List of variants in gene PRDM16 reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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_022114.4(PRDM16):c.1597T>C (p.Ser533Pro)	rs870124	0.89071
NM_022114.4(PRDM16):c.3284+15G>T	rs870171	0.31838
NM_022114.4(PRDM16):c.444C>T (p.Ser148=)	rs2282198	0.22946
NM_022114.4(PRDM16):c.1898C>T (p.Pro633Leu)	rs2493292	0.14386
NM_022114.4(PRDM16):c.2502C>T (p.Gly834=)	rs115226069	0.04338
NM_022114.4(PRDM16):c.1113C>T (p.Cys371=)	rs61745281	0.02560
NM_022114.4(PRDM16):c.627C>T (p.His209=)	rs12058363	0.02126
NM_022114.4(PRDM16):c.2793C>T (p.Asn931=)	rs59135929	0.01493
NM_022114.4(PRDM16):c.783C>T (p.Tyr261=)	rs61756439	0.00952
NM_022114.4(PRDM16):c.1071C>T (p.Arg357=)	rs2483221	0.00935
NM_022114.4(PRDM16):c.3109+10G>A	rs7549401	0.00898
NM_022114.4(PRDM16):c.2091A>T (p.Ala697=)	rs35184988	0.00685
NM_022114.4(PRDM16):c.38-15C>T	rs9662053	0.00658
NM_022114.4(PRDM16):c.2673G>A (p.Pro891=)	rs3819970	0.00634
NM_022114.4(PRDM16):c.3369C>T (p.Asp1123=)	rs370420046	0.00537
NM_022114.4(PRDM16):c.1518G>A (p.Thr506=)	rs368589754	0.00469
NM_022114.4(PRDM16):c.1212G>A (p.Thr404=)	rs139129844	0.00438
NM_022114.4(PRDM16):c.3130C>T (p.Leu1044Phe)	rs187400273	0.00386
NM_022114.4(PRDM16):c.387+6C>T	rs369010644	0.00373
NM_022114.4(PRDM16):c.100G>A (p.Ala34Thr)	rs187194973	0.00252
NM_022114.4(PRDM16):c.2506G>A (p.Gly836Ser)	rs114204766	0.00168
NM_022114.4(PRDM16):c.1188T>C (p.Cys396=)	rs201309284	0.00167
NM_022114.4(PRDM16):c.2452G>A (p.Gly818Ser)	rs201904226	0.00160
NM_022114.4(PRDM16):c.3687T>C (p.Ala1229=)	rs188634763	0.00137
NM_022114.4(PRDM16):c.1426C>T (p.Pro476Ser)	rs188908415	0.00131
NM_022114.4(PRDM16):c.2290G>A (p.Val764Met)	rs149333409	0.00117
NM_022114.4(PRDM16):c.429C>T (p.Cys143=)	rs150097149	0.00084
NM_022114.4(PRDM16):c.1709C>T (p.Thr570Met)	rs138655327	0.00011
NM_022114.4(PRDM16):c.3301G>A (p.Val1101Met)	rs201654872	0.00009
NM_022114.4(PRDM16):c.2940-15G>A	rs538723120	0.00004
NM_022114.4(PRDM16):c.2448C>T (p.Asn816=)	rs372189819
NM_022114.4(PRDM16):c.3366CGA[3] (p.Asp1125dup)	rs758774731
NM_022114.4(PRDM16):c.884+39_884+69del	rs765185537

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.