ClinVar Miner

List of variants in gene KCNQ1 reported as not provided for not provided

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Total variants: 29
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HGVS dbSNP
NM_000218.2(KCNQ1):c.328G>A (p.Val110Ile) rs199472677
NM_000218.2(KCNQ1):c.356G>A (p.Gly119Asp) rs199472680
NM_000218.2(KCNQ1):c.385G>A (p.Val129Ile) rs199472683
NM_000218.2(KCNQ1):c.40C>T (p.Arg14Cys) rs199473444
NM_181798.1(KCNQ1):c.1175G>A (p.Arg392His) rs199472788
NM_181798.1(KCNQ1):c.1480G>A (p.Gly494Ser) rs199472820
NM_181798.1(KCNQ1):c.1511_1530del (p.Pro504fs) rs397508103
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.160C>T (p.Arg54Cys) rs199473395
NM_181798.1(KCNQ1):c.198T>A (p.Phe66Leu) rs199473454
NM_181798.1(KCNQ1):c.203G>A (p.Arg68Gln) rs138362632
NM_181798.1(KCNQ1):c.232G>A (p.Val78Met) rs151344631
NM_181798.1(KCNQ1):c.238G>A (p.Val80Met) rs75813654
NM_181798.1(KCNQ1):c.379_387del (p.Val127_Phe129del) rs397508124
NM_181798.1(KCNQ1):c.497G>A (p.Arg166His) rs199473465
NM_181798.1(KCNQ1):c.508G>A (p.Gly170Ser) rs34320941
NM_181798.1(KCNQ1):c.517G>A (p.Ala173Thr) rs120074187
NM_181798.1(KCNQ1):c.622T>C (p.Phe208Leu) rs199472757
NM_181798.1(KCNQ1):c.641C>T (p.Ala214Val) rs12720459
NM_181798.1(KCNQ1):c.77C>T (p.Thr26Met) rs143709408
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.902A>G (p.Asp301Gly) rs199472779
NM_181798.1(KCNQ1):c.940C>T (p.Pro314Ser) rs199473475
NM_181798.1(KCNQ1):c.962C>G (p.Pro321Arg) rs12720449
NM_181798.1(KCNQ1):c.971G>A (p.Arg324Gln) rs199472781
NM_181798.1(KCNQ1):c.974G>A (p.Arg325Gln) rs145229963
NM_181798.1(KCNQ1):c.997G>A (p.Gly333Ser) rs199472783

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