List of variants in gene KCNA5 reported as benign for atrial fibrillation (disease)

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: 21

Download table as spreadsheet

HGVS	dbSNP
NM_002234.4(KCNA5):c.*508A>T	rs1056468
NM_002234.4(KCNA5):c.*736A>T	rs66942317
NM_002234.4(KCNA5):c.-167C>T	rs3741930
NM_002234.4(KCNA5):c.1020C>T (p.Leu340=)	rs72546671
NM_002234.4(KCNA5):c.1149T>C (p.Gly383=)	rs2359641
NM_002234.4(KCNA5):c.1149_1150inv (p.Gly384Arg)
NM_002234.4(KCNA5):c.1150G>A (p.Gly384Arg)	rs76708779
NM_002234.4(KCNA5):c.1170G>A (p.Gly390=)	rs200060072
NM_002234.4(KCNA5):c.1353C>G (p.Ala451=)	rs767826909
NM_002234.4(KCNA5):c.1353C>T (p.Ala451=)	rs767826909
NM_002234.4(KCNA5):c.1497G>A (p.Leu499=)	rs17221805
NM_002234.4(KCNA5):c.1733G>A (p.Arg578Lys)	rs12720445
NM_002234.4(KCNA5):c.180G>A (p.Ala60=)	rs376660949
NM_002234.4(KCNA5):c.207G>T (p.Pro69=)	rs757133156
NM_002234.4(KCNA5):c.229C>T (p.Pro77Ser)	rs202083721
NM_002234.4(KCNA5):c.381C>T (p.Ser127=)	rs45504599
NM_002234.4(KCNA5):c.570C>T (p.Asn190=)	rs12720444
NM_002234.4(KCNA5):c.615G>C (p.Leu205=)	rs12720443
NM_002234.4(KCNA5):c.751G>A (p.Ala251Thr)	rs12720442
NM_002234.4(KCNA5):c.929C>T (p.Pro310Leu)	rs17215402
NM_002234.4(KCNA5):c.92G>T (p.Gly31Val)	rs61737395

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.