0.00001
NM_024411.5(PDYN):c.607C>T (p.Leu203=)	rs1185514961	0.00001
NM_024411.5(PDYN):c.729T>C (p.Asp243=)	rs754301697	0.00001
NM_024411.5(PDYN):c.73C>T (p.Arg25Trp)	rs1028619685	0.00001
NM_024411.5(PDYN):c.120C>T (p.Ile40=)	rs2514350348
NM_024411.5(PDYN):c.162G>T (p.Leu54=)	rs368889501
NM_024411.5(PDYN):c.192C>T (p.Ser64=)	rs1987729572
NM_024411.5(PDYN):c.198G>A (p.Leu66=)	rs764790414
NM_024411.5(PDYN):c.393G>A (p.Arg131=)	rs1987705572
NM_024411.5(PDYN):c.405C>T (p.Asp135=)	rs147181436
NM_024411.5(PDYN):c.444T>C (p.Asp148=)	rs1166439244
NM_024411.5(PDYN):c.489C>T (p.Leu163=)	rs774940143
NM_024411.5(PDYN):c.528G>A (p.Gly176=)	rs2514335634
NM_024411.5(PDYN):c.561A>C (p.Ser187=)	rs1600504981
NM_024411.5(PDYN):c.582C>T (p.Asp194=)	rs769461186
NM_024411.5(PDYN):c.612C>T (p.Tyr204=)
NM_024411.5(PDYN):c.618C>G (p.Arg206=)	rs1279805007

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.