ClinVar Miner

List of variants in gene KCNQ1 reported as uncertain significance for not specified

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Total variants: 42
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HGVS dbSNP
NM_000218.2(KCNQ1):c.136G>A (p.Ala46Thr) rs199473671
NM_000218.2(KCNQ1):c.1498A>G
NM_000218.2(KCNQ1):c.181C>A (p.Pro61Thr) rs1273257287
NM_000218.2(KCNQ1):c.1888C>T
NM_000218.2(KCNQ1):c.1923delC
NM_000218.2(KCNQ1):c.19C>T (p.Pro7Ser) rs199473443
NM_000218.2(KCNQ1):c.217C>A (p.Pro73Thr) rs199472676
NM_000218.2(KCNQ1):c.285C>A
NM_000218.2(KCNQ1):c.328G>A (p.Val110Ile) rs199472677
NM_000218.2(KCNQ1):c.347G>A (p.Arg116His) rs727504506
NM_181798.1(KCNQ1):c.103G>A (p.Val35Met) rs199472692
NM_181798.1(KCNQ1):c.112G>A (p.Val38Met) rs1085307580
NM_181798.1(KCNQ1):c.1156A>T (p.Thr386Ser) rs778975231
NM_181798.1(KCNQ1):c.1174C>T (p.Arg392Cys) rs199472787
NM_181798.1(KCNQ1):c.1240G>A (p.Val414Ile) rs199472796
NM_181798.1(KCNQ1):c.1351G>A (p.Glu451Lys) rs1057517750
NM_181798.1(KCNQ1):c.1387G>A (p.Ala463Thr) rs199472813
NM_181798.1(KCNQ1):c.1418C>T (p.Thr473Met) rs34516117
NM_181798.1(KCNQ1):c.1450G>A (p.Asp484Asn) rs147445322
NM_181798.1(KCNQ1):c.1480G>A (p.Gly494Ser) rs199472820
NM_181798.1(KCNQ1):c.1522G>A (p.Gly508Arg) rs199473484
NM_181798.1(KCNQ1):c.1545C>G (p.Cys515Trp) rs12720454
NM_181798.1(KCNQ1):c.1605C>G (p.Tyr535Ter) rs11601907
NM_181798.1(KCNQ1):c.193C>T (p.Arg65Cys)
NM_181798.1(KCNQ1):c.267C>A (p.Gly89=) rs146350010
NM_181798.1(KCNQ1):c.39C>T (p.Ser13=) rs377520734
NM_181798.1(KCNQ1):c.439A>G (p.Ile147Val) rs199472728
NM_181798.1(KCNQ1):c.479C>A (p.Ala160Glu) rs199472735
NM_181798.1(KCNQ1):c.487G>A (p.Glu163Lys) rs199473464
NM_181798.1(KCNQ1):c.517G>A (p.Ala173Thr) rs120074187
NM_181798.1(KCNQ1):c.541-3C>A rs794728515
NM_181798.1(KCNQ1):c.577C>T (p.Pro193Ser) rs199472753
NM_181798.1(KCNQ1):c.650C>A (p.Ala217Glu) rs199472763
NM_181798.1(KCNQ1):c.724C>G (p.Pro242Ala) rs794728525
NM_181798.1(KCNQ1):c.748-8G>A rs200612600
NM_181798.1(KCNQ1):c.77C>T (p.Thr26Met) rs143709408
NM_181798.1(KCNQ1):c.808C>T (p.Arg270Trp) rs199472776
NM_181798.1(KCNQ1):c.815C>G (p.Ala272Gly) rs876657836
NM_181798.1(KCNQ1):c.820C>T (p.Arg274Trp) rs766616232
NM_181798.1(KCNQ1):c.821G>A (p.Arg274Gln) rs542628042
NM_181798.1(KCNQ1):c.914C>T (p.Thr305Ile) rs751644427
NM_181798.1(KCNQ1):c.940C>T (p.Pro314Ser) rs199473475

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