ClinVar Miner

List of variants studied for Atrial fibrillation, familial, 7 by Fulgent Genetics, Fulgent Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 44
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002234.4(KCNA5):c.79G>A (p.Gly27Ser) rs201238766 0.00105
NM_002234.4(KCNA5):c.260G>A (p.Arg87Gln) rs71537801 0.00029
NM_002234.4(KCNA5):c.98A>T (p.Glu33Val) rs71584818 0.00020
NM_002234.4(KCNA5):c.701G>T (p.Arg234Leu) rs371521698 0.00012
NM_002234.4(KCNA5):c.797C>T (p.Thr266Ile) rs369750762 0.00012
NM_002234.4(KCNA5):c.28A>G (p.Asn10Asp) rs894679405 0.00011
NM_002234.4(KCNA5):c.1327A>G (p.Ile443Val) rs370591031 0.00010
NM_002234.4(KCNA5):c.196C>T (p.Pro66Ser) rs368699451 0.00010
NM_002234.4(KCNA5):c.926G>A (p.Gly309Asp) rs369120527 0.00010
NM_002234.4(KCNA5):c.1730G>A (p.Arg577Gln) rs139805781 0.00009
NM_002234.4(KCNA5):c.41T>G (p.Met14Arg) rs995191067 0.00008
NM_002234.4(KCNA5):c.1573C>T (p.Arg525Trp) rs376656991 0.00007
NM_002234.4(KCNA5):c.913G>A (p.Ala305Thr) rs199794307 0.00007
NM_002234.4(KCNA5):c.193C>T (p.Arg65Trp) rs539270866 0.00006
NM_002234.4(KCNA5):c.917C>A (p.Pro306Gln) rs527534559 0.00006
NM_002234.4(KCNA5):c.1580C>T (p.Thr527Met) rs121908591 0.00005
NM_002234.4(KCNA5):c.1660C>T (p.Arg554Trp) rs150208806 0.00004
NM_002234.4(KCNA5):c.1789C>T (p.Arg597Trp) rs759691488 0.00004
NM_002234.4(KCNA5):c.347C>T (p.Ser116Phe) rs962908688 0.00004
NM_002234.4(KCNA5):c.551G>A (p.Arg184His) rs375080039 0.00004
NM_002234.4(KCNA5):c.1A>G (p.Met1Val) rs889711431 0.00003
NM_002234.4(KCNA5):c.1282C>T (p.Gln428Ter) rs377498745 0.00002
NM_002234.4(KCNA5):c.398C>A (p.Thr133Lys) rs781073587 0.00002
NM_002234.4(KCNA5):c.*244C>T rs992233743 0.00001
NM_002234.4(KCNA5):c.1138C>G (p.Gln380Glu) rs1448543777 0.00001
NM_002234.4(KCNA5):c.1190C>T (p.Ala397Val) rs748288439 0.00001
NM_002234.4(KCNA5):c.1286C>T (p.Ala429Val) rs745704941 0.00001
NM_002234.4(KCNA5):c.160C>T (p.Arg54Cys) rs1357336410 0.00001
NM_002234.4(KCNA5):c.1727C>T (p.Ala576Val) rs121908592 0.00001
NM_002234.4(KCNA5):c.214G>C (p.Asp72His) rs758310507 0.00001
NM_002234.4(KCNA5):c.460C>A (p.Arg154Ser) rs756977657 0.00001
NM_002234.4(KCNA5):c.754A>G (p.Ile252Val) rs1555100234 0.00001
NM_002234.4(KCNA5):c.886C>T (p.Pro296Ser) rs1172777549 0.00001
NM_002234.4(KCNA5):c.*782G>A rs189015926
NM_002234.4(KCNA5):c.1043G>A (p.Ser348Asn) rs755829081
NM_002234.4(KCNA5):c.1084G>A (p.Val362Met) rs776815613
NM_002234.4(KCNA5):c.1681G>C (p.Gly561Arg) rs1440776773
NM_002234.4(KCNA5):c.1704dup (p.Thr569fs) rs1565466174
NM_002234.4(KCNA5):c.1826G>C (p.Arg609Pro) rs991950771
NM_002234.4(KCNA5):c.403_405del (p.Leu135del) rs1451178605
NM_002234.4(KCNA5):c.459_460delinsAA (p.Arg154Ser) rs1862749418
NM_002234.4(KCNA5):c.847C>T (p.Arg283Cys) rs886049575
NM_002234.4(KCNA5):c.859_860delinsTT (p.Ala287Leu) rs1565465582
NM_002234.4(KCNA5):c.964G>C (p.Asp322His) rs139614200

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.