ClinVar Miner

List of variants in gene KCNQ3 reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 63
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HGVS dbSNP
NM_004519.4(KCNQ3):c.*1066A>G rs886062681
NM_004519.4(KCNQ3):c.*1478G>A rs886062680
NM_004519.4(KCNQ3):c.*2013C>T rs886062679
NM_004519.4(KCNQ3):c.*2266_*2269del rs886062678
NM_004519.4(KCNQ3):c.*2385_*2388del rs763323782
NM_004519.4(KCNQ3):c.*2921T>C rs886062676
NM_004519.4(KCNQ3):c.*3216G>C rs886062675
NM_004519.4(KCNQ3):c.*3217C>T rs886062674
NM_004519.4(KCNQ3):c.*3262G>A rs866041778
NM_004519.4(KCNQ3):c.*3591T>C rs778136645
NM_004519.4(KCNQ3):c.*3672C>T rs886062673
NM_004519.4(KCNQ3):c.*3692T>C rs886062672
NM_004519.4(KCNQ3):c.*3805C>T rs886062671
NM_004519.4(KCNQ3):c.*4008G>A rs886062670
NM_004519.4(KCNQ3):c.*4479C>T rs886062669
NM_004519.4(KCNQ3):c.*4481C>A rs886062668
NM_004519.4(KCNQ3):c.*5466T>A rs886062667
NM_004519.4(KCNQ3):c.*5521C>T rs886062666
NM_004519.4(KCNQ3):c.*5580G>A rs886062665
NM_004519.4(KCNQ3):c.*5761C>T rs746747886
NM_004519.4(KCNQ3):c.*6205G>T rs886062664
NM_004519.4(KCNQ3):c.*6351A>G rs781738692
NM_004519.4(KCNQ3):c.*6460C>T rs763946605
NM_004519.4(KCNQ3):c.*6461G>A rs886062663
NM_004519.4(KCNQ3):c.*6607A>G rs751961648
NM_004519.4(KCNQ3):c.*6831G>A rs529301177
NM_004519.4(KCNQ3):c.*7015G>A rs886062662
NM_004519.4(KCNQ3):c.*716_*717insAACA rs886062688
NM_004519.4(KCNQ3):c.*717_*718CA[17] rs35230760
NM_004519.4(KCNQ3):c.*717_*718CA[20] rs35230760
NM_004519.4(KCNQ3):c.*717_*718CA[21] rs35230760
NM_004519.4(KCNQ3):c.*717_*718CA[23] rs35230760
NM_004519.4(KCNQ3):c.*7243C>G rs886062661
NM_004519.4(KCNQ3):c.*732A>G rs886062687
NM_004519.4(KCNQ3):c.*743C>T rs886062686
NM_004519.4(KCNQ3):c.*7512T>G rs886062660
NM_004519.4(KCNQ3):c.*755_*758del rs886062684
NM_004519.4(KCNQ3):c.*755_*760del rs886062683
NM_004519.4(KCNQ3):c.*757_*758CA[1] rs886062682
NM_004519.4(KCNQ3):c.*7980dup rs886062659
NM_004519.4(KCNQ3):c.-130_-129dup rs886062694
NM_004519.4(KCNQ3):c.-134dup rs886062695
NM_004519.4(KCNQ3):c.-135_-134dup rs886062695
NM_004519.4(KCNQ3):c.-136_-134dup rs886062695
NM_004519.4(KCNQ3):c.-138T>G rs868425061
NM_004519.4(KCNQ3):c.-138del rs886062696
NM_004519.4(KCNQ3):c.-139dup rs879019805
NM_004519.4(KCNQ3):c.-140_-139dup rs879019805
NM_004519.4(KCNQ3):c.-140_-139insTG rs886062697
NM_004519.4(KCNQ3):c.-141_-139dup rs879019805
NM_004519.4(KCNQ3):c.-148_-147insTG rs886062698
NM_004519.4(KCNQ3):c.-156C>T rs886062699
NM_004519.4(KCNQ3):c.-54C>G rs772067108
NM_004519.4(KCNQ3):c.132G>C (p.Gly44=) rs762808143
NM_004519.4(KCNQ3):c.145G>A (p.Asp49Asn) rs886062693
NM_004519.4(KCNQ3):c.1507G>A (p.Gly503Arg) rs773584143
NM_004519.4(KCNQ3):c.170T>C (p.Leu57Pro) rs886062692
NM_004519.4(KCNQ3):c.1809A>G (p.Pro603=) rs886062691
NM_004519.4(KCNQ3):c.1980C>A (p.Thr660=) rs886062690
NM_004519.4(KCNQ3):c.1995G>T (p.Ser665=) rs759776061
NM_004519.4(KCNQ3):c.2079G>A (p.Pro693=) rs145204452
NM_004519.4(KCNQ3):c.2165G>A (p.Arg722Gln) rs377725346
NM_004519.4(KCNQ3):c.2274G>A (p.Val758=) rs886062689

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