Slc38a11 Variant Search Result - Rat Genome Database

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42 records found for search term Slc38a11

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15155813	CV778894	duplication	NM_001351537.2(SLC38A11):c.689-10dup	not provided [RCV000968992]	benign	2	164915282	164915283	Human		name
155929449	CV2356840	single nucleotide variant	NM_001351537.2(SLC38A11):c.262G>T (p.Ala88Ser)	not specified [RCV004202177]	uncertain significance	2	164945695	164945695	Human		name
405708585	CV3329044	single nucleotide variant	NM_001351537.2(SLC38A11):c.259G>A (p.Gly87Arg)	not specified [RCV004461432]	uncertain significance	2	164945698	164945698	Human		name
598243506	CV3914931	single nucleotide variant	NM_001351537.2(SLC38A11):c.201G>T (p.Leu67Phe)	not specified [RCV005276717]	uncertain significance	2	164952735	164952735	Human		name
156335610	CV2228417	single nucleotide variant	NM_001351537.2(SLC38A11):c.814A>G (p.Thr272Ala)	not specified [RCV004098393]	uncertain significance	2	164915148	164915148	Human		name
156231726	CV2245107	single nucleotide variant	NM_001351537.2(SLC38A11):c.709T>G (p.Ser237Ala)	not specified [RCV004106908]	uncertain significance	2	164915253	164915253	Human		name
156219152	CV2254017	single nucleotide variant	NM_001351537.2(SLC38A11):c.721T>G (p.Tyr241Asp)	not specified [RCV004129473]	uncertain significance	2	164915241	164915241	Human		name
155967964	CV2277097	single nucleotide variant	NM_001351537.2(SLC38A11):c.302A>G (p.Lys101Arg)	not specified [RCV004142748]	uncertain significance	2	164945655	164945655	Human		name
155918222	CV2332958	single nucleotide variant	NM_001351537.2(SLC38A11):c.553A>G (p.Thr185Ala)	not specified [RCV004194259]	uncertain significance	2	164937414	164937414	Human		name
155913770	CV2341854	single nucleotide variant	NM_001351537.2(SLC38A11):c.515G>A (p.Arg172Gln)	not specified [RCV004184805]	uncertain significance	2	164939472	164939472	Human		name
156072258	CV2376821	single nucleotide variant	NM_001351537.2(SLC38A11):c.937C>T (p.Pro313Ser)	not specified [RCV004227481]	uncertain significance	2	164911662	164911662	Human		name
156347778	CV2382975	single nucleotide variant	NM_001351537.2(SLC38A11):c.929T>G (p.Leu310Trp)	not specified [RCV004217562]	uncertain significance	2	164911670	164911670	Human		name
156392934	CV2385469	single nucleotide variant	NM_001351537.2(SLC38A11):c.807C>G (p.Phe269Leu)	not specified [RCV004233117]	likely benign	2	164915155	164915155	Human		name
329373989	CV2434660	single nucleotide variant	NM_001351537.2(SLC38A11):c.478T>C (p.Ser160Pro)	not specified [RCV004248380]	uncertain significance	2	164939509	164939509	Human		name
401745289	CV2681235	single nucleotide variant	NM_001351537.2(SLC38A11):c.884A>T (p.Asp295Val)	not specified [RCV004289372]	uncertain significance	2	164911715	164911715	Human		name
401735340	CV2699242	single nucleotide variant	NM_001351537.2(SLC38A11):c.673G>A (p.Gly225Arg)	not specified [RCV004305518]	uncertain significance	2	164915918	164915918	Human		name
401868387	CV2781775	single nucleotide variant	NM_001351537.2(SLC38A11):c.781G>A (p.Val261Met)	not specified [RCV004356738]	uncertain significance	2	164915181	164915181	Human		name
405708545	CV3329038	single nucleotide variant	NM_001351537.2(SLC38A11):c.448T>A (p.Phe150Ile)	not specified [RCV004461426]	uncertain significance	2	164939539	164939539	Human		name
405708551	CV3329039	single nucleotide variant	NM_001351537.2(SLC38A11):c.461A>G (p.His154Arg)	not specified [RCV004461427]	uncertain significance	2	164939526	164939526	Human		name
405708556	CV3329040	single nucleotide variant	NM_001351537.2(SLC38A11):c.479C>A (p.Ser160Tyr)	not specified [RCV004461428]	uncertain significance	2	164939508	164939508	Human		name
405708562	CV3329041	single nucleotide variant	NM_001351537.2(SLC38A11):c.803T>C (p.Ile268Thr)	not specified [RCV004461429]	uncertain significance	2	164915159	164915159	Human		name
405708573	CV3329042	single nucleotide variant	NM_001351537.2(SLC38A11):c.961G>C (p.Glu321Gln)	not specified [RCV004461430]	uncertain significance	2	164911638	164911638	Human		name
407451625	CV3484544	single nucleotide variant	NM_001351537.2(SLC38A11):c.860T>C (p.Phe287Ser)	not specified [RCV004683723]	uncertain significance	2	164911739	164911739	Human		name
597703054	CV3599889	single nucleotide variant	NM_001351537.2(SLC38A11):c.434A>G (p.Asp145Gly)	not specified [RCV004860157]	uncertain significance	2	164939553	164939553	Human		name
597703065	CV3599891	single nucleotide variant	NM_001351537.2(SLC38A11):c.940A>G (p.Met314Val)	not specified [RCV004860158]	uncertain significance	2	164911659	164911659	Human		name
598243486	CV3914927	single nucleotide variant	NM_001351537.2(SLC38A11):c.760C>T (p.Arg254Cys)	not specified [RCV005276714]	uncertain significance	2	164915202	164915202	Human		name
598237184	CV3914928	single nucleotide variant	NM_001351537.2(SLC38A11):c.992A>C (p.Asn331Thr)	not specified [RCV005275607]	uncertain significance	2	164908743	164908743	Human		name
598243493	CV3914929	single nucleotide variant	NM_001351537.2(SLC38A11):c.824A>G (p.Tyr275Cys)	not specified [RCV005276715]	uncertain significance	2	164915138	164915138	Human		name
598243513	CV3914932	single nucleotide variant	NM_001351537.2(SLC38A11):c.941T>C (p.Met314Thr)	not specified [RCV005276718]	uncertain significance	2	164911658	164911658	Human		name
598243520	CV3914933	single nucleotide variant	NM_001351537.2(SLC38A11):c.683C>A (p.Ser228Tyr)	not specified [RCV005276719]	uncertain significance	2	164915908	164915908	Human		name
598243527	CV3914935	single nucleotide variant	NM_001351537.2(SLC38A11):c.722A>G (p.Tyr241Cys)	not specified [RCV005276720]	uncertain significance	2	164915240	164915240	Human		name
156163665	CV2323621	single nucleotide variant	NM_001351537.2(SLC38A11):c.1363A>C (p.Thr455Pro)	not specified [RCV004165810]	uncertain significance	2	164898463	164898463	Human		name
329383240	CV2434476	single nucleotide variant	NM_001351537.2(SLC38A11):c.1360T>C (p.Ser454Pro)	not specified [RCV004254185]	uncertain significance	2	164898466	164898466	Human		name
329351956	CV2455526	single nucleotide variant	NM_001351537.2(SLC38A11):c.1075G>A (p.Gly359Arg)	not specified [RCV004276788]	uncertain significance	2	164908660	164908660	Human		name
401864021	CV2767466	single nucleotide variant	NM_001351537.2(SLC38A11):c.1355A>C (p.Gln452Pro)	not specified [RCV004343630]	uncertain significance	2	164898471	164898471	Human		name
405708534	CV3329037	single nucleotide variant	NM_001351537.2(SLC38A11):c.1216G>T (p.Ala406Ser)	not specified [RCV004461425]	uncertain significance	2	164898610	164898610	Human		name
405708580	CV3329043	single nucleotide variant	NM_001351537.2(SLC38A11):c.1076G>A (p.Gly359Glu)	not specified [RCV004461431]	uncertain significance	2	164908659	164908659	Human		name
405708589	CV3329045	single nucleotide variant	NM_001351537.2(SLC38A11):c.1127T>C (p.Ile376Thr)	not specified [RCV004461433]	uncertain significance	2	164898699	164898699	Human		name
407514656	CV3484543	single nucleotide variant	NM_001351537.2(SLC38A11):c.1178C>T (p.Ser393Phe)	not specified [RCV004674653]	uncertain significance	2	164898648	164898648	Human		name
597765692	CV3599888	single nucleotide variant	NM_001351537.2(SLC38A11):c.1276G>T (p.Gly426Trp)	not specified [RCV004870470]	uncertain significance	2	164898550	164898550	Human		name
597765695	CV3599890	single nucleotide variant	NM_001351537.2(SLC38A11):c.1046C>T (p.Thr349Met)	not specified [RCV004870471]	uncertain significance	2	164908689	164908689	Human		name
598243500	CV3914930	single nucleotide variant	NM_001351537.2(SLC38A11):c.1121T>C (p.Ile374Thr)	not specified [RCV005276716]	uncertain significance	2	164898705	164898705	Human		name

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