ClinVar Miner

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

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Total variants: 36
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HGVS dbSNP
NM_000218.2(KCNQ1):c.207G>T (p.Ala69=) rs587781009
NM_181798.1(KCNQ1):c.*219G>A rs45477500
NM_181798.1(KCNQ1):c.*241G>A rs142023323
NM_181798.1(KCNQ1):c.*264T>C rs45579540
NM_181798.1(KCNQ1):c.*266G>A rs113029000
NM_181798.1(KCNQ1):c.*305A>C rs45570140
NM_181798.1(KCNQ1):c.*350G>A rs114877430
NM_181798.1(KCNQ1):c.*377del rs762386874
NM_181798.1(KCNQ1):c.*411C>T rs45460605
NM_181798.1(KCNQ1):c.*464G>A rs141960532
NM_181798.1(KCNQ1):c.*482G>A rs45510192
NM_181798.1(KCNQ1):c.*717T>G rs189162344
NM_181798.1(KCNQ1):c.*731G>A rs146324627
NM_181798.1(KCNQ1):c.*742G>A rs114844136
NM_181798.1(KCNQ1):c.*806C>T rs539398869
NM_181798.1(KCNQ1):c.*837G>A rs139633955
NM_181798.1(KCNQ1):c.*889_*891AAT[1] rs546360517
NM_181798.1(KCNQ1):c.*904T>C rs186055804
NM_181798.1(KCNQ1):c.*975C>T rs74048340
NM_181798.1(KCNQ1):c.-16616T>C rs532941548
NM_181798.1(KCNQ1):c.1209+14T>C rs11024034
NM_181798.1(KCNQ1):c.132C>T (p.Tyr44=) rs139042529
NM_181798.1(KCNQ1):c.1368C>T (p.Arg456=) rs200670744
NM_181798.1(KCNQ1):c.1413+11G>A rs186188610
NM_181798.1(KCNQ1):c.1494C>T (p.Pro498=) rs112113213
NM_181798.1(KCNQ1):c.1546G>A (p.Gly516Ser) rs1800172
NM_181798.1(KCNQ1):c.1561G>A (p.Val521Ile) rs34150427
NM_181798.1(KCNQ1):c.339C>T (p.His113=) rs28730754
NM_181798.1(KCNQ1):c.54C>T (p.Ile18=) rs1800170
NM_181798.1(KCNQ1):c.591C>T (p.Val197=) rs554518844
NM_181798.1(KCNQ1):c.729G>A (p.Ala243=) rs1805118
NM_181798.1(KCNQ1):c.78G>A (p.Thr26=) rs148121889
NM_181798.1(KCNQ1):c.798G>T (p.Lys266Asn) rs12720457
NM_181798.1(KCNQ1):c.841C>G (p.Pro281Ala) rs28730756
NM_181798.1(KCNQ1):c.96+9C>T rs28730664
NM_181798.1(KCNQ1):c.97-8C>T rs150711844

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