Map7d2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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86 records found for search term Map7d2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401931197	CV2821328	single nucleotide variant	NM_001168465.2(MAP7D2):c.485-6C>G	not provided [RCV003441127]	likely benign	X	20052994	20052994	Human		name
156236251	CV2346426	single nucleotide variant	NM_001168465.2(MAP7D2):c.25G>A (p.Gly9Arg)	not specified [RCV004203904]	uncertain significance	X	20116855	20116855	Human		name
598197998	CV3985276	single nucleotide variant	NM_001168465.2(MAP7D2):c.17G>T (p.Gly6Val)	not specified [RCV005375493]	uncertain significance	X	20116863	20116863	Human		name
150409768	CV1196345	single nucleotide variant	NM_001168465.2(MAP7D2):c.37C>T (p.Arg13Trp)	not provided [RCV001572785]\|not specified [RCV004039387]	uncertain significance	X	20116843	20116843	Human		name
401761906	CV2699451	single nucleotide variant	NM_001168465.2(MAP7D2):c.88C>T (p.Pro30Ser)	not specified [RCV004299672]	uncertain significance	X	20116792	20116792	Human		name
405811599	CV3285018	single nucleotide variant	NM_001168465.2(MAP7D2):c.38G>A (p.Arg13Gln)	not specified [RCV004408554]	uncertain significance	X	20116842	20116842	Human		name
405811603	CV3285020	single nucleotide variant	NM_001168465.2(MAP7D2):c.55C>G (p.Arg19Gly)	not specified [RCV004408556]	uncertain significance	X	20116825	20116825	Human		name
156272261	CV2297141	single nucleotide variant	NM_001168465.2(MAP7D2):c.124C>T (p.Pro42Ser)	not specified [RCV004151039]	uncertain significance	X	20116756	20116756	Human		name
329392251	CV2470521	single nucleotide variant	NM_001168465.2(MAP7D2):c.275A>G (p.Glu92Gly)	not specified [RCV004273535]	uncertain significance	X	20063511	20063511	Human		name
405811584	CV3285011	single nucleotide variant	NM_001168465.2(MAP7D2):c.121C>T (p.Arg41Trp)	not specified [RCV004408547]	uncertain significance	X	20116759	20116759	Human		name
597627929	CV3700360	single nucleotide variant	NM_001168465.2(MAP7D2):c.152C>T (p.Ser51Leu)	not specified [RCV004939052]	uncertain significance	X	20064784	20064784	Human		name
598198047	CV3985283	single nucleotide variant	NM_001168465.2(MAP7D2):c.170T>G (p.Leu57Trp)	not specified [RCV005375499]	uncertain significance	X	20064766	20064766	Human		name
15099729	CV706189	single nucleotide variant	NM_001168465.2(MAP7D2):c.2250C>T (p.Asp750=)	not provided [RCV000958805]	benign	X	20010875	20010875	Human		name
155991080	CV2255613	single nucleotide variant	NM_001168465.2(MAP7D2):c.830G>A (p.Gly277Asp)	not specified [RCV004120028]	uncertain significance	X	20044413	20044413	Human		name
156141319	CV2260486	single nucleotide variant	NM_001168465.2(MAP7D2):c.905G>A (p.Arg302Gln)	not specified [RCV004123276]	uncertain significance	X	20042604	20042604	Human		name
155996011	CV2278150	single nucleotide variant	NM_001168465.2(MAP7D2):c.665C>T (p.Ser222Phe)	not specified [RCV004141353]	uncertain significance	X	20050877	20050877	Human		name
329382502	CV2424410	single nucleotide variant	NM_001168465.2(MAP7D2):c.472G>A (p.Gly158Arg)	not specified [RCV004252306]	uncertain significance	X	20056692	20056692	Human		name
329401824	CV2457469	single nucleotide variant	NM_001168465.2(MAP7D2):c.946C>G (p.Leu316Val)	not specified [RCV004267288]	uncertain significance	X	20042563	20042563	Human		name
329401961	CV2467701	single nucleotide variant	NM_001168465.2(MAP7D2):c.589G>C (p.Asp197His)	not specified [RCV004281319]	uncertain significance	X	20052884	20052884	Human		name
401732480	CV2691020	single nucleotide variant	NM_001168465.2(MAP7D2):c.305G>A (p.Arg102Gln)	not specified [RCV004301035]	uncertain significance	X	20063481	20063481	Human		name
401778865	CV2705796	single nucleotide variant	NM_001168465.2(MAP7D2):c.511A>G (p.Met171Val)	not specified [RCV004318628]	uncertain significance	X	20052962	20052962	Human		name
401734636	CV2709561	single nucleotide variant	NM_001168465.2(MAP7D2):c.980A>G (p.Lys327Arg)	not specified [RCV004318793]	uncertain significance	X	20042529	20042529	Human		name
401858819	CV2774366	single nucleotide variant	NM_001168465.2(MAP7D2):c.970G>A (p.Gly324Ser)	not specified [RCV004347713]	uncertain significance	X	20042539	20042539	Human		name
405268270	CV3187005	single nucleotide variant	NM_001168465.2(MAP7D2):c.311G>A (p.Arg104Gln)	not provided [RCV003887088]	likely benign	X	20063475	20063475	Human		name
405811595	CV3285016	single nucleotide variant	NM_001168465.2(MAP7D2):c.342G>C (p.Glu114Asp)	not specified [RCV004408552]	uncertain significance	X	20063444	20063444	Human		name
405811597	CV3285017	single nucleotide variant	NM_001168465.2(MAP7D2):c.373G>C (p.Glu125Gln)	not specified [RCV004408553]	uncertain significance	X	20056791	20056791	Human		name
405811601	CV3285019	single nucleotide variant	NM_001168465.2(MAP7D2):c.467G>T (p.Gly156Val)	not specified [RCV004408555]	uncertain significance	X	20056697	20056697	Human		name
405811606	CV3285021	single nucleotide variant	NM_001168465.2(MAP7D2):c.599A>G (p.His200Arg)	not specified [RCV004408557]	uncertain significance	X	20050943	20050943	Human		name
405811608	CV3285022	single nucleotide variant	NM_001168465.2(MAP7D2):c.637T>C (p.Ser213Pro)	not specified [RCV004408558]	uncertain significance	X	20050905	20050905	Human		name
405811610	CV3285023	single nucleotide variant	NM_001168465.2(MAP7D2):c.677G>A (p.Ser226Asn)	not specified [RCV004408559]	uncertain significance	X	20050865	20050865	Human		name
405811612	CV3285024	single nucleotide variant	NM_001168465.2(MAP7D2):c.727G>A (p.Val243Ile)	not specified [RCV004408560]	uncertain significance	X	20044516	20044516	Human		name
405811614	CV3285025	single nucleotide variant	NM_001168465.2(MAP7D2):c.788G>A (p.Arg263Gln)	not specified [RCV004408561]	uncertain significance	X	20044455	20044455	Human		name
405811616	CV3285026	single nucleotide variant	NM_001168465.2(MAP7D2):c.960G>T (p.Glu320Asp)	not specified [RCV004408562]	likely benign	X	20042549	20042549	Human		name
407494261	CV3446637	single nucleotide variant	NM_001168465.2(MAP7D2):c.361C>T (p.Arg121Trp)	not specified [RCV004642951]	uncertain significance	X	20063425	20063425	Human		name
407494269	CV3446640	single nucleotide variant	NM_001168465.2(MAP7D2):c.835G>A (p.Gly279Arg)	not specified [RCV004642953]	uncertain significance	X	20044408	20044408	Human		name
407494282	CV3446643	single nucleotide variant	NM_001168465.2(MAP7D2):c.377G>A (p.Arg126Gln)	not specified [RCV004642956]	uncertain significance	X	20056787	20056787	Human		name
597627911	CV3700354	single nucleotide variant	NM_001168465.2(MAP7D2):c.619A>G (p.Met207Val)	not specified [RCV004939047]	uncertain significance	X	20050923	20050923	Human		name
597627915	CV3700355	single nucleotide variant	NM_001168465.2(MAP7D2):c.641G>A (p.Arg214Gln)	not specified [RCV004939048]	uncertain significance	X	20050901	20050901	Human		name
597627934	CV3700362	single nucleotide variant	NM_001168465.2(MAP7D2):c.661T>C (p.Ser221Pro)	not specified [RCV004939054]	uncertain significance	X	20050881	20050881	Human		name
598176398	CV3985271	single nucleotide variant	NM_001168465.2(MAP7D2):c.986C>A (p.Pro329Gln)	not specified [RCV005371406]	uncertain significance	X	20042523	20042523	Human		name
598198014	CV3985278	single nucleotide variant	NM_001168465.2(MAP7D2):c.536C>T (p.Pro179Leu)	not specified [RCV005375495]	uncertain significance	X	20052937	20052937	Human		name
598198022	CV3985280	single nucleotide variant	NM_001168465.2(MAP7D2):c.397C>T (p.Arg133Trp)	not specified [RCV005375496]	uncertain significance	X	20056767	20056767	Human		name
598198031	CV3985281	single nucleotide variant	NM_001168465.2(MAP7D2):c.401C>T (p.Ser134Phe)	not specified [RCV005375497]	uncertain significance	X	20056763	20056763	Human		name
155977010	CV2218665	single nucleotide variant	NM_001168465.2(MAP7D2):c.2101A>C (p.Ile701Leu)	not specified [RCV004090916]	uncertain significance	X	20011024	20011024	Human		name
155917706	CV2236629	single nucleotide variant	NM_001168465.2(MAP7D2):c.2138G>C (p.Gly713Ala)	not specified [RCV004110604]	uncertain significance	X	20010987	20010987	Human		name
156293857	CV2243530	single nucleotide variant	NM_001168465.2(MAP7D2):c.1211A>T (p.His404Leu)	not specified [RCV004112483]	uncertain significance	X	20025749	20025749	Human		name
156180580	CV2246056	single nucleotide variant	NM_001168465.2(MAP7D2):c.1340A>G (p.Glu447Gly)	not specified [RCV004113968]	uncertain significance	X	20025023	20025023	Human		name
156148902	CV2265311	single nucleotide variant	NM_001168465.2(MAP7D2):c.1313C>T (p.Ala438Val)	not specified [RCV004128203]	uncertain significance	X	20025050	20025050	Human		name
156279924	CV2325385	single nucleotide variant	NM_001168465.2(MAP7D2):c.1081C>T (p.Arg361Cys)	not specified [RCV004177754]	uncertain significance	X	20025879	20025879	Human		name
156190781	CV2325524	single nucleotide variant	NM_001168465.2(MAP7D2):c.2135C>T (p.Pro712Leu)	not specified [RCV004179963]	uncertain significance	X	20010990	20010990	Human		name
156062900	CV2352648	single nucleotide variant	NM_001168465.2(MAP7D2):c.1091C>A (p.Ala364Asp)	not specified [RCV004198680]	uncertain significance	X	20025869	20025869	Human		name
329358372	CV2425235	single nucleotide variant	NM_001168465.2(MAP7D2):c.2104C>G (p.Pro702Ala)	not specified [RCV004250907]	uncertain significance	X	20011021	20011021	Human		name
329356128	CV2430593	single nucleotide variant	NM_001168465.2(MAP7D2):c.1337C>G (p.Ala446Gly)	not specified [RCV004253788]	uncertain significance	X	20025026	20025026	Human		name
329384697	CV2435175	single nucleotide variant	NM_001168465.2(MAP7D2):c.1951C>T (p.Pro651Ser)	not specified [RCV004252812]	uncertain significance	X	20012470	20012470	Human		name
401724154	CV2681337	single nucleotide variant	NM_001168465.2(MAP7D2):c.1706A>G (p.Gln569Arg)	not specified [RCV004291886]	uncertain significance	X	20015266	20015266	Human		name
401754246	CV2685209	single nucleotide variant	NM_001168465.2(MAP7D2):c.1531G>A (p.Gly511Arg)	not specified [RCV004289765]	uncertain significance	X	20016207	20016207	Human		name
401754250	CV2685210	single nucleotide variant	NM_001168465.2(MAP7D2):c.1568G>A (p.Arg523Gln)	not specified [RCV004289766]	likely benign	X	20016170	20016170	Human		name
401782376	CV2686772	single nucleotide variant	NM_001168465.2(MAP7D2):c.1690C>A (p.Arg564Ser)	not specified [RCV004301957]	uncertain significance	X	20015282	20015282	Human		name
401891020	CV2778601	single nucleotide variant	NM_001168465.2(MAP7D2):c.1670G>A (p.Arg557Gln)	not specified [RCV004344250]	likely benign	X	20015302	20015302	Human		name
401885093	CV2786672	single nucleotide variant	NM_001168465.2(MAP7D2):c.2065G>A (p.Asp689Asn)	not specified [RCV004363799]	uncertain significance	X	20012356	20012356	Human		name
401931196	CV2821327	single nucleotide variant	NM_001168465.2(MAP7D2):c.1267G>A (p.Glu423Lys)	not provided [RCV003441126]	likely benign	X	20025693	20025693	Human		name
405811586	CV3285012	single nucleotide variant	NM_001168465.2(MAP7D2):c.1460G>A (p.Arg487His)	not specified [RCV004408548]	uncertain significance	X	20016278	20016278	Human		name
405811589	CV3285013	single nucleotide variant	NM_001168465.2(MAP7D2):c.1669C>G (p.Arg557Gly)	not specified [RCV004408549]	uncertain significance	X	20015303	20015303	Human		name
405811591	CV3285014	single nucleotide variant	NM_001168465.2(MAP7D2):c.1939C>G (p.Pro647Ala)	not specified [RCV004408550]	uncertain significance	X	20012482	20012482	Human		name
405811593	CV3285015	single nucleotide variant	NM_001168465.2(MAP7D2):c.2174G>A (p.Arg725Gln)	not specified [RCV004408551]	uncertain significance	X	20010951	20010951	Human		name
407469133	CV3446630	single nucleotide variant	NM_001168465.2(MAP7D2):c.2069T>A (p.Val690Glu)	not specified [RCV004636522]	uncertain significance	X	20012352	20012352	Human		name
407494245	CV3446632	single nucleotide variant	NM_001168465.2(MAP7D2):c.1501C>T (p.Arg501Trp)	not specified [RCV004642947]	uncertain significance	X	20016237	20016237	Human		name
407494249	CV3446633	single nucleotide variant	NM_001168465.2(MAP7D2):c.1691G>A (p.Arg564His)	not specified [RCV004642948]	uncertain significance	X	20015281	20015281	Human		name
407469136	CV3446634	single nucleotide variant	NM_001168465.2(MAP7D2):c.1630A>G (p.Met544Val)	not specified [RCV004636523]	uncertain significance	X	20016108	20016108	Human		name
407494253	CV3446635	single nucleotide variant	NM_001168465.2(MAP7D2):c.2155A>G (p.Asn719Asp)	not specified [RCV004642949]	uncertain significance	X	20010970	20010970	Human		name
407494257	CV3446636	single nucleotide variant	NM_001168465.2(MAP7D2):c.1082G>A (p.Arg361His)	not specified [RCV004642950]	uncertain significance	X	20025878	20025878	Human		name
407494265	CV3446638	single nucleotide variant	NM_001168465.2(MAP7D2):c.1660A>G (p.Thr554Ala)	not specified [RCV004642952]	likely benign	X	20015312	20015312	Human		name
407469139	CV3446639	single nucleotide variant	NM_001168465.2(MAP7D2):c.1142A>G (p.Asn381Ser)	not specified [RCV004636524]	uncertain significance	X	20025818	20025818	Human		name
407494272	CV3446641	single nucleotide variant	NM_001168465.2(MAP7D2):c.1061C>T (p.Pro354Leu)	not specified [RCV004642954]	uncertain significance	X	20025899	20025899	Human		name
597627919	CV3700357	single nucleotide variant	NM_001168465.2(MAP7D2):c.2219C>T (p.Pro740Leu)	not specified [RCV004939049]	uncertain significance	X	20010906	20010906	Human		name
597627922	CV3700358	single nucleotide variant	NM_001168465.2(MAP7D2):c.2108A>G (p.Glu703Gly)	not specified [RCV004939050]	uncertain significance	X	20011017	20011017	Human		name
597627925	CV3700359	single nucleotide variant	NM_001168465.2(MAP7D2):c.1609C>A (p.Gln537Lys)	not specified [RCV004939051]	likely benign	X	20016129	20016129	Human		name
597627932	CV3700361	single nucleotide variant	NM_001168465.2(MAP7D2):c.1276G>A (p.Ala426Thr)	not specified [RCV004939053]	uncertain significance	X	20025684	20025684	Human		name
598176384	CV3985269	single nucleotide variant	NM_001168465.2(MAP7D2):c.1870G>T (p.Val624Phe)	not specified [RCV005371404]	uncertain significance	X	20013069	20013069	Human		name
598176392	CV3985270	single nucleotide variant	NM_001168465.2(MAP7D2):c.1197A>C (p.Glu399Asp)	not specified [RCV005371405]	uncertain significance	X	20025763	20025763	Human		name
598197989	CV3985272	single nucleotide variant	NM_001168465.2(MAP7D2):c.2228C>G (p.Ser743Cys)	not specified [RCV005375492]	uncertain significance	X	20010897	20010897	Human		name
598176405	CV3985273	single nucleotide variant	NM_001168465.2(MAP7D2):c.2044A>G (p.Thr682Ala)	not specified [RCV005371407]	uncertain significance	X	20012377	20012377	Human		name
598176408	CV3985274	single nucleotide variant	NM_001168465.2(MAP7D2):c.2200A>G (p.Thr734Ala)	not specified [RCV005371408]	uncertain significance	X	20010925	20010925	Human		name
598176413	CV3985275	single nucleotide variant	NM_001168465.2(MAP7D2):c.1249G>A (p.Ala417Thr)	not specified [RCV005371409]	uncertain significance	X	20025711	20025711	Human		name
598176420	CV3985279	single nucleotide variant	NM_001168465.2(MAP7D2):c.1955A>G (p.Gln652Arg)	not specified [RCV005371410]	likely benign	X	20012466	20012466	Human		name
598198039	CV3985282	single nucleotide variant	NM_001168465.2(MAP7D2):c.1487A>T (p.Glu496Val)	not specified [RCV005375498]	uncertain significance	X	20016251	20016251	Human		name

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