ClinVar Miner

List of variants in gene KCNQ2 reported as likely benign for Seizures

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Total variants: 23
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HGVS dbSNP
NM_172107.3(KCNQ2):c.128C>T (p.Ala43Val) rs749554385
NM_172107.3(KCNQ2):c.2119G>A (p.Ala707Thr)
NM_172107.3(KCNQ2):c.2266G>A (p.Gly756Ser) rs200909197
NM_172107.4(KCNQ2):c.*4G>A rs1801508
NM_172107.4(KCNQ2):c.1419C>T (p.Leu473=) rs370155790
NM_172107.4(KCNQ2):c.1587C>T (p.Thr529=) rs753417293
NM_172107.4(KCNQ2):c.1833G>A (p.Ala611=) rs564630217
NM_172107.4(KCNQ2):c.1842C>T (p.Pro614=) rs552807375
NM_172107.4(KCNQ2):c.2031G>A (p.Arg677=) rs35647984
NM_172107.4(KCNQ2):c.2065A>C (p.Ile689Leu) rs201701585
NM_172107.4(KCNQ2):c.2076C>T (p.Ser692=) rs1568861472
NM_172107.4(KCNQ2):c.2121G>A (p.Ala707=) rs1269199299
NM_172107.4(KCNQ2):c.2529C>T (p.Ser843=) rs140674819
NM_172107.4(KCNQ2):c.2544G>A (p.Pro848=) rs147274045
NM_172107.4(KCNQ2):c.303C>G (p.Leu101=) rs145415996
NM_172107.4(KCNQ2):c.570C>T (p.Asn190=) rs116087798
NM_172107.4(KCNQ2):c.627C>A (p.Ile209=)
NM_172107.4(KCNQ2):c.681C>T (p.Ala227=) rs1472366685
NM_172107.4(KCNQ2):c.705C>T (p.Ala235=) rs1291672036
NM_172107.4(KCNQ2):c.754T>C (p.Leu252=) rs370174915
NM_172107.4(KCNQ2):c.774C>T (p.Asn258=) rs770187706
NM_172107.4(KCNQ2):c.792C>T (p.Tyr264=) rs143399744
NM_172107.4(KCNQ2):c.81G>A (p.Leu27=) rs373897282

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