ClinVar Miner

List of variants in gene KCNQ1 reported by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 79
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HGVS dbSNP
NM_000218.2(KCNQ1):c.-38C>T rs886048160
NM_000218.2(KCNQ1):c.-69G>A rs886048159
NM_000218.2(KCNQ1):c.207G>T (p.Ala69=) rs587781009
NM_000218.2(KCNQ1):c.29C>A (p.Ala10Asp) rs886048161
NM_000218.2(KCNQ1):c.66C>T (p.Gly22=) rs886048162
NM_181798.1(KCNQ1):c.*1025G>C rs181226788
NM_181798.1(KCNQ1):c.*1055C>T rs375155898
NM_181798.1(KCNQ1):c.*1088G>C rs886048177
NM_181798.1(KCNQ1):c.*160C>A rs886048167
NM_181798.1(KCNQ1):c.*171G>A rs886048168
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.*26C>A rs886048166
NM_181798.1(KCNQ1):c.*292C>A rs886048169
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.*391G>A rs774059974
NM_181798.1(KCNQ1):c.*392A>C rs868129989
NM_181798.1(KCNQ1):c.*398C>T rs886048170
NM_181798.1(KCNQ1):c.*411C>T rs45460605
NM_181798.1(KCNQ1):c.*464G>A rs141960532
NM_181798.1(KCNQ1):c.*479G>A rs2519184
NM_181798.1(KCNQ1):c.*47A>C rs754931159
NM_181798.1(KCNQ1):c.*482G>A rs45510192
NM_181798.1(KCNQ1):c.*539G>C rs886048171
NM_181798.1(KCNQ1):c.*554T>G rs886048172
NM_181798.1(KCNQ1):c.*581T>C rs765566577
NM_181798.1(KCNQ1):c.*633G>A rs886048173
NM_181798.1(KCNQ1):c.*652G>A rs886048174
NM_181798.1(KCNQ1):c.*712G>A rs745447199
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.*875A>G rs8234
NM_181798.1(KCNQ1):c.*877C>G rs763163556
NM_181798.1(KCNQ1):c.*887_*889del rs886048175
NM_181798.1(KCNQ1):c.*889_*891AAT[1] rs546360517
NM_181798.1(KCNQ1):c.*897G>T rs561861522
NM_181798.1(KCNQ1):c.*904T>C rs186055804
NM_181798.1(KCNQ1):c.*932A>G rs10798
NM_181798.1(KCNQ1):c.*975C>T rs74048340
NM_181798.1(KCNQ1):c.-16616T>C rs532941548
NM_181798.1(KCNQ1):c.1171C>T (p.Arg391Ter) rs17215500
NM_181798.1(KCNQ1):c.1209+14T>C rs11024034
NM_181798.1(KCNQ1):c.1257G>A (p.Ser419=) rs1057128
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.1413+12C>T rs727505084
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.1592C>A (p.Thr531Asn) rs377661455
NM_181798.1(KCNQ1):c.1598C>A (p.Pro533His) rs886048165
NM_181798.1(KCNQ1):c.1605C>G (p.Tyr535Ter) rs11601907
NM_181798.1(KCNQ1):c.1605C>T (p.Tyr535=) rs11601907
NM_181798.1(KCNQ1):c.175G>A (p.Gly59Ser) rs199473398
NM_181798.1(KCNQ1):c.269C>T (p.Ser90Phe) rs886048163
NM_181798.1(KCNQ1):c.339C>T (p.His113=) rs28730754
NM_181798.1(KCNQ1):c.400-6G>T rs886048164
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.6-7C>T rs201682200
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.808C>T (p.Arg270Trp) rs199472776
NM_181798.1(KCNQ1):c.841C>G (p.Pro281Ala) rs28730756
NM_181798.1(KCNQ1):c.870+13C>T rs201364493
NM_181798.1(KCNQ1):c.96+9C>T rs28730664
NM_181798.1(KCNQ1):c.962C>G (p.Pro321Arg) rs12720449
NM_181798.1(KCNQ1):c.97-10G>A rs28730752
NM_181798.1(KCNQ1):c.97-8C>T rs150711844
NM_181798.1(KCNQ1):c.974G>A (p.Arg325Gln) rs145229963

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