Slc11a1 Variant Search Result - Rat Genome Database

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94 records found for search term Slc11a1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405267919	CV3202643	single nucleotide variant	NM_000578.4(SLC11A1):c.796-4G>A	SLC11A1-related disorder [RCV003911863]	likely benign	2	218389866	218389866	Human		name , trait , alternate_id
405290286	CV3214158	single nucleotide variant	NM_000578.4(SLC11A1):c.796-5C>T	SLC11A1-related disorder [RCV003926990]	likely benign	2	218389865	218389865	Human		name , trait , alternate_id
15182377	CV730108	single nucleotide variant	NM_000578.4(SLC11A1):c.571+8C>T	not provided [RCV000885977]	likely benign	2	218387238	218387238	Human		name
15165591	CV777234	single nucleotide variant	NM_000578.4(SLC11A1):c.501-4T>G	not provided [RCV000948627]	benign	2	218387156	218387156	Human		name
15195185	CV730109	single nucleotide variant	NM_000578.4(SLC11A1):c.1165-7A>C	not provided [RCV000889432]	benign	2	218392974	218392974	Human		name
15199035	CV759138	single nucleotide variant	NM_000578.4(SLC11A1):c.1045-7C>T	not provided [RCV000912429]	likely benign	2	218391369	218391369	Human		name
405265556	CV3185740	single nucleotide variant	NM_000578.4(SLC11A1):c.36G>A (p.Gly12=)	not provided [RCV003886304]	likely benign	2	218382988	218382988	Human		name
8560964	CV24271	single nucleotide variant	NM_000578.4(SLC11A1):c.198C>T (p.Phe66=)	Mycobacterium tuberculosis, susceptibility to infection by [RCV000009813]	risk factor	2	218384290	218384290	Human	1	name
405278403	CV3221862	single nucleotide variant	NM_000578.4(SLC11A1):c.115C>T (p.Leu39=)	SLC11A1-related disorder [RCV003976423]	benign	2	218383067	218383067	Human		name , trait , alternate_id
156343700	CV2349224	single nucleotide variant	NM_000578.4(SLC11A1):c.71C>T (p.Pro24Leu)	not specified [RCV004199177]	uncertain significance	2	218383023	218383023	Human		name
155962641	CV2388268	single nucleotide variant	NM_000578.4(SLC11A1):c.62C>T (p.Pro21Leu)	not specified [RCV004234725]	uncertain significance	2	218383014	218383014	Human		name
401721579	CV2683569	single nucleotide variant	NM_000578.4(SLC11A1):c.34G>A (p.Gly12Arg)	not specified [RCV004282500]	likely benign	2	218382986	218382986	Human		name
405285582	CV3206511	single nucleotide variant	NM_000578.4(SLC11A1):c.747C>T (p.Gly249=)	SLC11A1-related disorder [RCV003981221]	benign	2	218387907	218387907	Human		name , trait , alternate_id
405290292	CV3214159	single nucleotide variant	NM_000578.4(SLC11A1):c.870C>T (p.Ile290=)	SLC11A1-related disorder [RCV003926991]	likely benign	2	218389944	218389944	Human		name , trait , alternate_id
597740092	CV3599359	single nucleotide variant	NM_000578.4(SLC11A1):c.80C>T (p.Pro27Leu)	not specified [RCV004864597]	uncertain significance	2	218383032	218383032	Human		name
15131577	CV708029	single nucleotide variant	NM_000578.4(SLC11A1):c.522C>T (p.Val174=)	not provided [RCV000964625]	benign	2	218387181	218387181	Human		name
15120659	CV762917	single nucleotide variant	NM_000578.4(SLC11A1):c.324A>T (p.Arg108=)	not provided [RCV000940384]	likely benign	2	218385197	218385197	Human		name
156384616	CV2231134	single nucleotide variant	NM_000578.4(SLC11A1):c.296C>T (p.Ala99Val)	not specified [RCV004094349]	uncertain significance	2	218385169	218385169	Human		name
156085888	CV2249366	single nucleotide variant	NM_000578.4(SLC11A1):c.149C>T (p.Pro50Leu)	not specified [RCV004118378]	uncertain significance	2	218383101	218383101	Human		name
156276140	CV2316513	single nucleotide variant	NM_000578.4(SLC11A1):c.155C>T (p.Thr52Ile)	not specified [RCV004169982]	uncertain significance	2	218384247	218384247	Human		name
401768099	CV2727381	single nucleotide variant	NM_000578.4(SLC11A1):c.220G>C (p.Asp74His)	not specified [RCV004327480]	uncertain significance	2	218384312	218384312	Human		name
405274481	CV3208788	single nucleotide variant	NM_000578.4(SLC11A1):c.1143C>T (p.Tyr381=)	SLC11A1-related disorder [RCV003951595]	likely benign	2	218391474	218391474	Human		name , trait , alternate_id
405766316	CV3332466	single nucleotide variant	NM_000578.4(SLC11A1):c.143C>T (p.Thr48Ile)	not specified [RCV004456198]	uncertain significance	2	218383095	218383095	Human		name
405766321	CV3332467	single nucleotide variant	NM_000578.4(SLC11A1):c.256G>A (p.Ala86Thr)	not specified [RCV004456199]	uncertain significance	2	218384348	218384348	Human		name
407502724	CV3477071	single nucleotide variant	NM_000578.4(SLC11A1):c.203T>A (p.Met68Lys)	not specified [RCV004670046]	uncertain significance	2	218384295	218384295	Human		name
597740102	CV3599361	single nucleotide variant	NM_000578.4(SLC11A1):c.166C>T (p.Arg56Trp)	not specified [RCV004864599]	uncertain significance	2	218384258	218384258	Human		name
598267495	CV3911057	single nucleotide variant	NM_000578.4(SLC11A1):c.191C>T (p.Pro64Leu)	not specified [RCV005281591]	uncertain significance	2	218384283	218384283	Human		name
15197797	CV747290	single nucleotide variant	NM_000578.4(SLC11A1):c.1255C>A (p.Arg419=)	not provided [RCV000912075]	likely benign	2	218393071	218393071	Human		name
126912082	CV1037146	single nucleotide variant	NM_000578.4(SLC11A1):c.811C>T (p.Arg271Trp)	not provided [RCV001356121]\|not specified [RCV004034455]	uncertain significance	2	218389885	218389885	Human		name
126910291	CV1037147	single nucleotide variant	NM_000578.4(SLC11A1):c.943A>C (p.Asn315His)	not provided [RCV001354501]	uncertain significance	2	218390017	218390017	Human		name
155979336	CV2215175	single nucleotide variant	NM_000578.4(SLC11A1):c.545T>C (p.Phe182Ser)	not specified [RCV004086892]	uncertain significance	2	218387204	218387204	Human		name
156145049	CV2265022	single nucleotide variant	NM_000578.4(SLC11A1):c.824C>G (p.Ala275Gly)	not specified [RCV004126182]	uncertain significance	2	218389898	218389898	Human		name
156243623	CV2267275	single nucleotide variant	NM_000578.4(SLC11A1):c.862G>A (p.Ala288Thr)	not specified [RCV004133950]	uncertain significance	2	218389936	218389936	Human		name
156346016	CV2309005	single nucleotide variant	NM_000578.4(SLC11A1):c.558C>G (p.Phe186Leu)	not specified [RCV004171068]	uncertain significance	2	218387217	218387217	Human		name
156222882	CV2344004	single nucleotide variant	NM_000578.4(SLC11A1):c.821G>A (p.Arg274Gln)	not specified [RCV004195621]	uncertain significance	2	218389895	218389895	Human		name
156114657	CV2349223	single nucleotide variant	NM_000578.4(SLC11A1):c.505C>A (p.Pro169Thr)	not specified [RCV004199176]	uncertain significance	2	218387164	218387164	Human		name
156198047	CV2357792	single nucleotide variant	NM_000578.4(SLC11A1):c.908T>C (p.Met303Thr)	not specified [RCV004205081]	uncertain significance	2	218389982	218389982	Human		name
156133682	CV2361905	single nucleotide variant	NM_000578.4(SLC11A1):c.473T>C (p.Ile158Thr)	not specified [RCV004207678]	uncertain significance	2	218386714	218386714	Human		name
156267475	CV2371801	single nucleotide variant	NM_000578.4(SLC11A1):c.812G>A (p.Arg271Gln)	not specified [RCV004603382]	uncertain significance	2	218389886	218389886	Human		name
156144332	CV2383922	single nucleotide variant	NM_000578.4(SLC11A1):c.984C>A (p.His328Gln)	not provided [RCV005256899]\|not specified [RCV004231774]	likely benign\|uncertain significance	2	218391227	218391227	Human		name
329353815	CV2439728	single nucleotide variant	NM_000578.4(SLC11A1):c.433A>T (p.Ile145Phe)	not specified [RCV004255736]	uncertain significance	2	218386674	218386674	Human		name
329399952	CV2444416	single nucleotide variant	NM_000578.4(SLC11A1):c.644T>C (p.Val215Ala)	not specified [RCV004263158]	uncertain significance	2	218387804	218387804	Human		name
329391431	CV2448550	single nucleotide variant	NM_000578.4(SLC11A1):c.406G>A (p.Val136Ile)	not specified [RCV004259230]	uncertain significance	2	218386647	218386647	Human		name
329377882	CV2460804	single nucleotide variant	NM_000578.4(SLC11A1):c.660G>C (p.Glu220Asp)	not specified [RCV004271123]	likely benign	2	218387820	218387820	Human		name
401751677	CV2672539	single nucleotide variant	NM_000578.4(SLC11A1):c.731C>T (p.Ala244Val)	not specified [RCV004287576]	uncertain significance	2	218387891	218387891	Human		name
401734314	CV2688468	single nucleotide variant	NM_000578.4(SLC11A1):c.658G>C (p.Glu220Gln)	not specified [RCV004301447]	uncertain significance	2	218387818	218387818	Human		name
401734456	CV2690593	single nucleotide variant	NM_000578.4(SLC11A1):c.367G>A (p.Glu123Lys)	not specified [RCV004304686]	uncertain significance	2	218385240	218385240	Human		name
401870368	CV2765912	single nucleotide variant	NM_000578.4(SLC11A1):c.878C>T (p.Ser293Phe)	not specified [RCV004337940]	uncertain significance	2	218389952	218389952	Human		name
405266971	CV3202086	single nucleotide variant	NM_000578.4(SLC11A1):c.875T>C (p.Leu292Pro)	SLC11A1-related disorder [RCV003911566]	likely benign	2	218389949	218389949	Human		name , trait , alternate_id
405766330	CV3332468	single nucleotide variant	NM_000578.4(SLC11A1):c.307G>T (p.Gly103Cys)	not specified [RCV004456200]	uncertain significance	2	218385180	218385180	Human		name
405766336	CV3332469	single nucleotide variant	NM_000578.4(SLC11A1):c.373T>A (p.Cys125Ser)	not specified [RCV004456201]	uncertain significance	2	218385246	218385246	Human		name
405766341	CV3332470	single nucleotide variant	NM_000578.4(SLC11A1):c.445G>A (p.Asp149Asn)	not specified [RCV004456202]	uncertain significance	2	218386686	218386686	Human		name
405766352	CV3332472	single nucleotide variant	NM_000578.4(SLC11A1):c.972C>G (p.Asn324Lys)	not specified [RCV004456204]	uncertain significance	2	218391215	218391215	Human		name
407502721	CV3477070	single nucleotide variant	NM_000578.4(SLC11A1):c.382T>C (p.Tyr128His)	not specified [RCV004670045]	uncertain significance	2	218385255	218385255	Human		name
407502734	CV3477074	single nucleotide variant	NM_000578.4(SLC11A1):c.586G>C (p.Glu196Gln)	not specified [RCV004670049]	uncertain significance	2	218387579	218387579	Human		name
597740057	CV3599353	single nucleotide variant	NM_000578.4(SLC11A1):c.687C>A (p.Phe229Leu)	not specified [RCV004864591]	likely benign	2	218387847	218387847	Human		name
597740063	CV3599354	single nucleotide variant	NM_000578.4(SLC11A1):c.824C>T (p.Ala275Val)	not specified [RCV004864592]	likely benign	2	218389898	218389898	Human		name
597740076	CV3599356	single nucleotide variant	NM_000578.4(SLC11A1):c.453G>C (p.Gln151His)	not specified [RCV004864594]	uncertain significance	2	218386694	218386694	Human		name
597740097	CV3599360	single nucleotide variant	NM_000578.4(SLC11A1):c.334C>A (p.Arg112Ser)	not specified [RCV004864598]	uncertain significance	2	218385207	218385207	Human		name
597740114	CV3599363	single nucleotide variant	NM_000578.4(SLC11A1):c.643G>C (p.Val215Leu)	not specified [RCV004864601]	uncertain significance	2	218387803	218387803	Human		name
14702721	CV626125	single nucleotide variant	NM_000578.4(SLC11A1):c.806T>C (p.Ile269Thr)	Mycobacterium tuberculosis, susceptibility to [RCV000791139]	uncertain significance	2	218389880	218389880	Human	1	name
156120428	CV2219350	single nucleotide variant	NM_000578.4(SLC11A1):c.1114G>A (p.Gly372Arg)	not specified [RCV004095191]	uncertain significance	2	218391445	218391445	Human		name
156184420	CV2222502	single nucleotide variant	NM_000578.4(SLC11A1):c.1052T>C (p.Ile351Thr)	not specified [RCV004099347]	uncertain significance	2	218391383	218391383	Human		name
156386218	CV2228148	single nucleotide variant	NM_000578.4(SLC11A1):c.1075G>A (p.Ala359Thr)	not specified [RCV004096364]	uncertain significance	2	218391406	218391406	Human		name
156300448	CV2244912	single nucleotide variant	NM_000578.4(SLC11A1):c.1194C>G (p.Phe398Leu)	not specified [RCV004104662]	uncertain significance	2	218393010	218393010	Human		name
156346748	CV2305479	single nucleotide variant	NM_000578.4(SLC11A1):c.1199G>A (p.Arg400His)	not specified [RCV004165194]	uncertain significance	2	218393015	218393015	Human		name
156273892	CV2320218	single nucleotide variant	NM_000578.4(SLC11A1):c.1499C>T (p.Ala500Val)	not specified [RCV004169838]	likely benign	2	218394742	218394742	Human		name
156105259	CV2352519	single nucleotide variant	NM_000578.4(SLC11A1):c.1327G>A (p.Val443Met)	not specified [RCV004203021]	uncertain significance	2	218394132	218394132	Human		name
156223571	CV2400052	single nucleotide variant	NM_000578.4(SLC11A1):c.1382A>G (p.Asn461Ser)	not specified [RCV004246968]	uncertain significance	2	218394187	218394187	Human		name
156195837	CV2400548	single nucleotide variant	NM_000578.4(SLC11A1):c.1567G>A (p.Gly523Arg)	not specified [RCV004246738]	uncertain significance	2	218394949	218394949	Human		name
8560965	CV24272	single nucleotide variant	NM_000578.4(SLC11A1):c.1627G>A (p.Asp543Asn)	Buruli ulcer, susceptibility to [RCV000009814]\|Cystic fibrosis [RCV005357103]	risk factor\|uncertain significance	2	218395009	218395009	Human	2	name
329358918	CV2450751	single nucleotide variant	NM_000578.4(SLC11A1):c.1283A>G (p.Asn428Ser)	not specified [RCV004267684]	uncertain significance	2	218393099	218393099	Human		name
329393065	CV2469267	single nucleotide variant	NM_000578.4(SLC11A1):c.1265G>A (p.Arg422Lys)	not specified [RCV004280607]	uncertain significance	2	218393081	218393081	Human		name
329352770	CV2470449	single nucleotide variant	NM_000578.4(SLC11A1):c.1325C>T (p.Ala442Val)	not specified [RCV004273476]	uncertain significance	2	218394130	218394130	Human		name
401736628	CV2688838	single nucleotide variant	NM_000578.4(SLC11A1):c.1432G>A (p.Ala478Thr)	not specified [RCV004303854]	uncertain significance	2	218394675	218394675	Human		name
401770802	CV2726265	single nucleotide variant	NM_000578.4(SLC11A1):c.1487A>G (p.Tyr496Cys)	not specified [RCV004326715]	uncertain significance	2	218394730	218394730	Human		name
401757618	CV2731350	single nucleotide variant	NM_000578.4(SLC11A1):c.1155C>G (p.Phe385Leu)	not specified [RCV004330719]	uncertain significance	2	218391486	218391486	Human		name
401859876	CV2768376	single nucleotide variant	NM_000578.4(SLC11A1):c.1645T>C (p.Ser549Pro)	not specified [RCV004350629]	uncertain significance	2	218395027	218395027	Human		name
401864576	CV2781868	single nucleotide variant	NM_000578.4(SLC11A1):c.1214G>T (p.Arg405Leu)	not specified [RCV004356812]	uncertain significance	2	218393030	218393030	Human		name
405265391	CV3199098	single nucleotide variant	NM_000578.4(SLC11A1):c.1256G>A (p.Arg419Gln)	SLC11A1-related disorder [RCV003897400]	benign	2	218393072	218393072	Human		name , trait , alternate_id
405766296	CV3332463	single nucleotide variant	NM_000578.4(SLC11A1):c.1190G>A (p.Arg397His)	not specified [RCV004456195]	uncertain significance	2	218393006	218393006	Human		name
405766302	CV3332464	single nucleotide variant	NM_000578.4(SLC11A1):c.1319C>T (p.Pro440Leu)	not specified [RCV004456196]	uncertain significance	2	218394124	218394124	Human		name
405871887	CV3398122	single nucleotide variant	NM_000578.4(SLC11A1):c.1450G>C (p.Val484Leu)	not provided [RCV004575123]	benign	2	218394693	218394693	Human		name
407502731	CV3477073	single nucleotide variant	NM_000578.4(SLC11A1):c.1139C>T (p.Thr380Ile)	not specified [RCV004670048]	uncertain significance	2	218391470	218391470	Human		name
407519412	CV3477075	single nucleotide variant	NM_000578.4(SLC11A1):c.1267G>A (p.Asp423Asn)	not specified [RCV004676495]	uncertain significance	2	218393083	218393083	Human		name
597740080	CV3599357	single nucleotide variant	NM_000578.4(SLC11A1):c.1605C>G (p.Phe535Leu)	not specified [RCV004864595]	uncertain significance	2	218394987	218394987	Human		name
597740084	CV3599358	single nucleotide variant	NM_000578.4(SLC11A1):c.1370A>G (p.Gln457Arg)	not specified [RCV004864596]	uncertain significance	2	218394175	218394175	Human		name
597740109	CV3599362	single nucleotide variant	NM_000578.4(SLC11A1):c.1513G>A (p.Ala505Thr)	not specified [RCV004864600]	likely benign	2	218394756	218394756	Human		name
598199788	CV3911056	single nucleotide variant	NM_000578.4(SLC11A1):c.1450G>A (p.Val484Met)	not specified [RCV005268447]	uncertain significance	2	218394693	218394693	Human		name
598267502	CV3911058	single nucleotide variant	NM_000578.4(SLC11A1):c.1145C>T (p.Ala382Val)	not specified [RCV005281592]	uncertain significance	2	218391476	218391476	Human		name
598267508	CV3911059	single nucleotide variant	NM_000578.4(SLC11A1):c.1361C>G (p.Thr454Ser)	not specified [RCV005281593]	uncertain significance	2	218394166	218394166	Human		name
15157654	CV708030	single nucleotide variant	NM_000578.4(SLC11A1):c.1328T>C (p.Val443Ala)	not provided [RCV000969348]	benign	2	218394133	218394133	Human		name
15138471	CV733163	single nucleotide variant	NM_000578.4(SLC11A1):c.1048G>A (p.Val350Met)	not provided [RCV000898987]	likely benign	2	218391379	218391379	Human		name
15178192	CV733164	single nucleotide variant	NM_000578.4(SLC11A1):c.1492G>A (p.Gly498Ser)	SLC11A1-related disorder [RCV003910844]\|not provided [RCV000906819]	benign	2	218394735	218394735	Human	1	name , trait , alternate_id

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