ClinVar Miner

List of variants in gene AKAP9 studied for Long QT syndrome 11

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 34
Download table as spreadsheet
HGVS dbSNP
NM_005751.4(AKAP9):c.10118C>A (p.Ser3373Tyr) rs140470576
NM_005751.4(AKAP9):c.10426A>C (p.Arg3476=) rs1063243
NM_005751.4(AKAP9):c.10459G>A (p.Glu3487Lys) rs61757664
NM_005751.4(AKAP9):c.10664A>T (p.Asp3555Val) rs139046510
NM_005751.4(AKAP9):c.10767G>A (p.Leu3589=) rs56198613
NM_005751.4(AKAP9):c.10840A>G (p.Met3614Val) rs34327395
NM_005751.4(AKAP9):c.1389G>T (p.Met463Ile) rs6964587
NM_005751.4(AKAP9):c.139C>T (p.His47Tyr) rs35669569
NM_005751.4(AKAP9):c.1489G>T (p.Glu497Ter) rs730880043
NM_005751.4(AKAP9):c.2284A>G (p.Lys762Glu) rs776287498
NM_005751.4(AKAP9):c.3075C>T (p.Thr1025=) rs1989779
NM_005751.4(AKAP9):c.3118A>G (p.Lys1040Glu) rs1265369157
NM_005751.4(AKAP9):c.3504A>G (p.Glu1168=) rs13245393
NM_005751.4(AKAP9):c.3580G>A (p.Ala1194Thr) rs139965373
NM_005751.4(AKAP9):c.4189C>G (p.Gln1397Glu) rs749340561
NM_005751.4(AKAP9):c.4709C>T (p.Ser1570Leu) rs121908566
NM_005751.4(AKAP9):c.5048C>T (p.Thr1683Met) rs146305558
NM_005751.4(AKAP9):c.510G>C (p.Glu170Asp) rs144888041
NM_005751.4(AKAP9):c.5163-20G>A rs9785013
NM_005751.4(AKAP9):c.5246T>C (p.Ile1749Thr) rs150016098
NM_005751.4(AKAP9):c.5565A>G (p.Glu1855=) rs141094356
NM_005751.4(AKAP9):c.5778C>T (p.Gly1926=) rs10236397
NM_005751.4(AKAP9):c.5978-4A>G rs147494754
NM_005751.4(AKAP9):c.610G>A (p.Asp204Asn) rs148920964
NM_005751.4(AKAP9):c.6439G>C (p.Glu2147Gln)
NM_005751.4(AKAP9):c.6556T>C (p.Ser2186Pro) rs76177450
NM_005751.4(AKAP9):c.6945+8C>T rs733957
NM_005751.4(AKAP9):c.80C>T (p.Ser27Leu) rs142401936
NM_005751.4(AKAP9):c.8286A>C (p.Lys2762Asn) rs144875383
NM_005751.4(AKAP9):c.8375A>G (p.Asn2792Ser) rs6960867
NM_005751.4(AKAP9):c.8485G>A (p.Glu2829Lys) rs149946443
NM_005751.4(AKAP9):c.8665C>T (p.Leu2889=) rs10228334
NM_005751.4(AKAP9):c.8935C>T (p.Pro2979Ser) rs1063242
NM_005751.4(AKAP9):c.9145C>T (p.Leu3049=) rs28927678

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.