Kcnn1 Variant Search Result - Rat Genome Database

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42 records found for search term Kcnn1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15188997	CV745052	single nucleotide variant	NM_001386974.1(KCNN1):c.917+8C>T	not provided [RCV000909525]	benign	19	17982135	17982135	Human		name
15173041	CV741711	single nucleotide variant	NM_001386974.1(KCNN1):c.90C>T (p.Ala30=)	not provided [RCV000905788]	benign	19	17973978	17973978	Human		name
156118797	CV2279152	single nucleotide variant	NM_001386974.1(KCNN1):c.64G>A (p.Gly22Arg)	not specified [RCV004139391]	uncertain significance	19	17973952	17973952	Human		name
401937124	CV2811826	single nucleotide variant	NM_001386974.1(KCNN1):c.765C>T (p.Ala255=)	not provided [RCV003415145]	likely benign	19	17981975	17981975	Human		name
155925994	CV2258667	single nucleotide variant	NM_001386974.1(KCNN1):c.169G>A (p.Gly57Ser)	not specified [RCV004117914]	uncertain significance	19	17974057	17974057	Human		name
156285606	CV2360819	single nucleotide variant	NM_001386974.1(KCNN1):c.158G>A (p.Arg53Gln)	not specified [RCV004213594]	likely benign	19	17974046	17974046	Human		name
156034405	CV2376675	single nucleotide variant	NM_001386974.1(KCNN1):c.140C>G (p.Ala47Gly)	not specified [RCV004222872]	uncertain significance	19	17974028	17974028	Human		name
156268445	CV2398436	single nucleotide variant	NM_001386974.1(KCNN1):c.101C>T (p.Pro34Leu)	not specified [RCV004237764]	uncertain significance	19	17973989	17973989	Human		name
405806997	CV3264985	single nucleotide variant	NM_001386974.1(KCNN1):c.110C>T (p.Pro37Leu)	not specified [RCV004406333]	uncertain significance	19	17973998	17973998	Human		name
405807002	CV3264987	single nucleotide variant	NM_001386974.1(KCNN1):c.119C>T (p.Pro40Leu)	not specified [RCV004406335]	uncertain significance	19	17974007	17974007	Human		name
405807008	CV3264990	single nucleotide variant	NM_001386974.1(KCNN1):c.179G>A (p.Arg60Gln)	not specified [RCV004406338]	uncertain significance	19	17974067	17974067	Human		name
598235484	CV3976243	single nucleotide variant	NM_001386974.1(KCNN1):c.116G>A (p.Ser39Asn)	not specified [RCV005363672]	uncertain significance	19	17974004	17974004	Human		name
156005023	CV2357619	single nucleotide variant	NM_001386974.1(KCNN1):c.355G>A (p.Val119Ile)	not specified [RCV004202881]	uncertain significance	19	17974243	17974243	Human		name
329373139	CV2455906	single nucleotide variant	NM_001386974.1(KCNN1):c.484G>A (p.Ala162Thr)	not specified [RCV004279178]	uncertain significance	19	17975173	17975173	Human		name
401740524	CV2681445	single nucleotide variant	NM_001386974.1(KCNN1):c.355G>T (p.Val119Phe)	not specified [RCV004291985]	uncertain significance	19	17974243	17974243	Human		name
401759600	CV2701628	single nucleotide variant	NM_001386974.1(KCNN1):c.904C>T (p.Arg302Cys)	not specified [RCV004314047]	uncertain significance	19	17982114	17982114	Human		name
597796392	CV3694728	single nucleotide variant	NM_001386974.1(KCNN1):c.479A>G (p.Tyr160Cys)	not specified [RCV004935456]	uncertain significance	19	17975168	17975168	Human		name
597796396	CV3694729	single nucleotide variant	NM_001386974.1(KCNN1):c.448A>G (p.Thr150Ala)	not specified [RCV004935457]	uncertain significance	19	17975137	17975137	Human		name
598235477	CV3976242	single nucleotide variant	NM_001386974.1(KCNN1):c.653C>T (p.Ala218Val)	not specified [RCV005363671]	uncertain significance	19	17981863	17981863	Human		name
598213112	CV3976244	single nucleotide variant	NM_001386974.1(KCNN1):c.907G>A (p.Val303Ile)	not specified [RCV005358932]	uncertain significance	19	17982117	17982117	Human		name
598235496	CV3976246	single nucleotide variant	NM_001386974.1(KCNN1):c.692C>G (p.Ser231Cys)	not specified [RCV005363674]	uncertain significance	19	17981902	17981902	Human		name
156256203	CV2219738	single nucleotide variant	NM_001386974.1(KCNN1):c.1078C>T (p.Leu360Phe)	not specified [RCV004095436]	uncertain significance	19	17988433	17988433	Human		name
155945541	CV2238000	single nucleotide variant	NM_001386974.1(KCNN1):c.1598G>A (p.Arg533Gln)	not specified [RCV004111034]	uncertain significance	19	17998372	17998372	Human		name
155967551	CV2329934	single nucleotide variant	NM_001386974.1(KCNN1):c.1034G>T (p.Gly345Val)	not specified [RCV004183388]	uncertain significance	19	17985428	17985428	Human		name
155952918	CV2393863	single nucleotide variant	NM_001386974.1(KCNN1):c.1366G>A (p.Asp456Asn)	not specified [RCV004233687]	uncertain significance	19	17993548	17993548	Human		name
329369176	CV2450555	single nucleotide variant	NM_001386974.1(KCNN1):c.1430A>T (p.Glu477Val)	not specified [RCV004265460]	uncertain significance	19	17998204	17998204	Human		name
401741339	CV2680600	single nucleotide variant	NM_001386974.1(KCNN1):c.1472C>T (p.Ala491Val)	not specified [RCV004291223]	uncertain significance	19	17998246	17998246	Human		name
401734870	CV2688638	single nucleotide variant	NM_001386974.1(KCNN1):c.1132G>A (p.Val378Met)	not specified [RCV004301586]	uncertain significance	19	17988487	17988487	Human		name
401746675	CV2690946	single nucleotide variant	NM_001386974.1(KCNN1):c.1223A>T (p.His408Leu)	not specified [RCV004300971]	uncertain significance	19	17989768	17989768	Human		name
401746670	CV2694903	single nucleotide variant	NM_001386974.1(KCNN1):c.1099C>T (p.Arg367Trp)	not specified [RCV004300970]	uncertain significance	19	17988454	17988454	Human		name
401762883	CV2707314	single nucleotide variant	NM_001386974.1(KCNN1):c.1442G>A (p.Arg481His)	not specified [RCV004312719]	uncertain significance	19	17998216	17998216	Human		name
401777698	CV2718306	single nucleotide variant	NM_001386974.1(KCNN1):c.1619C>T (p.Ser540Leu)	not specified [RCV004318144]	uncertain significance	19	17998393	17998393	Human		name
401863507	CV2765862	single nucleotide variant	NM_001386974.1(KCNN1):c.1252G>T (p.Ala418Ser)	not specified [RCV004337899]	uncertain significance	19	17989797	17989797	Human		name
405806999	CV3264986	single nucleotide variant	NM_001386974.1(KCNN1):c.1169G>A (p.Arg390Gln)	not specified [RCV004406334]	uncertain significance	19	17988524	17988524	Human		name
405807006	CV3264989	single nucleotide variant	NM_001386974.1(KCNN1):c.1565C>G (p.Pro522Arg)	not specified [RCV004406337]	uncertain significance	19	17998339	17998339	Human		name
407516500	CV3445134	single nucleotide variant	NM_001386974.1(KCNN1):c.1230G>C (p.Arg410Ser)	not specified [RCV004628217]	uncertain significance	19	17989775	17989775	Human		name
407516503	CV3445135	single nucleotide variant	NM_001386974.1(KCNN1):c.1253C>T (p.Ala418Val)	not specified [RCV004628218]	uncertain significance	19	17989798	17989798	Human		name
597796382	CV3694725	single nucleotide variant	NM_001386974.1(KCNN1):c.1597C>T (p.Arg533Trp)	not specified [RCV004935453]	uncertain significance	19	17998371	17998371	Human		name
597796387	CV3694726	single nucleotide variant	NM_001386974.1(KCNN1):c.1522C>T (p.Arg508Cys)	not specified [RCV004935454]	uncertain significance	19	17998296	17998296	Human		name
597796389	CV3694727	single nucleotide variant	NM_001386974.1(KCNN1):c.1583G>A (p.Arg528Gln)	not specified [RCV004935455]	uncertain significance	19	17998357	17998357	Human		name
598235470	CV3976240	single nucleotide variant	NM_001386974.1(KCNN1):c.1561G>A (p.Gly521Ser)	not specified [RCV005363670]	uncertain significance	19	17998335	17998335	Human		name
598235489	CV3976245	single nucleotide variant	NM_001386974.1(KCNN1):c.1600T>C (p.Trp534Arg)	not specified [RCV005363673]	uncertain significance	19	17998374	17998374	Human		name

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