Dctd Variant Search Result - Rat Genome Database

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20 records found for search term Dctd

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15196737	CV698448	single nucleotide variant	NM_001921.3(DCTD):c.255G>C (p.Ala85=)	not provided [RCV000956270]	benign	4	182894595	182894595	Human		name
156295619	CV2233748	single nucleotide variant	NM_001921.3(DCTD):c.68C>G (p.Ala23Gly)	not specified [RCV004100191]	uncertain significance	4	182915501	182915501	Human		name
405702409	CV3243388	single nucleotide variant	NM_001921.3(DCTD):c.72C>G (p.Phe24Leu)	not specified [RCV004375444]	uncertain significance	4	182915497	182915497	Human		name
156043907	CV2237562	single nucleotide variant	NM_001921.3(DCTD):c.291T>A (p.Asp97Glu)	not specified [RCV004106502]	uncertain significance	4	182894559	182894559	Human		name
156155851	CV2266171	single nucleotide variant	NM_001921.3(DCTD):c.181A>T (p.Ser61Cys)	not specified [RCV004128751]	uncertain significance	4	182914986	182914986	Human		name
401883303	CV2785639	single nucleotide variant	NM_001921.3(DCTD):c.148G>T (p.Gly50Trp)	not specified [RCV004363140]	uncertain significance	4	182915019	182915019	Human		name
405702393	CV3243386	single nucleotide variant	NM_001921.3(DCTD):c.124G>A (p.Val42Met)	not specified [RCV004375442]	uncertain significance	4	182915043	182915043	Human		name
407458257	CV3430396	single nucleotide variant	NM_001921.3(DCTD):c.227A>T (p.Asp76Val)	not specified [RCV004611497]	uncertain significance	4	182914940	182914940	Human		name
598262695	CV3959848	single nucleotide variant	NM_001921.3(DCTD):c.196C>T (p.Pro66Ser)	not specified [RCV005325455]	uncertain significance	4	182914971	182914971	Human		name
156328058	CV2219998	single nucleotide variant	NM_001921.3(DCTD):c.497T>G (p.Phe166Cys)	not specified [RCV004095591]	uncertain significance	4	182891439	182891439	Human		name
156041677	CV2310910	single nucleotide variant	NM_001921.3(DCTD):c.409G>A (p.Glu137Lys)	not specified [RCV004163949]	uncertain significance	4	182893080	182893080	Human		name
156136509	CV2364968	single nucleotide variant	NM_001921.3(DCTD):c.528G>C (p.Lys176Asn)	not specified [RCV004222261]	uncertain significance	4	182891408	182891408	Human		name
401890214	CV2758857	single nucleotide variant	NM_001921.3(DCTD):c.518C>T (p.Pro173Leu)	not specified [RCV004339947]	uncertain significance	4	182891418	182891418	Human		name
405702402	CV3243387	single nucleotide variant	NM_001921.3(DCTD):c.448G>T (p.Val150Leu)	not specified [RCV004375443]	uncertain significance	4	182893041	182893041	Human		name
407458259	CV3430397	single nucleotide variant	NM_001921.3(DCTD):c.398A>G (p.His133Arg)	not specified [RCV004611498]	uncertain significance	4	182893091	182893091	Human		name
597783350	CV3661803	single nucleotide variant	NM_001921.3(DCTD):c.448G>A (p.Val150Met)	not specified [RCV004900166]	uncertain significance	4	182893041	182893041	Human		name
597801143	CV3661804	single nucleotide variant	NM_001921.3(DCTD):c.344A>C (p.Lys115Thr)	not specified [RCV004906055]	uncertain significance	4	182894506	182894506	Human		name
598262683	CV3959845	single nucleotide variant	NM_001921.3(DCTD):c.470C>A (p.Pro157Gln)	not specified [RCV005325452]	uncertain significance	4	182891466	182891466	Human		name
598262688	CV3959846	single nucleotide variant	NM_001921.3(DCTD):c.478A>G (p.Ser160Gly)	not specified [RCV005325453]	uncertain significance	4	182891458	182891458	Human		name
598262691	CV3959847	single nucleotide variant	NM_001921.3(DCTD):c.482A>G (p.Lys161Arg)	not specified [RCV005325454]	uncertain significance	4	182891454	182891454	Human		name

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