ClinVar Miner

List of variants in gene KCNA1 reported as benign by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000217.3(KCNA1):c.1440T>A (p.Thr480=) rs4766309 0.75219
NM_000217.3(KCNA1):c.804G>C (p.Thr268=) rs2227910 0.50318
NM_000217.3(KCNA1):c.*1681T>C rs7974459 0.49866
NM_000217.3(KCNA1):c.*406C>T rs4766311 0.48547
NM_000217.3(KCNA1):c.*3062T>C rs10849174 0.47680
NM_000217.3(KCNA1):c.684T>C (p.Cys228=) rs1048500 0.46819
NM_000217.3(KCNA1):c.*1927A>T rs7974559 0.45881
NM_000217.3(KCNA1):c.*9G>A rs4766310 0.45248
NM_000217.3(KCNA1):c.*4439C>T rs12424292 0.21574
NM_000217.3(KCNA1):c.-110G>A rs35678382 0.12116
NM_000217.3(KCNA1):c.*2174C>T rs73050551 0.04497
NM_000217.3(KCNA1):c.*5141G>A rs41482147 0.04492
NM_000217.3(KCNA1):c.*1524A>G rs79357862 0.04290
NM_000217.3(KCNA1):c.-959C>T rs11831584 0.03555
NM_000217.3(KCNA1):c.-134G>T rs12817318 0.03550
NM_000217.3(KCNA1):c.-731C>G rs74058081 0.03186
NM_000217.3(KCNA1):c.*5145T>C rs11063406 0.02510
NM_000217.3(KCNA1):c.-839C>T rs12303537 0.01982
NM_000217.3(KCNA1):c.*4234A>G rs61907267 0.01618
NM_000217.3(KCNA1):c.*2308C>G rs114342545 0.01314
NM_000217.3(KCNA1):c.*3724C>T rs73050554 0.01288
NM_000217.3(KCNA1):c.*1522C>G rs140297443 0.01151
NM_000217.3(KCNA1):c.*228A>C rs142908193 0.00937
NM_000217.3(KCNA1):c.*2123A>G rs77647135 0.00881
NM_000217.3(KCNA1):c.*1892C>T rs146972463 0.00806
NM_000217.3(KCNA1):c.*2005G>A rs76783799 0.00798
NM_000217.3(KCNA1):c.*2080G>A rs147644839 0.00661
NM_000217.3(KCNA1):c.*1577A>T rs79432803 0.00657
NM_000217.3(KCNA1):c.*786G>A rs148607588 0.00564
NM_000217.3(KCNA1):c.*3840G>A rs148103166 0.00509
NM_000217.3(KCNA1):c.*127A>C rs116918891 0.00476
NM_000217.3(KCNA1):c.*4635G>C rs1045892 0.00438
NM_000217.3(KCNA1):c.*2245C>G rs76258625 0.00350
NM_000217.3(KCNA1):c.-428C>T rs7307690 0.00307
NM_000217.3(KCNA1):c.1296C>G (p.Ser432=) rs76066681 0.00299
NM_000217.3(KCNA1):c.237G>A (p.Glu79=) rs149110871 0.00280
NM_000217.3(KCNA1):c.-1043C>T rs11831571 0.00257
NM_000217.3(KCNA1):c.*189G>A rs187069793 0.00226
NM_000217.3(KCNA1):c.*2727C>T rs113371270 0.00178
NM_000217.3(KCNA1):c.*2121T>C rs188295490 0.00177
NM_000217.3(KCNA1):c.*4591T>G rs150901962 0.00170
NM_000217.3(KCNA1):c.*2596A>T rs188377239 0.00133
NM_000217.3(KCNA1):c.-638C>T rs574980784 0.00118
NM_000217.3(KCNA1):c.-235C>A rs113587682 0.00086
NM_000217.3(KCNA1):c.1327C>G (p.Arg443Gly) rs150849316 0.00078
NM_000217.3(KCNA1):c.1125C>T (p.Tyr375=) rs144351014 0.00038
NM_000217.3(KCNA1):c.*5209C>T rs189939908 0.00025
NM_000217.3(KCNA1):c.*947C>T rs557429239 0.00024
NM_000217.3(KCNA1):c.*2313C>T rs183989674 0.00022
NM_000217.3(KCNA1):c.*4663G>A rs186319441 0.00022
NM_000217.3(KCNA1):c.*592C>A rs144000949 0.00020
NM_000217.3(KCNA1):c.*517T>C rs140164407 0.00002
NM_000217.3(KCNA1):c.*5191G>A rs575078827 0.00002
NM_000217.3(KCNA1):c.*2277_*2278del rs397724146
NM_000217.3(KCNA1):c.*2333G>A rs2109420
NM_000217.3(KCNA1):c.*2734G>A rs115244229

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.