ClinVar Miner

List of variants in gene KCNQ1 reported as likely benign by Color

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Total variants: 21
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HGVS dbSNP
NM_181798.1(KCNQ1):c.1134-3C>T rs1564886312
NM_181798.1(KCNQ1):c.1215G>A (p.Ala405=) rs558452873
NM_181798.1(KCNQ1):c.1227C>T (p.Tyr409=) rs138551008
NM_181798.1(KCNQ1):c.1368C>T (p.Arg456=) rs200670744
NM_181798.1(KCNQ1):c.1386C>T (p.Gly462=) rs368364062
NM_181798.1(KCNQ1):c.1419G>A (p.Thr473=) rs147091980
NM_181798.1(KCNQ1):c.1545C>T (p.Cys515=) rs12720454
NM_181798.1(KCNQ1):c.222C>T (p.Ile74=) rs146190510
NM_181798.1(KCNQ1):c.291G>A (p.Thr97=) rs550887954
NM_181798.1(KCNQ1):c.342C>T (p.Val114=) rs1358413257
NM_181798.1(KCNQ1):c.423C>T (p.Ile141=) rs373227792
NM_181798.1(KCNQ1):c.558C>T (p.Ile186=) rs199472747
NM_181798.1(KCNQ1):c.603C>T (p.Ile201=) rs140019543
NM_181798.1(KCNQ1):c.652-4C>T rs543599445
NM_181798.1(KCNQ1):c.747+6G>A rs558595162
NM_181798.1(KCNQ1):c.78G>A (p.Thr26=) rs148121889
NM_181798.1(KCNQ1):c.798G>T (p.Lys266Asn) rs12720457
NM_181798.1(KCNQ1):c.871-3del rs12720450
NM_181798.1(KCNQ1):c.900A>G (p.Lys300=) rs763197403
NM_181798.1(KCNQ1):c.993C>T (p.Val331=) rs778598703
NM_181798.1(KCNQ1):c.996C>T (p.Asp332=) rs200418488

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