ClinVar Miner

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

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Gene type:
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Total variants: 85
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HGVS dbSNP
NC_000009.12:g.135702113A>T
NC_000009.12:g.135759397del
NC_000009.12:g.135766057_135766070del
NM_020822.3(KCNT1):c.1035+292C>T
NM_020822.3(KCNT1):c.1036-170A>G
NM_020822.3(KCNT1):c.1036-206G>A
NM_020822.3(KCNT1):c.1036-207C>T
NM_020822.3(KCNT1):c.1036-233C>T
NM_020822.3(KCNT1):c.1036-39A>G
NM_020822.3(KCNT1):c.1036-94T>C
NM_020822.3(KCNT1):c.1200+130T>C
NM_020822.3(KCNT1):c.1200+177_1200+196del
NM_020822.3(KCNT1):c.1337+121A>C
NM_020822.3(KCNT1):c.1337+198T>C
NM_020822.3(KCNT1):c.1337+29A>G
NM_020822.3(KCNT1):c.1337+81G>A
NM_020822.3(KCNT1):c.1338-219G>A
NM_020822.3(KCNT1):c.1338-56G>A
NM_020822.3(KCNT1):c.1401+29G>A
NM_020822.3(KCNT1):c.1402-64C>T
NM_020822.3(KCNT1):c.1422C>T (p.Arg474=) rs372250372
NM_020822.3(KCNT1):c.1510+163T>C
NM_020822.3(KCNT1):c.1510+163_1510+202del
NM_020822.3(KCNT1):c.1510+183_1510+222del
NM_020822.3(KCNT1):c.1510+206_1510+245del
NM_020822.3(KCNT1):c.1510+265A>G
NM_020822.3(KCNT1):c.1510+307T>C
NM_020822.3(KCNT1):c.1510+321C>T
NM_020822.3(KCNT1):c.1510+96A>G
NM_020822.3(KCNT1):c.1619+38C>T
NM_020822.3(KCNT1):c.1619+45G>A
NM_020822.3(KCNT1):c.1769+172G>T
NM_020822.3(KCNT1):c.1769+67T>G
NM_020822.3(KCNT1):c.1770-42G>A
NM_020822.3(KCNT1):c.2008+114T>C
NM_020822.3(KCNT1):c.2008+115G>A
NM_020822.3(KCNT1):c.2008+215G>A
NM_020822.3(KCNT1):c.2008+21G>A
NM_020822.3(KCNT1):c.2008+238A>G
NM_020822.3(KCNT1):c.2009-206G>A
NM_020822.3(KCNT1):c.2009-222G>A
NM_020822.3(KCNT1):c.2166G>A (p.Leu722=) rs374347802
NM_020822.3(KCNT1):c.2243+277A>T
NM_020822.3(KCNT1):c.2243+56G>A
NM_020822.3(KCNT1):c.2244-184G>A
NM_020822.3(KCNT1):c.2244-217T>C
NM_020822.3(KCNT1):c.2244-309T>C
NM_020822.3(KCNT1):c.2244-327C>T
NM_020822.3(KCNT1):c.2349+148A>G
NM_020822.3(KCNT1):c.2349+269C>T
NM_020822.3(KCNT1):c.2349+301G>A
NM_020822.3(KCNT1):c.2349+319C>A
NM_020822.3(KCNT1):c.2349+325_2349+326insA
NM_020822.3(KCNT1):c.2349+326G>T
NM_020822.3(KCNT1):c.2349+59T>C
NM_020822.3(KCNT1):c.2349+7C>T rs190849453
NM_020822.3(KCNT1):c.2350-109A>G
NM_020822.3(KCNT1):c.2427G>A (p.Thr809=) rs914428
NM_020822.3(KCNT1):c.2523-294C>A
NM_020822.3(KCNT1):c.255-164A>G
NM_020822.3(KCNT1):c.255-294G>A
NM_020822.3(KCNT1):c.255-295C>T
NM_020822.3(KCNT1):c.2595-83C>G
NM_020822.3(KCNT1):c.2729+31A>G
NM_020822.3(KCNT1):c.2729G>A (p.Arg910Gln) rs151272083
NM_020822.3(KCNT1):c.2730-164_2730-98del
NM_020822.3(KCNT1):c.2841+212G>A
NM_020822.3(KCNT1):c.2842-69A>C
NM_020822.3(KCNT1):c.2842-80C>G
NM_020822.3(KCNT1):c.3177+67A>T
NM_020822.3(KCNT1):c.3387C>T (p.Ala1129=) rs372410150
NM_020822.3(KCNT1):c.3503-68T>C
NM_020822.3(KCNT1):c.3587+63T>C
NM_020822.3(KCNT1):c.3587+71C>T
NM_020822.3(KCNT1):c.3690C>T (p.Arg1230=) rs141521745
NM_020822.3(KCNT1):c.434+25C>A
NM_020822.3(KCNT1):c.434+269G>A
NM_020822.3(KCNT1):c.435-257G>C
NM_020822.3(KCNT1):c.435-67C>T
NM_020822.3(KCNT1):c.492-86C>T
NM_020822.3(KCNT1):c.541-225C>T
NM_020822.3(KCNT1):c.760-110_760-109insACAGGTGTGGCCAGGTGCAGGCTGCCCCATGGGCCTCAGCCGAGACACAGGTGTGGCCAGGTGTAGGCTGCCCCGTGGGCCTCAGCCGAGAC
NM_020822.3(KCNT1):c.760-139A>G
NM_020822.3(KCNT1):c.855-43A>G
NM_020822.3(KCNT1):c.942C>T (p.Thr314=) rs144766991

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