Mif Variant Search Result - Rat Genome Database

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40 records found for search term Mif

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405287748	CV3217939	single nucleotide variant	NM_002415.2(MIF):c.282-6C>G	MIF-related disorder [RCV003982062]	benign	22	23895034	23895034	Human		name , trait , alternate_id
15176749	CV731405	single nucleotide variant	NM_002415.2(MIF):c.282-7C>A	not provided [RCV000884652]	benign	22	23895033	23895033	Human		name
15123299	CV780160	single nucleotide variant	NM_002415.2(MIF):c.282-9C>T	not provided [RCV000963214]	benign	22	23895031	23895031	Human		name
401921893	CV2822039	single nucleotide variant	NM_002415.2(MIF):c.5C>G (p.Pro2Arg)	not provided [RCV003433179]	uncertain significance	22	23894479	23894479	Human		name
405268850	CV3199111	single nucleotide variant	NM_002415.2(MIF):c.204C>A (p.Ile68=)	MIF-related disorder [RCV003912215]	likely benign	22	23894867	23894867	Human		name , trait , alternate_id
156238822	CV2193668	single nucleotide variant	NM_002415.2(MIF):c.83C>T (p.Ala28Val)	not specified [RCV004074265]	uncertain significance	22	23894557	23894557	Human		name
156035659	CV2376784	single nucleotide variant	NM_002415.2(MIF):c.100C>A (p.Pro34Thr)	not specified [RCV004227062]	uncertain significance	22	23894574	23894574	Human		name
401720272	CV2705797	single nucleotide variant	NM_002415.2(MIF):c.221G>T (p.Arg74Leu)	not specified [RCV004318629]	uncertain significance	22	23894884	23894884	Human		name
401757721	CV2707929	single nucleotide variant	NM_002415.2(MIF):c.142A>G (p.Met48Val)	not specified [RCV004309194]	uncertain significance	22	23894805	23894805	Human		name
401890091	CV2763637	single nucleotide variant	NM_002415.2(MIF):c.195C>G (p.Ile65Met)	not specified [RCV004343143]	uncertain significance	22	23894858	23894858	Human		name
405288986	CV3204905	single nucleotide variant	NM_002415.2(MIF):c.224C>T (p.Ser75Phe)	MIF-related disorder [RCV003961552]	likely benign	22	23894887	23894887	Human		name , trait , alternate_id
405672615	CV3285701	single nucleotide variant	NM_002415.2(MIF):c.220C>G (p.Arg74Gly)	not specified [RCV004419850]	uncertain significance	22	23894883	23894883	Human		name
597646671	CV3560358	single nucleotide variant	NM_002415.2(MIF):c.142A>C (p.Met48Leu)	not specified [RCV004833096]	uncertain significance	22	23894805	23894805	Human		name
597646687	CV3560360	single nucleotide variant	NM_002415.2(MIF):c.154G>T (p.Gly52Cys)	not specified [RCV004833098]	uncertain significance	22	23894817	23894817	Human		name
13706276	CV537400	single nucleotide variant	NM_002415.2(MIF):c.172G>A (p.Ala58Thr)	not provided [RCV000658931]	uncertain significance	22	23894835	23894835	Human		name
597646680	CV3560359	single nucleotide variant	NM_002415.2(MIF):c.320T>A (p.Val107Glu)	not specified [RCV004833097]	uncertain significance	22	23895078	23895078	Human		name
156237601	CV2224220	single nucleotide variant	NM_001370592.1(MIF4GD):c.82+717A>G	not specified [RCV004096058]	uncertain significance	17	75269397	75269397	Human		name
156264638	CV2364353	single nucleotide variant	NM_001370592.1(MIF4GD):c.82+731C>T	not specified [RCV004223571]	uncertain significance	17	75269383	75269383	Human		name
597635846	CV3560367	single nucleotide variant	NM_001370592.1(MIF4GD):c.82+689G>C	not specified [RCV004824447]	uncertain significance	17	75269425	75269425	Human		name
598254459	CV3993191	single nucleotide variant	NM_001370592.1(MIF4GD):c.82+756C>T	not specified [RCV005367204]	uncertain significance	17	75269358	75269358	Human		name
155905686	CV2393761	single nucleotide variant	NM_001370592.1(MIF4GD):c.21G>C (p.Glu7Asp)	not specified [RCV004233599]	uncertain significance	17	75270175	75270175	Human		name
401765005	CV2701698	single nucleotide variant	NM_001370592.1(MIF4GD):c.80A>T (p.Lys27Ile)	not specified [RCV004314106]	uncertain significance	17	75270116	75270116	Human		name
156281714	CV2338481	single nucleotide variant	NM_001370592.1(MIF4GD):c.255G>T (p.Gln85His)	not specified [RCV004188521]	uncertain significance	17	75267839	75267839	Human		name
401726829	CV2674562	single nucleotide variant	NM_001370592.1(MIF4GD):c.169C>T (p.Arg57Cys)	not specified [RCV004291439]	uncertain significance	17	75268106	75268106	Human		name
401865688	CV2786094	single nucleotide variant	NM_001370592.1(MIF4GD):c.105G>C (p.Glu35Asp)	not specified [RCV004359906]	uncertain significance	17	75268170	75268170	Human		name
405672619	CV3285702	single nucleotide variant	NM_001370592.1(MIF4GD):c.230G>A (p.Arg77His)	not specified [RCV004419851]	uncertain significance	17	75267864	75267864	Human		name
597646714	CV3560365	single nucleotide variant	NM_001370592.1(MIF4GD):c.245G>A (p.Arg82Gln)	not specified [RCV004833102]	uncertain significance	17	75267849	75267849	Human		name
598186441	CV3993192	single nucleotide variant	NM_001370592.1(MIF4GD):c.221T>G (p.Val74Gly)	not specified [RCV005373406]	uncertain significance	17	75267873	75267873	Human		name
156245034	CV2283397	single nucleotide variant	NM_001370592.1(MIF4GD):c.430A>G (p.Lys144Glu)	not specified [RCV004139626]	uncertain significance	17	75267549	75267549	Human		name
155905933	CV2303212	single nucleotide variant	NM_001370592.1(MIF4GD):c.658G>A (p.Val220Ile)	not specified [RCV004156971]	uncertain significance	17	75266751	75266751	Human		name
401755850	CV2675540	single nucleotide variant	NM_001370592.1(MIF4GD):c.508A>G (p.Met170Val)	not specified [RCV004295156]	uncertain significance	17	75266901	75266901	Human		name
401881644	CV2784758	single nucleotide variant	NM_001370592.1(MIF4GD):c.397C>T (p.Leu133Phe)	not specified [RCV004352554]	uncertain significance	17	75267582	75267582	Human		name
405672623	CV3285703	single nucleotide variant	NM_001370592.1(MIF4GD):c.298G>C (p.Gly100Arg)	not specified [RCV004419852]	uncertain significance	17	75267796	75267796	Human		name
407518506	CV3447016	single nucleotide variant	NM_001370592.1(MIF4GD):c.404G>A (p.Arg135Gln)	not specified [RCV004628897]	uncertain significance	17	75267575	75267575	Human		name
597646693	CV3560361	single nucleotide variant	NM_001370592.1(MIF4GD):c.596T>C (p.Ile199Thr)	not specified [RCV004833099]	uncertain significance	17	75266813	75266813	Human		name
597646699	CV3560363	single nucleotide variant	NM_001370592.1(MIF4GD):c.613G>A (p.Gly205Ser)	not specified [RCV004833100]	uncertain significance	17	75266796	75266796	Human		name
597646708	CV3560364	single nucleotide variant	NM_001370592.1(MIF4GD):c.603C>G (p.Phe201Leu)	not specified [RCV004833101]	uncertain significance	17	75266806	75266806	Human		name
597646722	CV3560366	single nucleotide variant	NM_001370592.1(MIF4GD):c.664G>A (p.Asp222Asn)	not specified [RCV004833103]	uncertain significance	17	75266745	75266745	Human		name
598186435	CV3993190	single nucleotide variant	NM_001370592.1(MIF4GD):c.472G>A (p.Val158Ile)	not specified [RCV005373405]	uncertain significance	17	75266937	75266937	Human		name
598254467	CV3993195	single nucleotide variant	NM_001370592.1(MIF4GD):c.341A>G (p.Tyr114Cys)	not specified [RCV005367205]	uncertain significance	17	75267753	75267753	Human		name

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