ClinVar Miner

List of variants in gene KCNQ1 reported as uncertain significance by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Total variants: 27
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HGVS dbSNP
NM_000218.2(KCNQ1):c.1129-8G>A rs200612600
NM_000218.2(KCNQ1):c.1189C>T (p.Arg397Trp) rs199472776
NM_000218.2(KCNQ1):c.1196C>G (p.Ala399Gly) rs876657836
NM_000218.2(KCNQ1):c.1201C>T (p.Arg401Trp) rs766616232
NM_000218.2(KCNQ1):c.1202G>A (p.Arg401Gln) rs542628042
NM_000218.2(KCNQ1):c.1295C>T (p.Thr432Ile) rs751644427
NM_000218.2(KCNQ1):c.136G>A (p.Ala46Thr) rs199473671
NM_000218.2(KCNQ1):c.1498A>G
NM_000218.2(KCNQ1):c.1555C>T (p.Arg519Cys) rs199472787
NM_000218.2(KCNQ1):c.1621G>A (p.Val541Ile) rs199472796
NM_000218.2(KCNQ1):c.181C>A (p.Pro61Thr) rs1273257287
NM_000218.2(KCNQ1):c.1831G>A (p.Asp611Asn) rs147445322
NM_000218.2(KCNQ1):c.1888C>T
NM_000218.2(KCNQ1):c.1903G>A (p.Gly635Arg) rs199473484
NM_000218.2(KCNQ1):c.1923delC
NM_000218.2(KCNQ1):c.1926C>G (p.Cys642Trp) rs12720454
NM_000218.2(KCNQ1):c.1986C>G (p.Tyr662Ter) rs11601907
NM_000218.2(KCNQ1):c.19C>T (p.Pro7Ser) rs199473443
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_000218.2(KCNQ1):c.458C>T (p.Thr153Met) rs143709408
NM_000218.2(KCNQ1):c.484G>A (p.Val162Met) rs199472692
NM_000218.2(KCNQ1):c.574C>T (p.Arg192Cys)
NM_000218.2(KCNQ1):c.820A>G (p.Ile274Val) rs199472728
NM_000218.2(KCNQ1):c.860C>A (p.Ala287Glu) rs199472735
NM_000218.2(KCNQ1):c.868G>A (p.Glu290Lys) rs199473464

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