Nsun7 Variant Search Result - Rat Genome Database

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78 records found for search term Nsun7

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401923285	CV2822502	single nucleotide variant	NM_024677.6(NSUN7):c.1037-5C>T	not provided [RCV003435009]	likely benign	4	40790597	40790597	Human		name
156013853	CV2300484	single nucleotide variant	NM_024677.6(NSUN7):c.5T>C (p.Leu2Pro)	not specified [RCV004153670]	uncertain significance	4	40750698	40750698	Human		name
405711147	CV3359523	single nucleotide variant	NM_024677.6(NSUN7):c.25G>A (p.Glu9Lys)	not specified [RCV004493871]	uncertain significance	4	40750718	40750718	Human		name
597708019	CV3577128	single nucleotide variant	NM_024677.6(NSUN7):c.10T>A (p.Ser4Thr)	not specified [RCV004840515]	uncertain significance	4	40750703	40750703	Human		name
597708025	CV3577129	single nucleotide variant	NM_024677.6(NSUN7):c.11C>T (p.Ser4Phe)	not specified [RCV004840516]	uncertain significance	4	40750704	40750704	Human		name
156032863	CV2275057	single nucleotide variant	NM_024677.6(NSUN7):c.59C>T (p.Ser20Phe)	not specified [RCV004136877]	uncertain significance	4	40750752	40750752	Human		name
329360981	CV2463166	single nucleotide variant	NM_024677.6(NSUN7):c.47C>T (p.Pro16Leu)	not specified [RCV004274949]	uncertain significance	4	40750740	40750740	Human		name
155905654	CV2303156	single nucleotide variant	NM_024677.6(NSUN7):c.238G>A (p.Glu80Lys)	not specified [RCV004156922]	uncertain significance	4	40750931	40750931	Human		name
155922937	CV2347410	single nucleotide variant	NM_024677.6(NSUN7):c.166G>A (p.Gly56Ser)	not specified [RCV004207248]	uncertain significance	4	40750859	40750859	Human		name
401721431	CV2673713	single nucleotide variant	NM_024677.6(NSUN7):c.125A>G (p.Tyr42Cys)	not specified [RCV004282441]	uncertain significance	4	40750818	40750818	Human		name
597707957	CV3577122	single nucleotide variant	NM_024677.6(NSUN7):c.220C>T (p.Pro74Ser)	not specified [RCV004840509]	uncertain significance	4	40750913	40750913	Human		name
598221216	CV3994812	single nucleotide variant	NM_024677.6(NSUN7):c.177C>G (p.Ile59Met)	not specified [RCV005379620]	uncertain significance	4	40750870	40750870	Human		name
598221223	CV3994813	single nucleotide variant	NM_024677.6(NSUN7):c.131A>G (p.Asp44Gly)	not specified [RCV005379621]	uncertain significance	4	40750824	40750824	Human		name
156141990	CV2199983	single nucleotide variant	NM_024677.6(NSUN7):c.955T>G (p.Ser319Ala)	not specified [RCV004074148]	uncertain significance	4	40776178	40776178	Human		name
156074608	CV2281455	single nucleotide variant	NM_024677.6(NSUN7):c.622A>G (p.Ile208Val)	not specified [RCV004153782]	uncertain significance	4	40774398	40774398	Human		name
156038379	CV2313636	single nucleotide variant	NM_024677.6(NSUN7):c.876G>T (p.Met292Ile)	not specified [RCV004157568]	uncertain significance	4	40776099	40776099	Human		name
155994526	CV2379554	single nucleotide variant	NM_024677.6(NSUN7):c.679T>C (p.Tyr227His)	not specified [RCV004217260]	uncertain significance	4	40774804	40774804	Human		name
155905249	CV2385737	single nucleotide variant	NM_024677.6(NSUN7):c.748G>A (p.Val250Ile)	not specified [RCV004226487]	uncertain significance	4	40774873	40774873	Human		name
329392785	CV2439182	single nucleotide variant	NM_024677.6(NSUN7):c.452T>A (p.Ile151Lys)	not specified [RCV004266458]	uncertain significance	4	40761265	40761265	Human		name
329374257	CV2443801	single nucleotide variant	NM_024677.6(NSUN7):c.425G>A (p.Arg142His)	not specified [RCV004258142]	uncertain significance	4	40761238	40761238	Human		name
329393150	CV2449524	single nucleotide variant	NM_024677.6(NSUN7):c.718G>A (p.Val240Ile)	not specified [RCV004268460]	uncertain significance	4	40774843	40774843	Human		name
401874109	CV2757832	single nucleotide variant	NM_024677.6(NSUN7):c.774A>C (p.Lys258Asn)	not specified [RCV004336979]	uncertain significance	4	40774899	40774899	Human		name
405711153	CV3359524	single nucleotide variant	NM_024677.6(NSUN7):c.331A>T (p.Ser111Cys)	not specified [RCV004493872]	uncertain significance	4	40760466	40760466	Human		name
405711166	CV3359526	single nucleotide variant	NM_024677.6(NSUN7):c.527G>A (p.Arg176Gln)	not specified [RCV004493874]	uncertain significance	4	40774303	40774303	Human		name
405711177	CV3359527	single nucleotide variant	NM_024677.6(NSUN7):c.616G>A (p.Ala206Thr)	not specified [RCV004493875]	uncertain significance	4	40774392	40774392	Human		name
405711183	CV3359528	single nucleotide variant	NM_024677.6(NSUN7):c.856G>A (p.Val286Ile)	not specified [RCV004493876]	uncertain significance	4	40776079	40776079	Human		name
405711190	CV3359529	single nucleotide variant	NM_024677.6(NSUN7):c.863C>T (p.Ala288Val)	not specified [RCV004493877]	uncertain significance	4	40776086	40776086	Human		name
405711196	CV3359530	single nucleotide variant	NM_024677.6(NSUN7):c.994G>T (p.Asp332Tyr)	not specified [RCV004493878]	uncertain significance	4	40776217	40776217	Human		name
407517350	CV3462108	single nucleotide variant	NM_024677.6(NSUN7):c.995A>T (p.Asp332Val)	not specified [RCV004650542]	uncertain significance	4	40776218	40776218	Human		name
407517339	CV3462113	single nucleotide variant	NM_024677.6(NSUN7):c.308T>C (p.Ile103Thr)	not specified [RCV004650546]	uncertain significance	4	40760443	40760443	Human		name
597707936	CV3577120	single nucleotide variant	NM_024677.6(NSUN7):c.536A>G (p.His179Arg)	not specified [RCV004840507]	uncertain significance	4	40774312	40774312	Human		name
597707967	CV3577123	single nucleotide variant	NM_024677.6(NSUN7):c.313G>A (p.Glu105Lys)	not specified [RCV004840510]	uncertain significance	4	40760448	40760448	Human		name
597708001	CV3577126	single nucleotide variant	NM_024677.6(NSUN7):c.934A>G (p.Ile312Val)	not specified [RCV004840513]	likely benign	4	40776157	40776157	Human		name
598265074	CV3994806	single nucleotide variant	NM_024677.6(NSUN7):c.632G>A (p.Cys211Tyr)	not specified [RCV005387880]	uncertain significance	4	40774408	40774408	Human		name
598221198	CV3994809	single nucleotide variant	NM_024677.6(NSUN7):c.424C>T (p.Arg142Cys)	not specified [RCV005379618]	uncertain significance	4	40761237	40761237	Human		name
598265084	CV3994814	single nucleotide variant	NM_024677.6(NSUN7):c.988G>A (p.Ala330Thr)	not specified [RCV005387882]	uncertain significance	4	40776211	40776211	Human		name
598265089	CV3994815	single nucleotide variant	NM_024677.6(NSUN7):c.902C>G (p.Thr301Arg)	not specified [RCV005387883]	uncertain significance	4	40776125	40776125	Human		name
598221232	CV3994816	single nucleotide variant	NM_024677.6(NSUN7):c.408T>G (p.Asp136Glu)	not specified [RCV005379622]	uncertain significance	4	40761221	40761221	Human		name
598265095	CV3994817	single nucleotide variant	NM_024677.6(NSUN7):c.685A>G (p.Lys229Glu)	not specified [RCV005387884]	uncertain significance	4	40774810	40774810	Human		name
156398012	CV2194120	single nucleotide variant	NM_024677.6(NSUN7):c.1795G>A (p.Ala599Thr)	not specified [RCV004076875]	uncertain significance	4	40808577	40808577	Human		name
156400885	CV2217370	single nucleotide variant	NM_024677.6(NSUN7):c.1859A>G (p.Lys620Arg)	not specified [RCV004087803]	uncertain significance	4	40808641	40808641	Human		name
155906279	CV2283476	single nucleotide variant	NM_024677.6(NSUN7):c.1771C>G (p.Gln591Glu)	not specified [RCV004139693]	uncertain significance	4	40808553	40808553	Human		name
155906285	CV2283477	single nucleotide variant	NM_024677.6(NSUN7):c.1774A>G (p.Lys592Glu)	not specified [RCV004139694]	uncertain significance	4	40808556	40808556	Human		name
156192454	CV2289424	single nucleotide variant	NM_024677.6(NSUN7):c.1882C>T (p.Arg628Cys)	not specified [RCV004152378]	uncertain significance	4	40808664	40808664	Human		name
156086440	CV2289957	single nucleotide variant	NM_024677.6(NSUN7):c.2029T>G (p.Cys677Gly)	not specified [RCV004150607]	uncertain significance	4	40808811	40808811	Human		name
156015919	CV2299015	single nucleotide variant	NM_024677.6(NSUN7):c.1735A>C (p.Asn579His)	not specified [RCV004158536]	uncertain significance	4	40808517	40808517	Human		name
155910321	CV2303568	single nucleotide variant	NM_024677.6(NSUN7):c.2033G>A (p.Arg678His)	not specified [RCV004161659]	likely benign	4	40808815	40808815	Human		name
156170967	CV2354924	single nucleotide variant	NM_024677.6(NSUN7):c.1645A>G (p.Lys549Glu)	not specified [RCV004191419]	uncertain significance	4	40808427	40808427	Human		name
329357055	CV2431234	single nucleotide variant	NM_024677.6(NSUN7):c.1067A>G (p.Asn356Ser)	not specified [RCV004250572]	uncertain significance	4	40790632	40790632	Human		name
329374408	CV2443889	single nucleotide variant	NM_024677.6(NSUN7):c.1733C>G (p.Ala578Gly)	not specified [RCV004258224]	uncertain significance	4	40808515	40808515	Human		name
401777584	CV2704178	single nucleotide variant	NM_024677.6(NSUN7):c.1846C>A (p.Pro616Thr)	not specified [RCV004311188]	uncertain significance	4	40808628	40808628	Human		name
401741380	CV2713482	single nucleotide variant	NM_024677.6(NSUN7):c.1040T>C (p.Ile347Thr)	not specified [RCV004319087]	uncertain significance	4	40790605	40790605	Human		name
401770014	CV2718995	single nucleotide variant	NM_024677.6(NSUN7):c.1473G>A (p.Met491Ile)	not specified [RCV004322583]	uncertain significance	4	40807133	40807133	Human		name
401742001	CV2721876	single nucleotide variant	NM_024677.6(NSUN7):c.2136G>T (p.Arg712Ser)	not specified [RCV004326385]	uncertain significance	4	40808918	40808918	Human		name
401751682	CV2727102	single nucleotide variant	NM_024677.6(NSUN7):c.1394C>T (p.Pro465Leu)	not specified [RCV004325468]	uncertain significance	4	40798898	40798898	Human		name
401769423	CV2735025	single nucleotide variant	NM_024677.6(NSUN7):c.1912C>T (p.Arg638Trp)	not specified [RCV004333725]	uncertain significance	4	40808694	40808694	Human		name
405711107	CV3359517	single nucleotide variant	NM_024677.6(NSUN7):c.1547C>T (p.Ser516Phe)	not specified [RCV004493865]	uncertain significance	4	40808329	40808329	Human		name
405711115	CV3359518	single nucleotide variant	NM_024677.6(NSUN7):c.1621C>T (p.Arg541Trp)	not specified [RCV004493866]	uncertain significance	4	40808403	40808403	Human		name
405711126	CV3359520	single nucleotide variant	NM_024677.6(NSUN7):c.1883G>A (p.Arg628His)	not specified [RCV004493868]	uncertain significance	4	40808665	40808665	Human		name
405711132	CV3359521	single nucleotide variant	NM_024677.6(NSUN7):c.1888C>T (p.Arg630Trp)	not specified [RCV004493869]	uncertain significance	4	40808670	40808670	Human		name
405711140	CV3359522	single nucleotide variant	NM_024677.6(NSUN7):c.1891C>A (p.Gln631Lys)	not specified [RCV004493870]	uncertain significance	4	40808673	40808673	Human		name
407517356	CV3462106	single nucleotide variant	NM_024677.6(NSUN7):c.1860G>T (p.Lys620Asn)	not specified [RCV004650540]	uncertain significance	4	40808642	40808642	Human		name
407517353	CV3462107	single nucleotide variant	NM_024677.6(NSUN7):c.1402C>A (p.Leu468Ile)	not specified [RCV004650541]	uncertain significance	4	40807062	40807062	Human		name
407477082	CV3462109	single nucleotide variant	NM_024677.6(NSUN7):c.2123C>G (p.Ser708Cys)	not specified [RCV004638760]	uncertain significance	4	40808905	40808905	Human		name
407517347	CV3462110	single nucleotide variant	NM_024677.6(NSUN7):c.1904T>C (p.Leu635Ser)	not specified [RCV004650543]	uncertain significance	4	40808686	40808686	Human		name
407517342	CV3462112	single nucleotide variant	NM_024677.6(NSUN7):c.1199A>C (p.Asp400Ala)	not specified [RCV004650545]	uncertain significance	4	40794393	40794393	Human		name
597707926	CV3577119	single nucleotide variant	NM_024677.6(NSUN7):c.1855G>A (p.Val619Met)	not specified [RCV004840506]	likely benign	4	40808637	40808637	Human		name
597707977	CV3577124	single nucleotide variant	NM_024677.6(NSUN7):c.1929G>T (p.Met643Ile)	not specified [RCV004840511]	uncertain significance	4	40808711	40808711	Human		name
597707987	CV3577125	single nucleotide variant	NM_024677.6(NSUN7):c.1985G>A (p.Ser662Asn)	not specified [RCV004840512]	uncertain significance	4	40808767	40808767	Human		name
597708010	CV3577127	single nucleotide variant	NM_024677.6(NSUN7):c.1411C>G (p.Pro471Ala)	not specified [RCV004840514]	uncertain significance	4	40807071	40807071	Human		name
597643330	CV3577130	single nucleotide variant	NM_024677.6(NSUN7):c.1988C>A (p.Pro663His)	not specified [RCV004832590]	uncertain significance	4	40808770	40808770	Human		name
598221181	CV3994807	single nucleotide variant	NM_024677.6(NSUN7):c.1715G>A (p.Arg572Gln)	not specified [RCV005379616]	uncertain significance	4	40808497	40808497	Human		name
598221189	CV3994808	single nucleotide variant	NM_024677.6(NSUN7):c.1880C>T (p.Pro627Leu)	not specified [RCV005379617]	uncertain significance	4	40808662	40808662	Human		name
598265079	CV3994810	single nucleotide variant	NM_024677.6(NSUN7):c.2038G>A (p.Val680Ile)	not specified [RCV005387881]	uncertain significance	4	40808820	40808820	Human		name
598221206	CV3994811	single nucleotide variant	NM_024677.6(NSUN7):c.1499G>A (p.Cys500Tyr)	not specified [RCV005379619]	uncertain significance	4	40807159	40807159	Human		name
598265100	CV3994818	single nucleotide variant	NM_024677.6(NSUN7):c.1906A>G (p.Arg636Gly)	not specified [RCV005387885]	uncertain significance	4	40808688	40808688	Human		name
598221239	CV3994819	single nucleotide variant	NM_024677.6(NSUN7):c.1662A>C (p.Lys554Asn)	not specified [RCV005379623]	uncertain significance	4	40808444	40808444	Human		name
598221248	CV3994820	single nucleotide variant	NM_024677.6(NSUN7):c.1664G>A (p.Gly555Asp)	not specified [RCV005379624]	uncertain significance	4	40808446	40808446	Human		name

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