ClinVar Miner

List of variants in gene KCNT1 reported as benign by GeneDx

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Total variants: 37
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HGVS dbSNP
NM_020822.2(KCNT1):c.1008C>T (p.Cys336=) rs540422455
NM_020822.2(KCNT1):c.1036-15G>A rs112341167
NM_020822.2(KCNT1):c.1056C>G (p.Leu352=) rs116691849
NM_020822.2(KCNT1):c.116C>T (p.Pro39Leu) rs201051863
NM_020822.2(KCNT1):c.1200+12T>G rs58604946
NM_020822.2(KCNT1):c.1533G>A (p.Glu511=) rs151080601
NM_020822.2(KCNT1):c.1628A>G (p.Gln543Arg) rs200173000
NM_020822.2(KCNT1):c.1879A>G (p.Ile627Val) rs143355299
NM_020822.2(KCNT1):c.2142G>A (p.Leu714=) rs370580872
NM_020822.2(KCNT1):c.2210C>T (p.Thr737Met) rs61744696
NM_020822.2(KCNT1):c.2235C>T (p.Ser745=) rs146810749
NM_020822.2(KCNT1):c.2349+7C>T rs190849453
NM_020822.2(KCNT1):c.2376C>T (p.Asp792=) rs149028586
NM_020822.2(KCNT1):c.2427G>A (p.Thr809=) rs914428
NM_020822.2(KCNT1):c.2430C>T (p.Ala810=) rs139114208
NM_020822.2(KCNT1):c.254+18_254+19dupGG rs141291153
NM_020822.2(KCNT1):c.254+20T>C rs2385007
NM_020822.2(KCNT1):c.2619C>T (p.Gly873=) rs144659358
NM_020822.2(KCNT1):c.2729+9A>G rs12005420
NM_020822.2(KCNT1):c.2892C>T (p.Phe964=) rs146904895
NM_020822.2(KCNT1):c.2943+6C>T rs28612938
NM_020822.2(KCNT1):c.30G>A (p.Pro10=) rs139034501
NM_020822.2(KCNT1):c.3256G>A (p.Gly1086Arg) rs201156458
NM_020822.2(KCNT1):c.3295C>T (p.Pro1099Ser) rs200642629
NM_020822.2(KCNT1):c.3312G>A (p.Leu1104=) rs149416418
NM_020822.2(KCNT1):c.333G>A (p.Ser111=) rs56008253
NM_020822.2(KCNT1):c.3388G>A (p.Ala1130Thr) rs138421850
NM_020822.2(KCNT1):c.3390G>A (p.Ala1130=) rs77912754
NM_020822.2(KCNT1):c.3502+16G>A rs112116686
NM_020822.2(KCNT1):c.3690C>T (p.Arg1230=) rs141521745
NM_020822.2(KCNT1):c.435-17G>A rs140115987
NM_020822.2(KCNT1):c.59G>C (p.Gly20Ala) rs146292575
NM_020822.2(KCNT1):c.600+11G>A rs375220600
NM_020822.2(KCNT1):c.711C>G (p.Pro237=) rs117286274
NM_020822.2(KCNT1):c.978A>G (p.Pro326=) rs61739517
NM_020822.2(KCNT1):c.985C>T (p.Leu329=) rs147165522
NM_020822.2(KCNT1):c.99A>G (p.Gln33=) rs146152956

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