ClinVar Miner

List of variants reported for Long QT syndrome 10 by Fulgent Genetics, Fulgent Genetics

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Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_174934.4(SCN4B):c.639C>T (p.Asn213=) rs72544155 0.00341
NM_174934.4(SCN4B):c.*961A>G rs561492722 0.00058
NM_174934.4(SCN4B):c.*2977A>G rs369720674 0.00041
NM_174934.4(SCN4B):c.*2196G>A rs769472607 0.00031
NM_174934.4(SCN4B):c.520A>G (p.Ile174Val) rs377730779 0.00019
NM_174934.4(SCN4B):c.*670G>T rs182613927 0.00016
NM_174934.4(SCN4B):c.617C>T (p.Ser206Leu) rs140348243 0.00010
NM_174934.4(SCN4B):c.347T>C (p.Ile116Thr) rs769406938 0.00004
NM_174934.4(SCN4B):c.482C>G (p.Thr161Arg) rs750329453 0.00003
NM_174934.4(SCN4B):c.115A>G (p.Thr39Ala) rs756210130 0.00001
NM_174934.4(SCN4B):c.21A>G (p.Gly7=) rs1332884912 0.00001
NM_174934.4(SCN4B):c.40T>G (p.Trp14Gly) rs946169910 0.00001
NM_174934.4(SCN4B):c.454G>A (p.Val152Ile) rs778247172 0.00001
NM_174934.4(SCN4B):c.649G>T (p.Gly217Cys) rs371609756 0.00001
NM_174934.4(SCN4B):c.*1410C>T rs886047722
NM_174934.4(SCN4B):c.234+1G>A rs1341627207
NM_174934.4(SCN4B):c.632C>G (p.Thr211Arg) rs201454653

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