Nrn1 Variant Search Result - Rat Genome Database

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26 records found for search term Nrn1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598264762	CV3998133	single nucleotide variant	NM_016588.3(NRN1):c.19G>C (p.Gly7Arg)	not specified [RCV005387822]	uncertain significance	6	6006731	6006731	Human		name
15175650	CV722089	single nucleotide variant	NM_016588.3(NRN1):c.19G>A (p.Gly7Ser)	not provided [RCV000884417]	benign	6	6006731	6006731	Human		name
156198835	CV2237481	single nucleotide variant	NM_016588.3(NRN1):c.94G>A (p.Asp32Asn)	not specified [RCV004106438]	uncertain significance	6	6002459	6002459	Human		name
598220412	CV3998131	single nucleotide variant	NM_016588.3(NRN1):c.88A>G (p.Lys30Glu)	not specified [RCV005379503]	uncertain significance	6	6002465	6002465	Human		name
598264756	CV3998132	single nucleotide variant	NM_016588.3(NRN1):c.65T>C (p.Val22Ala)	not specified [RCV005387821]	uncertain significance	6	6002488	6002488	Human		name
156151350	CV2268946	single nucleotide variant	NM_016588.3(NRN1):c.397T>C (p.Ser133Pro)	not specified [RCV004128350]	uncertain significance	6	5999008	5999008	Human		name
155992431	CV2286198	single nucleotide variant	NM_016588.3(NRN1):c.334G>A (p.Gly112Ser)	not specified [RCV004146164]	uncertain significance	6	5999071	5999071	Human		name
155925055	CV2348276	single nucleotide variant	NM_016588.3(NRN1):c.375C>G (p.Phe125Leu)	not specified [RCV004191312]	likely benign	6	5999030	5999030	Human		name
401767946	CV2735082	single nucleotide variant	NM_016588.3(NRN1):c.373T>C (p.Phe125Leu)	not specified [RCV004332999]	likely benign	6	5999032	5999032	Human		name
401729101	CV2735083	single nucleotide variant	NM_016588.3(NRN1):c.391T>G (p.Ser131Ala)	not specified [RCV004333000]	uncertain significance	6	5999014	5999014	Human		name
597643074	CV3576880	single nucleotide variant	NM_016588.3(NRN1):c.424T>C (p.Phe142Leu)	not specified [RCV004832549]	uncertain significance	6	5998981	5998981	Human		name
401743283	CV2715443	single nucleotide variant	NM_198443.2(NRN1L):c.43C>T (p.Pro15Ser)	not specified [RCV004324759]	uncertain significance	16	67884946	67884946	Human		name
401761532	CV2726805	single nucleotide variant	NM_198443.2(NRN1L):c.163C>T (p.Arg55Cys)	not specified [RCV004323113]	uncertain significance	16	67885805	67885805	Human		name
401861822	CV2756734	single nucleotide variant	NM_198443.2(NRN1L):c.134T>C (p.Ile45Thr)	not specified [RCV004345241]	uncertain significance	16	67885776	67885776	Human		name
401875431	CV2766053	single nucleotide variant	NM_198443.2(NRN1L):c.110C>T (p.Ala37Val)	not specified [RCV004340512]	likely benign	16	67885752	67885752	Human		name
405709233	CV3359249	single nucleotide variant	NM_198443.2(NRN1L):c.193G>A (p.Glu65Lys)	not specified [RCV004493596]	uncertain significance	16	67885835	67885835	Human		name
407516940	CV3465918	single nucleotide variant	NM_198443.2(NRN1L):c.184C>T (p.Arg62Cys)	not specified [RCV004650460]	uncertain significance	16	67885826	67885826	Human		name
598220419	CV3998134	single nucleotide variant	NM_198443.2(NRN1L):c.185G>A (p.Arg62His)	not specified [RCV005379504]	likely benign	16	67885827	67885827	Human		name
155943284	CV2298499	single nucleotide variant	NM_198443.2(NRN1L):c.466G>A (p.Ala156Thr)	not specified [RCV004162163]	uncertain significance	16	67886227	67886227	Human		name
155970231	CV2338041	single nucleotide variant	NM_198443.2(NRN1L):c.365G>A (p.Arg122Gln)	not specified [RCV004186081]	likely benign	16	67886126	67886126	Human		name
156077086	CV2375082	single nucleotide variant	NM_198443.2(NRN1L):c.370C>T (p.Arg124Cys)	not specified [RCV004230130]	uncertain significance	16	67886131	67886131	Human		name
155971054	CV2392429	single nucleotide variant	NM_198443.2(NRN1L):c.485G>A (p.Arg162Lys)	not specified [RCV004244009]	uncertain significance	16	67886246	67886246	Human		name
405709241	CV3359250	single nucleotide variant	NM_198443.2(NRN1L):c.323C>T (p.Pro108Leu)	not specified [RCV004493597]	uncertain significance	16	67886084	67886084	Human		name
13820827	CV576174	single nucleotide variant	NM_198443.2(NRN1L):c.345C>A (p.Cys115Ter)	not provided [RCV000709906]	not provided	16	67886106	67886106	Human		name
15161642	CV703779	single nucleotide variant	NM_198443.2(NRN1L):c.323C>G (p.Pro108Arg)	not provided [RCV000947709]	benign	16	67886084	67886084	Human		name
15174680	CV740304	single nucleotide variant	NM_198443.2(NRN1L):c.445C>T (p.Pro149Ser)	not provided [RCV000906025]	benign	16	67886206	67886206	Human		name

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