Kctd4 Variant Search Result - Rat Genome Database

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18 records found for search term Kctd4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156299198	CV2244712	single nucleotide variant	NM_198404.3(KCTD4):c.29A>G (p.Lys10Arg)	not specified [RCV004102712]	uncertain significance	13	45194539	45194539	Human		name
597796846	CV3694979	single nucleotide variant	NM_198404.3(KCTD4):c.46G>A (p.Gly16Arg)	not specified [RCV004935603]	uncertain significance	13	45194522	45194522	Human		name
156099118	CV2294609	single nucleotide variant	NM_198404.3(KCTD4):c.209C>T (p.Pro70Leu)	not specified [RCV004161867]	uncertain significance	13	45194359	45194359	Human		name
405812437	CV3265203	single nucleotide variant	NM_198404.3(KCTD4):c.268C>G (p.Leu90Val)	not specified [RCV004408944]	uncertain significance	13	45194300	45194300	Human		name
156101386	CV2260334	single nucleotide variant	NM_198404.3(KCTD4):c.449A>T (p.Asp150Val)	not specified [RCV004129420]	uncertain significance	13	45194119	45194119	Human		name
156158135	CV2398005	single nucleotide variant	NM_198404.3(KCTD4):c.578T>C (p.Ile193Thr)	not specified [RCV004241607]	uncertain significance	13	45193990	45193990	Human		name
156003801	CV2400921	single nucleotide variant	NM_198404.3(KCTD4):c.659T>G (p.Leu220Trp)	not specified [RCV004244211]	uncertain significance	13	45193909	45193909	Human		name
329369744	CV2424899	single nucleotide variant	NM_198404.3(KCTD4):c.746T>C (p.Ile249Thr)	not specified [RCV004248780]	uncertain significance	13	45193822	45193822	Human		name
401890198	CV2763693	single nucleotide variant	NM_198404.3(KCTD4):c.487G>C (p.Asp163His)	not specified [RCV004343193]	uncertain significance	13	45194081	45194081	Human		name
405812439	CV3265204	single nucleotide variant	NM_198404.3(KCTD4):c.511C>T (p.Arg171Cys)	not specified [RCV004408945]	uncertain significance	13	45194057	45194057	Human		name
405812441	CV3265205	single nucleotide variant	NM_198404.3(KCTD4):c.512G>A (p.Arg171His)	not specified [RCV004408946]	uncertain significance	13	45194056	45194056	Human		name
597796838	CV3694974	single nucleotide variant	NM_198404.3(KCTD4):c.520C>A (p.Leu174Met)	not specified [RCV004935600]	uncertain significance	13	45194048	45194048	Human		name
597767342	CV3694976	single nucleotide variant	NM_198404.3(KCTD4):c.580A>G (p.Ile194Val)	not specified [RCV004927265]	uncertain significance	13	45193988	45193988	Human		name
597796841	CV3694977	single nucleotide variant	NM_198404.3(KCTD4):c.478A>G (p.Asn160Asp)	not specified [RCV004935601]	uncertain significance	13	45194090	45194090	Human		name
597796843	CV3694978	single nucleotide variant	NM_198404.3(KCTD4):c.493A>G (p.Ile165Val)	not specified [RCV004935602]	uncertain significance	13	45194075	45194075	Human		name
597796849	CV3694980	single nucleotide variant	NM_198404.3(KCTD4):c.386G>A (p.Arg129Lys)	not specified [RCV004935604]	uncertain significance	13	45194182	45194182	Human		name
598236026	CV3976452	single nucleotide variant	NM_198404.3(KCTD4):c.314G>A (p.Arg105Gln)	not specified [RCV005363768]	uncertain significance	13	45194254	45194254	Human		name
598270371	CV3976453	single nucleotide variant	NM_198404.3(KCTD4):c.672G>C (p.Lys224Asn)	not specified [RCV005350090]	uncertain significance	13	45193896	45193896	Human		name