ClinVar Miner

List of variants in gene KCNQ1 reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 68
Download table as spreadsheet
HGVS dbSNP
NM_000218.2(KCNQ1):c.*479G>A rs2519184
NM_000218.2(KCNQ1):c.*875A>G rs8234
NM_000218.2(KCNQ1):c.*932A>G rs10798
NM_000218.2(KCNQ1):c.-5T>C rs532941548
NM_000218.2(KCNQ1):c.1032+11C>T rs201144841
NM_000218.2(KCNQ1):c.1033-12A>G rs200423553
NM_000218.2(KCNQ1):c.1110G>A (p.Ala370=) rs1805118
NM_000218.2(KCNQ1):c.1128+4C>T rs201590918
NM_000218.2(KCNQ1):c.1129-8G>A rs200612600
NM_000218.2(KCNQ1):c.1179G>T (p.Lys393Asn) rs12720457
NM_000218.2(KCNQ1):c.1189C>T (p.Arg397Trp) rs199472776
NM_000218.2(KCNQ1):c.1222C>G (p.Pro408Ala) rs28730756
NM_000218.2(KCNQ1):c.1251+248G>A
NM_000218.2(KCNQ1):c.1252-301T>C
NM_000218.2(KCNQ1):c.1252-60G>A
NM_000218.2(KCNQ1):c.1332G>A (p.Thr444=) rs144985256
NM_000218.2(KCNQ1):c.1343C>G (p.Pro448Arg) rs12720449
NM_000218.2(KCNQ1):c.1515-218A>G
NM_000218.2(KCNQ1):c.1515-31C>G
NM_000218.2(KCNQ1):c.1590+14T>C rs11024034
NM_000218.2(KCNQ1):c.160_168dup (p.Ile54_Pro56dup) rs397515877
NM_000218.2(KCNQ1):c.1638G>A (p.Ser546=) rs1057128
NM_000218.2(KCNQ1):c.1685+282C>T
NM_000218.2(KCNQ1):c.1686-49C>T
NM_000218.2(KCNQ1):c.1732+186A>G
NM_000218.2(KCNQ1):c.1749C>T (p.Arg583=) rs200670744
NM_000218.2(KCNQ1):c.1794+11G>A rs186188610
NM_000218.2(KCNQ1):c.1794+245T>C
NM_000218.2(KCNQ1):c.1795-119T>C
NM_000218.2(KCNQ1):c.1795-298A>G
NM_000218.2(KCNQ1):c.1800G>A (p.Thr600=) rs147091980
NM_000218.2(KCNQ1):c.1860C>T (p.His620=) rs139893266
NM_000218.2(KCNQ1):c.1926C>T (p.Cys642=) rs12720454
NM_000218.2(KCNQ1):c.1927G>A (p.Gly643Ser) rs1800172
NM_000218.2(KCNQ1):c.1942G>A (p.Val648Ile) rs34150427
NM_000218.2(KCNQ1):c.1944C>T (p.Val648=) rs201698592
NM_000218.2(KCNQ1):c.1986C>G (p.Tyr662Ter) rs11601907
NM_000218.2(KCNQ1):c.1986C>T (p.Tyr662=) rs11601907
NM_000218.2(KCNQ1):c.207G>T (p.Ala69=) rs587781009
NM_000218.2(KCNQ1):c.225T>C (p.Val75=) rs367817352
NM_000218.2(KCNQ1):c.386+14C>T rs370023636
NM_000218.2(KCNQ1):c.386+15671G>A
NM_000218.2(KCNQ1):c.386+15841G>A
NM_000218.2(KCNQ1):c.386+16216G>A rs201090517
NM_000218.2(KCNQ1):c.386+16242G>A rs116103203
NM_000218.2(KCNQ1):c.387-18C>T rs377350869
NM_000218.2(KCNQ1):c.435C>T (p.Ile145=) rs1800170
NM_000218.2(KCNQ1):c.447C>T (p.Ala149=) rs146436765
NM_000218.2(KCNQ1):c.459G>A (p.Thr153=) rs148121889
NM_000218.2(KCNQ1):c.477+9C>T rs28730664
NM_000218.2(KCNQ1):c.478-10G>A rs28730752
NM_000218.2(KCNQ1):c.478-212C>T
NM_000218.2(KCNQ1):c.478-299_478-298insCCTCTGGCCAAGGCTGGGGTTCCTGGTGTGGGGCCT
NM_000218.2(KCNQ1):c.478-8C>T rs150711844
NM_000218.2(KCNQ1):c.513C>T (p.Tyr171=) rs139042529
NM_000218.2(KCNQ1):c.552C>T (p.Tyr184=) rs780231722
NM_000218.2(KCNQ1):c.604+220A>C
NM_000218.2(KCNQ1):c.605-11G>A rs200828849
NM_000218.2(KCNQ1):c.605-182T>G
NM_000218.2(KCNQ1):c.605-24C>T
NM_000218.2(KCNQ1):c.683+20T>C rs184516288
NM_000218.2(KCNQ1):c.684-234C>T
NM_000218.2(KCNQ1):c.720C>T (p.His240=) rs28730754
NM_000218.2(KCNQ1):c.781-19TG[2] rs727503103
NM_000218.2(KCNQ1):c.811C>T (p.Leu271=) rs189991547
NM_000218.2(KCNQ1):c.921+7C>T rs370506451
NM_000218.2(KCNQ1):c.922-228A>G
NM_000218.2(KCNQ1):c.972C>T (p.Val324=) rs554518844

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.