Nsun7 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

78 records found for search term Nsun7

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

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

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message