List of variants in gene PRDM16 reported as likely 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: 27

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_022114.4(PRDM16):c.1684G>A (p.Val562Ile)	rs150395260	0.00159
NM_022114.4(PRDM16):c.201G>A (p.Pro67=)	rs199614349	0.00153
NM_022114.4(PRDM16):c.1134C>G (p.Ser378=)	rs200169663	0.00088
NM_022114.4(PRDM16):c.2296G>A (p.Gly766Ser)	rs199998420	0.00081
NM_022114.4(PRDM16):c.2634C>T (p.Pro878=)	rs201338158	0.00065
NM_022114.4(PRDM16):c.142G>A (p.Val48Met)	rs199968728	0.00051
NM_022114.4(PRDM16):c.3110-4G>A	rs201495178	0.00046
NM_022114.4(PRDM16):c.102G>A (p.Ala34=)	rs374918897	0.00040
NM_022114.4(PRDM16):c.3109+9C>T	rs369808146	0.00021
NM_022114.4(PRDM16):c.252C>T (p.Phe84=)	rs370290776	0.00017
NM_022114.4(PRDM16):c.1578G>A (p.Pro526=)	rs376747653	0.00016
NM_022114.4(PRDM16):c.2154G>A (p.Ser718=)	rs781041726	0.00014
NM_022114.4(PRDM16):c.1363G>A (p.Gly455Ser)	rs536908705	0.00013
NM_022114.4(PRDM16):c.714C>A (p.Leu238=)	rs371540074	0.00010
NM_022114.4(PRDM16):c.2856G>A (p.Thr952=)	rs563342786	0.00009
NM_022114.4(PRDM16):c.1839C>T (p.Thr613=)	rs549179676	0.00007
NM_022114.4(PRDM16):c.3135G>A (p.Thr1045=)	rs761078027	0.00007
NM_022114.4(PRDM16):c.3366C>T (p.Asp1122=)	rs370195954	0.00006
NM_022114.4(PRDM16):c.822C>T (p.Gly274=)	rs372730781	0.00006
NM_022114.4(PRDM16):c.1116G>A (p.Gly372=)	rs757093442	0.00002
NM_022114.4(PRDM16):c.1977G>A (p.Pro659=)	rs759550479	0.00001
NM_022114.4(PRDM16):c.2106G>A (p.Lys702=)	rs776564044	0.00001
NM_022114.4(PRDM16):c.657A>C (p.Thr219=)	rs777464880	0.00001
NM_022114.4(PRDM16):c.666C>T (p.Pro222=)	rs876657565	0.00001
NM_022114.4(PRDM16):c.1983C>T (p.Ser661=)	rs764211215
NM_022114.4(PRDM16):c.2468G>C (p.Arg823Pro)	rs371654192
NM_022114.4(PRDM16):c.3109+12G>C	rs200643126

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.