ClinVar Miner

List of variants in gene KCNT1 reported as likely benign for not provided

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Total variants: 60
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HGVS dbSNP
NC_000009.12:g.135769943G>A
NC_000009.12:g.135770455C>T
NC_000009.12:g.135777298_135777309del
NC_000009.12:g.135777328C>T
NC_000009.12:g.135786187_135786196dup
NM_020822.3(KCNT1):c.-40C>T
NM_020822.3(KCNT1):c.1036-160G>T
NM_020822.3(KCNT1):c.1036-168C>G
NM_020822.3(KCNT1):c.1036-205G>T
NM_020822.3(KCNT1):c.110+154G>A
NM_020822.3(KCNT1):c.1156C>T (p.Leu386Phe) rs780875110
NM_020822.3(KCNT1):c.1200+68A>G
NM_020822.3(KCNT1):c.123G>C (p.Ala41=)
NM_020822.3(KCNT1):c.1510+183T>A
NM_020822.3(KCNT1):c.1510+251C>T
NM_020822.3(KCNT1):c.1510+270A>G
NM_020822.3(KCNT1):c.1510+80C>T
NM_020822.3(KCNT1):c.1542C>T (p.Tyr514=)
NM_020822.3(KCNT1):c.1718G>A (p.Arg573His) rs575162600
NM_020822.3(KCNT1):c.1769+98G>A
NM_020822.3(KCNT1):c.1770-116C>A
NM_020822.3(KCNT1):c.1770-20T>C
NM_020822.3(KCNT1):c.1770-34G>T
NM_020822.3(KCNT1):c.1779G>A (p.Val593=)
NM_020822.3(KCNT1):c.1962C>T (p.His654=)
NM_020822.3(KCNT1):c.2009-39G>A
NM_020822.3(KCNT1):c.2030A>G (p.Gln677Arg) rs1060505000
NM_020822.3(KCNT1):c.2076C>T (p.Gly692=)
NM_020822.3(KCNT1):c.2146C>T (p.Leu716=)
NM_020822.3(KCNT1):c.2223C>T (p.Asp741=) rs144118960
NM_020822.3(KCNT1):c.2243+172C>T
NM_020822.3(KCNT1):c.2243+328G>A
NM_020822.3(KCNT1):c.2350-189G>A
NM_020822.3(KCNT1):c.2451C>T (p.Phe817=) rs942926305
NM_020822.3(KCNT1):c.2523-99C>A
NM_020822.3(KCNT1):c.2543A>G (p.Glu848Gly) rs149804567
NM_020822.3(KCNT1):c.2943+6C>T rs28612938
NM_020822.3(KCNT1):c.2944-19T>C rs759060806
NM_020822.3(KCNT1):c.2944-75C>T
NM_020822.3(KCNT1):c.299G>A (p.Arg100Gln) rs752032951
NM_020822.3(KCNT1):c.3177+129G>A
NM_020822.3(KCNT1):c.3196G>A (p.Val1066Met)
NM_020822.3(KCNT1):c.3239G>T (p.Gly1080Val) rs200250181
NM_020822.3(KCNT1):c.3288C>T (p.Gly1096=)
NM_020822.3(KCNT1):c.3295C>T (p.Pro1099Ser) rs200642629
NM_020822.3(KCNT1):c.3340C>T (p.Arg1114Trp) rs370085077
NM_020822.3(KCNT1):c.3360G>A (p.Ala1120=)
NM_020822.3(KCNT1):c.3383C>T (p.Ala1128Val) rs143704418
NM_020822.3(KCNT1):c.3388G>A (p.Ala1130Thr) rs138421850
NM_020822.3(KCNT1):c.3450C>T (p.Ser1150=) rs757210594
NM_020822.3(KCNT1):c.3495C>T (p.Thr1165=) rs374429090
NM_020822.3(KCNT1):c.3503-67G>A
NM_020822.3(KCNT1):c.3587+3G>A
NM_020822.3(KCNT1):c.3685A>G (p.Thr1229Ala) rs74533482
NM_020822.3(KCNT1):c.534G>C (p.Ala178=)
NM_020822.3(KCNT1):c.59G>C (p.Gly20Ala) rs146292575
NM_020822.3(KCNT1):c.601-13C>G rs202113794
NM_020822.3(KCNT1):c.760-138C>T
NM_020822.3(KCNT1):c.760-189_760-98del
NM_020822.3(KCNT1):c.760-231G>A

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