List of variants in gene RAD21 reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_006265.3(RAD21):c.1864G>A (p.Ala622Thr)	rs775266057	0.00001
NM_006265.3(RAD21):c.1127C>G (p.Pro376Arg)	rs387907212
NM_006265.3(RAD21):c.1217_1224del (p.Lys406fs)	rs1812376090
NM_006265.3(RAD21):c.1548delinsTC (p.Glu518fs)	rs1812331711
NM_006265.3(RAD21):c.1621-384_1704+199del	rs2537284941
NM_006265.3(RAD21):c.1753T>C (p.Cys585Arg)	rs387907213
NM_006265.3(RAD21):c.1774_1776del (p.Gln592del)	rs1563686762
NM_006265.3(RAD21):c.1843G>T (p.Glu615Ter)	rs1425483905
NM_006265.3(RAD21):c.589C>T (p.Gln197Ter)	rs1352385210
NM_006265.3(RAD21):c.593dup (p.Ser198fs)	rs2130469261
NM_006265.3(RAD21):c.704del (p.Ser235fs)	rs1812478613
NM_006265.3(RAD21):c.943_946del (p.Glu315fs)	rs2130463115

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.