Dhrs4 Variant Search Result - Rat Genome Database

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93 records found for search term Dhrs4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15175140	CV714082	single nucleotide variant	NM_021004.4(DHRS4):c.34C>A (p.Arg12=)	not provided [RCV000972874]	benign	14	23953822	23953822	Human		name
598162030	CV3953058	single nucleotide variant	NM_021004.4(DHRS4):c.26T>C (p.Leu9Pro)	not specified [RCV005329093]	uncertain significance	14	23953814	23953814	Human		name
598162046	CV3953061	single nucleotide variant	NM_021004.4(DHRS4):c.25C>T (p.Leu9Phe)	not specified [RCV005329096]	uncertain significance	14	23953813	23953813	Human		name
156154875	CV2266106	single nucleotide variant	NM_021004.4(DHRS4):c.71T>G (p.Met24Arg)	not specified [RCV004128700]	uncertain significance	14	23953859	23953859	Human		name
156052341	CV2269418	single nucleotide variant	NM_021004.4(DHRS4):c.74C>T (p.Thr25Ile)	not specified [RCV004124541]	uncertain significance	14	23953862	23953862	Human		name
155944207	CV2271611	single nucleotide variant	NM_021004.4(DHRS4):c.41G>C (p.Trp14Ser)	not specified [RCV004128689]	uncertain significance	14	23953829	23953829	Human		name
329399292	CV2436573	single nucleotide variant	NM_021004.4(DHRS4):c.56T>G (p.Met19Arg)	not specified [RCV004253726]	uncertain significance	14	23953844	23953844	Human		name
401876156	CV2777680	single nucleotide variant	NM_021004.4(DHRS4):c.59C>T (p.Ala20Val)	not specified [RCV004343516]	uncertain significance	14	23953847	23953847	Human		name
405691651	CV3247050	single nucleotide variant	NM_021004.4(DHRS4):c.94A>G (p.Asn32Asp)	not specified [RCV004373429]	uncertain significance	14	23953882	23953882	Human		name
15160781	CV702830	single nucleotide variant	NM_021004.4(DHRS4):c.390T>C (p.Thr130=)	not provided [RCV000947553]	likely benign	14	23959985	23959985	Human		name
155920705	CV2210866	single nucleotide variant	NM_021004.4(DHRS4):c.285C>G (p.Asp95Glu)	not specified [RCV004085952]	uncertain significance	14	23955191	23955191	Human		name
156165814	CV2243527	single nucleotide variant	NM_021004.4(DHRS4):c.286C>G (p.Arg96Gly)	not specified [RCV004112480]	uncertain significance	14	23955192	23955192	Human		name
156252260	CV2369025	single nucleotide variant	NM_021004.4(DHRS4):c.259G>C (p.Val87Leu)	not specified [RCV004207963]	uncertain significance	14	23955165	23955165	Human		name
401761086	CV2689019	single nucleotide variant	NM_021004.4(DHRS4):c.149G>A (p.Arg50Gln)	not specified [RCV004305798]	uncertain significance	14	23955055	23955055	Human		name
401859930	CV2768403	single nucleotide variant	NM_021004.4(DHRS4):c.229C>G (p.Gln77Glu)	not specified [RCV004350649]	uncertain significance	14	23955135	23955135	Human		name
405691597	CV3247040	single nucleotide variant	NM_021004.4(DHRS4):c.197A>C (p.Gln66Pro)	not specified [RCV004373419]	uncertain significance	14	23955103	23955103	Human		name
405691601	CV3247041	single nucleotide variant	NM_021004.4(DHRS4):c.206T>A (p.Val69Glu)	not specified [RCV004373420]	uncertain significance	14	23955112	23955112	Human		name
597659202	CV3652214	single nucleotide variant	NM_021004.4(DHRS4):c.224C>T (p.Thr75Met)	not specified [RCV004911612]	uncertain significance	14	23955130	23955130	Human		name
597659214	CV3652216	single nucleotide variant	NM_021004.4(DHRS4):c.215C>T (p.Ala72Val)	not specified [RCV004911614]	uncertain significance	14	23955121	23955121	Human		name
597659234	CV3652220	single nucleotide variant	NM_021004.4(DHRS4):c.276G>C (p.Lys92Asn)	not specified [RCV004911617]	uncertain significance	14	23955182	23955182	Human		name
597659247	CV3652222	single nucleotide variant	NM_021004.4(DHRS4):c.201G>C (p.Gln67His)	not specified [RCV004911619]	uncertain significance	14	23955107	23955107	Human		name
598162025	CV3953057	single nucleotide variant	NM_021004.4(DHRS4):c.292C>T (p.Arg98Trp)	not specified [RCV005329092]	uncertain significance	14	23955198	23955198	Human		name
598162036	CV3953059	single nucleotide variant	NM_021004.4(DHRS4):c.137T>C (p.Phe46Ser)	not specified [RCV005329094]	uncertain significance	14	23955043	23955043	Human		name
598162040	CV3953060	single nucleotide variant	NM_021004.4(DHRS4):c.217G>T (p.Val73Leu)	not specified [RCV005329095]	uncertain significance	14	23955123	23955123	Human		name
598162051	CV3953062	single nucleotide variant	NM_021004.4(DHRS4):c.152G>A (p.Arg51His)	not specified [RCV005329097]	uncertain significance	14	23955058	23955058	Human		name
598162062	CV3953064	single nucleotide variant	NM_021004.4(DHRS4):c.181G>A (p.Val61Ile)	not specified [RCV005329099]	likely benign	14	23955087	23955087	Human		name
15199533	CV753997	single nucleotide variant	NM_021004.4(DHRS4):c.191G>A (p.Arg64Gln)	not provided [RCV000912577]	likely benign	14	23955097	23955097	Human		name
156088974	CV2202026	single nucleotide variant	NM_021004.4(DHRS4):c.371G>A (p.Gly124Glu)	not specified [RCV004075947]	uncertain significance	14	23959966	23959966	Human		name
155920988	CV2212059	single nucleotide variant	NM_021004.4(DHRS4):c.775G>C (p.Asp259His)	not specified [RCV004088969]	uncertain significance	14	23968809	23968809	Human		name
156183959	CV2255396	single nucleotide variant	NM_021004.4(DHRS4):c.415G>A (p.Asp139Asn)	not specified [RCV004117761]	uncertain significance	14	23965768	23965768	Human		name
156287988	CV2301294	single nucleotide variant	NM_021004.4(DHRS4):c.730G>A (p.Glu244Lys)	not specified [RCV004160467]	likely benign	14	23968764	23968764	Human		name
156383883	CV2361722	single nucleotide variant	NM_021004.4(DHRS4):c.383A>C (p.Asp128Ala)	not specified [RCV004223201]	uncertain significance	14	23959978	23959978	Human		name
156257515	CV2368939	single nucleotide variant	NM_021004.4(DHRS4):c.805G>A (p.Val269Met)	not specified [RCV004207891]	uncertain significance	14	23968839	23968839	Human		name
329356740	CV2430883	single nucleotide variant	NM_021004.4(DHRS4):c.777T>A (p.Asp259Glu)	not specified [RCV004248082]	uncertain significance	14	23968811	23968811	Human		name
329358568	CV2454328	single nucleotide variant	NM_021004.4(DHRS4):c.541C>G (p.Pro181Ala)	not specified [RCV004265782]	uncertain significance	14	23966292	23966292	Human		name
401782086	CV2686523	single nucleotide variant	NM_021004.4(DHRS4):c.361C>A (p.Pro121Thr)	not specified [RCV004299962]	uncertain significance	14	23959956	23959956	Human		name
405691606	CV3247042	single nucleotide variant	NM_021004.4(DHRS4):c.484G>A (p.Gly162Ser)	not specified [RCV004373421]	uncertain significance	14	23965936	23965936	Human		name
405691617	CV3247044	single nucleotide variant	NM_021004.4(DHRS4):c.514G>C (p.Ala172Pro)	not specified [RCV004373423]	uncertain significance	14	23965966	23965966	Human		name
405691624	CV3247045	single nucleotide variant	NM_021004.4(DHRS4):c.517T>C (p.Phe173Leu)	not specified [RCV004373424]	uncertain significance	14	23965969	23965969	Human		name
405691628	CV3247046	single nucleotide variant	NM_021004.4(DHRS4):c.608G>A (p.Arg203Lys)	not specified [RCV004373425]	likely benign	14	23966359	23966359	Human		name
405691633	CV3247047	single nucleotide variant	NM_021004.4(DHRS4):c.675G>C (p.Met225Ile)	not specified [RCV004373426]	uncertain significance	14	23967219	23967219	Human		name
405691640	CV3247048	single nucleotide variant	NM_021004.4(DHRS4):c.778G>C (p.Ala260Pro)	not specified [RCV004373427]	uncertain significance	14	23968812	23968812	Human		name
405691646	CV3247049	single nucleotide variant	NM_021004.4(DHRS4):c.800C>T (p.Thr267Ile)	not specified [RCV004373428]	uncertain significance	14	23968834	23968834	Human		name
407467122	CV3434073	single nucleotide variant	NM_021004.4(DHRS4):c.481G>A (p.Gly161Ser)	not specified [RCV004614134]	uncertain significance	14	23965933	23965933	Human		name
407467126	CV3434074	single nucleotide variant	NM_021004.4(DHRS4):c.638G>A (p.Gly213Glu)	not specified [RCV004614135]	uncertain significance	14	23966389	23966389	Human		name
597659209	CV3652215	single nucleotide variant	NM_021004.4(DHRS4):c.326G>T (p.Gly109Val)	not specified [RCV004911613]	uncertain significance	14	23959921	23959921	Human		name
597659221	CV3652217	single nucleotide variant	NM_021004.4(DHRS4):c.619G>A (p.Val207Met)	not specified [RCV004911615]	uncertain significance	14	23966370	23966370	Human		name
597659226	CV3652219	single nucleotide variant	NM_021004.4(DHRS4):c.712C>T (p.Arg238Trp)	not specified [RCV004911616]	uncertain significance	14	23967256	23967256	Human		name
597659241	CV3652221	single nucleotide variant	NM_021004.4(DHRS4):c.298G>C (p.Val100Leu)	not specified [RCV004911618]	uncertain significance	14	23955204	23955204	Human		name
598162056	CV3953063	single nucleotide variant	NM_021004.4(DHRS4):c.449A>C (p.Lys150Thr)	not specified [RCV005329098]	uncertain significance	14	23965802	23965802	Human		name
598162079	CV3953067	single nucleotide variant	NM_021004.4(DHRS4):c.325G>T (p.Gly109Cys)	not specified [RCV005329102]	uncertain significance	14	23959920	23959920	Human		name
15104689	CV702831	single nucleotide variant	NM_021004.4(DHRS4):c.604C>T (p.Pro202Ser)	not provided [RCV000959735]	benign	14	23966355	23966355	Human		name
8583499	CV118061	single nucleotide variant	NM_001277864.1(DHRS4L1):c.148-791G>A	Lung cancer [RCV000098581]	uncertain significance	14	24047886	24047886	Human		name
9831957	CV167163	deletion	NM_001277864.1(DHRS4L1):c.-23423_-119+7390del	Large for gestational age [RCV000161730]\|Small for gestational age [RCV000161729]	not provided	14	23984157	24014851	Human		name
156243000	CV2246304	single nucleotide variant	NM_198083.4(DHRS4L2):c.16C>G (p.Leu6Val)	not specified [RCV004107750]	uncertain significance	14	23988963	23988963	Human		name
156271337	CV2312381	single nucleotide variant	NM_198083.4(DHRS4L2):c.25C>T (p.Leu9Phe)	not specified [RCV004167077]	uncertain significance	14	23988972	23988972	Human		name
155988385	CV2355079	single nucleotide variant	NM_198083.4(DHRS4L2):c.40C>G (p.Arg14Gly)	not specified [RCV004198473]	uncertain significance	14	23988987	23988987	Human		name
156002732	CV2396627	single nucleotide variant	NM_198083.4(DHRS4L2):c.34T>C (p.Trp12Arg)	not specified [RCV004240449]	likely benign	14	23988981	23988981	Human		name
405691679	CV3247055	single nucleotide variant	NM_198083.4(DHRS4L2):c.40C>T (p.Arg14Trp)	not specified [RCV004373434]	likely benign	14	23988987	23988987	Human		name
405691702	CV3247059	single nucleotide variant	NM_198083.4(DHRS4L2):c.98A>T (p.Lys33Met)	not specified [RCV004373438]	uncertain significance	14	23989045	23989045	Human		name
15097849	CV702832	single nucleotide variant	NM_198083.4(DHRS4L2):c.534C>A (p.Gly178=)	not provided [RCV000958409]	benign	14	24001386	24001386	Human		name
156107944	CV2214291	single nucleotide variant	NM_198083.4(DHRS4L2):c.139G>A (p.Ala47Thr)	not specified [RCV004086282]	uncertain significance	14	23990192	23990192	Human		name
156383325	CV2223872	single nucleotide variant	NM_198083.4(DHRS4L2):c.287G>A (p.Arg96Gln)	not specified [RCV004093886]	uncertain significance	14	23990340	23990340	Human		name
156048682	CV2271744	single nucleotide variant	NM_198083.4(DHRS4L2):c.179T>C (p.Val60Ala)	not specified [RCV004130589]	uncertain significance	14	23990232	23990232	Human		name
155925065	CV2277236	single nucleotide variant	NM_198083.4(DHRS4L2):c.236A>T (p.Glu79Val)	not specified [RCV004142858]	uncertain significance	14	23990289	23990289	Human		name
155906792	CV2379132	single nucleotide variant	NM_198083.4(DHRS4L2):c.278C>T (p.Ala93Val)	not specified [RCV004235927]	uncertain significance	14	23990331	23990331	Human		name
329380931	CV2440486	single nucleotide variant	NM_198083.4(DHRS4L2):c.151C>A (p.Arg51Ser)	not specified [RCV004256412]	uncertain significance	14	23990204	23990204	Human		name
329390716	CV2455404	single nucleotide variant	NM_198083.4(DHRS4L2):c.133G>A (p.Gly45Ser)	not specified [RCV004274894]	uncertain significance	14	23990186	23990186	Human		name
401878620	CV2770723	single nucleotide variant	NM_198083.4(DHRS4L2):c.175G>A (p.Val59Met)	not specified [RCV004349767]	uncertain significance	14	23990228	23990228	Human		name
405691657	CV3247051	single nucleotide variant	NM_198083.4(DHRS4L2):c.292C>T (p.Arg98Trp)	not specified [RCV004373430]	uncertain significance	14	23990345	23990345	Human		name
597659252	CV3652223	single nucleotide variant	NM_198083.4(DHRS4L2):c.251C>T (p.Thr84Met)	not specified [RCV004911620]	uncertain significance	14	23990304	23990304	Human		name
597659256	CV3652224	single nucleotide variant	NM_198083.4(DHRS4L2):c.217G>A (p.Val73Met)	not specified [RCV004911621]	uncertain significance	14	23990270	23990270	Human		name
598162098	CV3953070	single nucleotide variant	NM_198083.4(DHRS4L2):c.160C>A (p.Gln54Lys)	not specified [RCV005329105]	uncertain significance	14	23990213	23990213	Human		name
598162103	CV3953071	single nucleotide variant	NM_198083.4(DHRS4L2):c.181G>A (p.Val61Ile)	not specified [RCV005329106]	likely benign	14	23990234	23990234	Human		name
156098853	CV2306497	single nucleotide variant	NM_198083.4(DHRS4L2):c.419T>C (p.Ile140Thr)	not specified [RCV004157114]	uncertain significance	14	24000873	24000873	Human		name
156098751	CV2370818	single nucleotide variant	NM_198083.4(DHRS4L2):c.331G>A (p.Asp111Asn)	not specified [RCV004209211]	uncertain significance	14	23995056	23995056	Human		name
155907181	CV2389796	single nucleotide variant	NM_198083.4(DHRS4L2):c.374G>A (p.Ser125Asn)	not specified [RCV004236023]	likely benign	14	23995099	23995099	Human		name
329387780	CV2446796	single nucleotide variant	NM_198083.4(DHRS4L2):c.481G>A (p.Gly161Ser)	not specified [RCV004257655]	uncertain significance	14	24001034	24001034	Human		name
329364665	CV2447552	single nucleotide variant	NM_198083.4(DHRS4L2):c.350C>T (p.Ala117Val)	not specified [RCV004255908]	uncertain significance	14	23995075	23995075	Human		name
329352931	CV2468037	single nucleotide variant	NM_198083.4(DHRS4L2):c.515C>A (p.Ala172Asp)	not specified [RCV004273654]	uncertain significance	14	24001068	24001068	Human		name
401895380	CV2786421	single nucleotide variant	NM_198083.4(DHRS4L2):c.326G>A (p.Gly109Asp)	not specified [RCV004362008]	uncertain significance	14	23995051	23995051	Human		name
405691662	CV3247052	single nucleotide variant	NM_198083.4(DHRS4L2):c.330C>G (p.Ile110Met)	not specified [RCV004373431]	uncertain significance	14	23995055	23995055	Human		name
405691669	CV3247053	single nucleotide variant	NM_198083.4(DHRS4L2):c.340G>C (p.Val114Leu)	not specified [RCV004373432]	uncertain significance	14	23995065	23995065	Human		name
405691675	CV3247054	single nucleotide variant	NM_198083.4(DHRS4L2):c.403G>A (p.Asp135Asn)	not specified [RCV004373433]	uncertain significance	14	23995128	23995128	Human		name
405692727	CV3247056	single nucleotide variant	NM_198083.4(DHRS4L2):c.592A>C (p.Ile198Leu)	not specified [RCV004373435]	uncertain significance	14	24001444	24001444	Human		name
405691689	CV3247057	single nucleotide variant	NM_198083.4(DHRS4L2):c.619G>A (p.Val207Met)	not specified [RCV004373436]	uncertain significance	14	24001471	24001471	Human		name
405691695	CV3247058	single nucleotide variant	NM_198083.4(DHRS4L2):c.633C>G (p.His211Gln)	not specified [RCV004373437]	uncertain significance	14	24001485	24001485	Human		name
407467131	CV3434075	single nucleotide variant	NM_198083.4(DHRS4L2):c.499G>A (p.Val167Met)	not specified [RCV004614136]	uncertain significance	14	24001052	24001052	Human		name
407467135	CV3434076	single nucleotide variant	NM_198083.4(DHRS4L2):c.348T>A (p.Asn116Lys)	not specified [RCV004614137]	uncertain significance	14	23995073	23995073	Human		name
597659262	CV3652225	single nucleotide variant	NM_198083.4(DHRS4L2):c.418A>G (p.Ile140Val)	not specified [RCV004911622]	uncertain significance	14	24000872	24000872	Human		name
597659267	CV3652226	single nucleotide variant	NM_198083.4(DHRS4L2):c.367T>A (p.Phe123Ile)	not specified [RCV004911623]	uncertain significance	14	23995092	23995092	Human		name
598162085	CV3953068	single nucleotide variant	NM_198083.4(DHRS4L2):c.642A>C (p.Leu214Phe)	not specified [RCV005329103]	uncertain significance	14	24001494	24001494	Human		name
598162091	CV3953069	single nucleotide variant	NM_198083.4(DHRS4L2):c.519C>A (p.Phe173Leu)	not specified [RCV005329104]	uncertain significance	14	24001072	24001072	Human		name

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