ClinVar Miner

List of variants in gene KCNQ1 reported as likely benign for Long QT syndrome

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Gene type:
ClinVar version:
Total variants: 84
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HGVS dbSNP
NM_000218.2(KCNQ1):c.*219G>A rs45477500
NM_000218.2(KCNQ1):c.*241G>A rs142023323
NM_000218.2(KCNQ1):c.*264T>C rs45579540
NM_000218.2(KCNQ1):c.*266G>A rs113029000
NM_000218.2(KCNQ1):c.*305A>C rs45570140
NM_000218.2(KCNQ1):c.*350G>A rs114877430
NM_000218.2(KCNQ1):c.*377delG rs762386874
NM_000218.2(KCNQ1):c.*411C>T rs45460605
NM_000218.2(KCNQ1):c.*464G>A rs141960532
NM_000218.2(KCNQ1):c.*482G>A rs45510192
NM_000218.2(KCNQ1):c.*717T>G rs189162344
NM_000218.2(KCNQ1):c.*731G>A rs146324627
NM_000218.2(KCNQ1):c.*742G>A rs114844136
NM_000218.2(KCNQ1):c.*806C>T rs539398869
NM_000218.2(KCNQ1):c.*837G>A rs139633955
NM_000218.2(KCNQ1):c.*892_*894delAAT rs546360517
NM_000218.2(KCNQ1):c.*904T>C rs186055804
NM_000218.2(KCNQ1):c.*975C>T rs74048340
NM_000218.2(KCNQ1):c.-5T>C rs532941548
NM_000218.2(KCNQ1):c.1033-4C>T rs543599445
NM_000218.2(KCNQ1):c.1033-5C>G rs764094211
NM_000218.2(KCNQ1):c.105C>A (p.Pro35=) rs968695655
NM_000218.2(KCNQ1):c.1107G>A (p.Pro369=) rs746037904
NM_000218.2(KCNQ1):c.1110G>A (p.Ala370=) rs1805118
NM_000218.2(KCNQ1):c.1152C>T (p.Ala384=) rs144615901
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.1236C>T (p.Pro412=) rs1060503984
NM_000218.2(KCNQ1):c.1343C>G (p.Pro448Arg) rs12720449
NM_000218.2(KCNQ1):c.1383T>C (p.Tyr461=) rs794728527
NM_000218.2(KCNQ1):c.1386C>T (p.Asp462=) rs749631604
NM_000218.2(KCNQ1):c.144C>G (p.Gly48=) rs1060503985
NM_000218.2(KCNQ1):c.1590+14T>C rs11024034
NM_000218.2(KCNQ1):c.1591-5C>T rs1311166904
NM_000218.2(KCNQ1):c.1596G>A (p.Ala532=) rs558452873
NM_000218.2(KCNQ1):c.1608C>T (p.Tyr536=) rs138551008
NM_000218.2(KCNQ1):c.1665C>T (p.Arg555=) rs878853755
NM_000218.2(KCNQ1):c.1707G>A (p.Lys569=) rs1288914203
NM_000218.2(KCNQ1):c.1716G>A (p.Leu572=) rs886039093
NM_000218.2(KCNQ1):c.1749C>T (p.Arg583=) rs200670744
NM_000218.2(KCNQ1):c.1761G>A (p.Thr587=) rs148794853
NM_000218.2(KCNQ1):c.1794+10C>G rs558507741
NM_000218.2(KCNQ1):c.1794+10C>T rs558507741
NM_000218.2(KCNQ1):c.1794+11G>A rs186188610
NM_000218.2(KCNQ1):c.1795-4G>A rs769865006
NM_000218.2(KCNQ1):c.1799C>T (p.Thr600Met) rs34516117
NM_000218.2(KCNQ1):c.1831G>A (p.Asp611Asn) rs147445322
NM_000218.2(KCNQ1):c.1875C>T (p.Pro625=) rs112113213
NM_000218.2(KCNQ1):c.1927G>A (p.Gly643Ser) rs1800172
NM_000218.2(KCNQ1):c.1941C>T (p.Ser647=) rs1386852977
NM_000218.2(KCNQ1):c.1942G>A (p.Val648Ile) rs34150427
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.255G>A (p.Val85=) rs766078716
NM_000218.2(KCNQ1):c.387-7C>T rs201682200
NM_000218.2(KCNQ1):c.396C>T (p.Ile132=) rs1400426641
NM_000218.2(KCNQ1):c.435C>T (p.Ile145=) rs1800170
NM_000218.2(KCNQ1):c.459G>A (p.Thr153=) rs148121889
NM_000218.2(KCNQ1):c.477+9C>T rs28730664
NM_000218.2(KCNQ1):c.478-8C>T rs150711844
NM_000218.2(KCNQ1):c.513C>T (p.Tyr171=) rs139042529
NM_000218.2(KCNQ1):c.525C>T (p.Leu175=) rs751902200
NM_000218.2(KCNQ1):c.535G>A (p.Gly179Ser) rs199473394
NM_000218.2(KCNQ1):c.567G>T (p.Gly189=) rs200669271
NM_000218.2(KCNQ1):c.609C>T (p.Leu203=) rs1060503983
NM_000218.2(KCNQ1):c.612C>T (p.Ile204=) rs199473455
NM_000218.2(KCNQ1):c.619G>A (p.Val207Met) rs75813654
NM_000218.2(KCNQ1):c.642C>T (p.Cys214=) rs775479779
NM_000218.2(KCNQ1):c.648C>A (p.Gly216=) rs146350010
NM_000218.2(KCNQ1):c.684-5C>T rs1212611138
NM_000218.2(KCNQ1):c.720C>T (p.His240=) rs28730754
NM_000218.2(KCNQ1):c.729C>T (p.Arg243=) rs755104170
NM_000218.2(KCNQ1):c.811C>T (p.Leu271=) rs189991547
NM_000218.2(KCNQ1):c.820A>G (p.Ile274Val) rs199472728
NM_000218.2(KCNQ1):c.840G>T (p.Val280=) rs1554893236
NM_000218.2(KCNQ1):c.858C>T (p.Asp286=) rs760047145
NM_000218.2(KCNQ1):c.870G>A (p.Glu290=) rs1438599984
NM_000218.2(KCNQ1):c.900A>C (p.Ala300=) rs727504769
NM_000218.2(KCNQ1):c.921+7C>T rs370506451
NM_000218.2(KCNQ1):c.972C>T (p.Val324=) rs554518844
NM_000218.2(KCNQ1):c.984C>T (p.Ile328=) rs140019543
NM_000218.2(KCNQ1):c.996C>T (p.Phe332=) rs1554894464
NM_000218.2(KCNQ1):c.999T>G (p.Ser333=) rs769230282

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