Apbb2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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71 records found for search term Apbb2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15156915	CV777474	single nucleotide variant	NM_004307.2(APBB2):c.20-6C>T	not provided [RCV000946788]	benign	4	41014404	41014404	Human		name
8579804	CV114206	single nucleotide variant	NM_004307.1(APBB2):c.-416-16544A>G	Lung cancer [RCV000094729]	uncertain significance	4	41159686	41159686	Human		name
597658135	CV3559430	single nucleotide variant	NM_004307.2(APBB2):c.10G>A (p.Val4Ile)	not specified [RCV004834563]	uncertain significance	4	41033245	41033245	Human		name
155914902	CV2203860	single nucleotide variant	NM_004307.2(APBB2):c.76G>A (p.Val26Ile)	not specified [RCV004069919]	uncertain significance	4	41014342	41014342	Human		name
156263378	CV2282572	single nucleotide variant	NM_004307.2(APBB2):c.75C>G (p.Asp25Glu)	not specified [RCV004135140]	uncertain significance	4	41014343	41014343	Human		name
597658193	CV3559438	single nucleotide variant	NM_004307.2(APBB2):c.51T>A (p.Phe17Leu)	not specified [RCV004834571]	uncertain significance	4	41014367	41014367	Human		name
156114041	CV2225011	single nucleotide variant	NM_004307.2(APBB2):c.159A>G (p.Ile53Met)	not specified [RCV004094844]	uncertain significance	4	41014259	41014259	Human		name
156050704	CV2328899	single nucleotide variant	NM_004307.2(APBB2):c.272G>C (p.Gly91Ala)	not specified [RCV004180208]	uncertain significance	4	41014146	41014146	Human		name
329376263	CV2438066	single nucleotide variant	NM_004307.2(APBB2):c.182G>A (p.Ser61Asn)	not specified [RCV004256855]	uncertain significance	4	41014236	41014236	Human		name
401743770	CV2688024	single nucleotide variant	NM_004307.2(APBB2):c.235A>G (p.Met79Val)	not specified [RCV004305098]	uncertain significance	4	41014183	41014183	Human		name
401893491	CV2765334	single nucleotide variant	NM_004307.2(APBB2):c.245C>T (p.Ser82Leu)	not specified [RCV004339845]	uncertain significance	4	41014173	41014173	Human		name
405661674	CV3289578	single nucleotide variant	NM_004307.2(APBB2):c.137A>G (p.Asn46Ser)	not specified [RCV004417521]	uncertain significance	4	41014281	41014281	Human		name
405661693	CV3289584	single nucleotide variant	NM_004307.2(APBB2):c.212C>T (p.Ala71Val)	not specified [RCV004417527]	uncertain significance	4	41014206	41014206	Human		name
405661696	CV3289585	single nucleotide variant	NM_004307.2(APBB2):c.215T>C (p.Leu72Pro)	not specified [RCV004417528]	uncertain significance	4	41014203	41014203	Human		name
405661702	CV3289587	single nucleotide variant	NM_004307.2(APBB2):c.230C>T (p.Ala77Val)	not specified [RCV004417530]	uncertain significance	4	41014188	41014188	Human		name
597657772	CV3559377	single nucleotide variant	NM_004307.2(APBB2):c.166A>C (p.Thr56Pro)	not specified [RCV004834511]	uncertain significance	4	41014252	41014252	Human		name
597657841	CV3559387	single nucleotide variant	NM_004307.2(APBB2):c.131C>T (p.Ser44Phe)	not specified [RCV004834521]	uncertain significance	4	41014287	41014287	Human		name
156322355	CV2205012	single nucleotide variant	NM_004307.2(APBB2):c.548A>G (p.His183Arg)	not specified [RCV004077629]	uncertain significance	4	41013870	41013870	Human		name
156229127	CV2209306	single nucleotide variant	NM_004307.2(APBB2):c.791C>T (p.Thr264Met)	not specified [RCV004091700]	uncertain significance	4	41013627	41013627	Human		name
156152306	CV2245328	single nucleotide variant	NM_004307.2(APBB2):c.934C>G (p.Pro312Ala)	not specified [RCV004107080]	uncertain significance	4	40944975	40944975	Human		name
155994708	CV2249295	single nucleotide variant	NM_004307.2(APBB2):c.377C>T (p.Ala126Val)	not specified [RCV004118320]	uncertain significance	4	41014041	41014041	Human		name
156166211	CV2270401	single nucleotide variant	NM_004307.2(APBB2):c.991T>C (p.Ser331Pro)	not specified [RCV004137381]	uncertain significance	4	40944918	40944918	Human		name
156074022	CV2281411	single nucleotide variant	NM_004307.2(APBB2):c.645G>T (p.Gln215His)	not specified [RCV004153747]	uncertain significance	4	41013773	41013773	Human		name
156361823	CV2322871	single nucleotide variant	NM_004307.2(APBB2):c.988G>C (p.Gly330Arg)	not specified [RCV004185329]	uncertain significance	4	40944921	40944921	Human		name
156068838	CV2341076	single nucleotide variant	NM_004307.2(APBB2):c.836C>T (p.Ala279Val)	not specified [RCV004181557]	uncertain significance	4	40945073	40945073	Human		name
155974735	CV2342586	single nucleotide variant	NM_004307.2(APBB2):c.323G>A (p.Arg108His)	not specified [RCV004196679]	uncertain significance	4	41014095	41014095	Human		name
401859897	CV2768389	single nucleotide variant	NM_004307.2(APBB2):c.964G>A (p.Val322Ile)	not specified [RCV004350640]	uncertain significance	4	40944945	40944945	Human		name
401892099	CV2777229	single nucleotide variant	NM_004307.2(APBB2):c.640C>T (p.Pro214Ser)	not specified [RCV004354260]	uncertain significance	4	41013778	41013778	Human		name
401880534	CV2792881	single nucleotide variant	NM_004307.2(APBB2):c.415G>A (p.Glu139Lys)	not specified [RCV004365619]	uncertain significance	4	41014003	41014003	Human		name
401880537	CV2792882	single nucleotide variant	NM_004307.2(APBB2):c.904G>A (p.Asp302Asn)	not specified [RCV004365620]	uncertain significance	4	40945005	40945005	Human		name
405661705	CV3289588	single nucleotide variant	NM_004307.2(APBB2):c.437C>T (p.Ser146Leu)	not specified [RCV004417531]	uncertain significance	4	41013981	41013981	Human		name
405661709	CV3289589	single nucleotide variant	NM_004307.2(APBB2):c.575C>A (p.Pro192Gln)	not specified [RCV004417532]	uncertain significance	4	41013843	41013843	Human		name
407522335	CV3459148	single nucleotide variant	NM_004307.2(APBB2):c.424C>G (p.Pro142Ala)	not specified [RCV004652841]	uncertain significance	4	41013994	41013994	Human		name
597657181	CV3559287	single nucleotide variant	NM_004307.2(APBB2):c.937A>G (p.Thr313Ala)	not specified [RCV004834427]	uncertain significance	4	40944972	40944972	Human		name
597657590	CV3559327	single nucleotide variant	NM_004307.2(APBB2):c.739C>G (p.Leu247Val)	not specified [RCV004834461]	uncertain significance	4	41013679	41013679	Human		name
597658532	CV3559355	single nucleotide variant	NM_004307.2(APBB2):c.613G>A (p.Asp205Asn)	not specified [RCV004834489]	uncertain significance	4	41013805	41013805	Human		name
597658466	CV3559366	single nucleotide variant	NM_004307.2(APBB2):c.332C>T (p.Ala111Val)	not specified [RCV004834500]	uncertain significance	4	41014086	41014086	Human		name
597658575	CV3559395	single nucleotide variant	NM_004307.2(APBB2):c.440G>T (p.Ser147Ile)	not specified [RCV004834529]	uncertain significance	4	41013978	41013978	Human		name
597657975	CV3559406	single nucleotide variant	NM_004307.2(APBB2):c.602T>C (p.Ile201Thr)	not specified [RCV004834540]	uncertain significance	4	41013816	41013816	Human		name
597658057	CV3559417	single nucleotide variant	NM_004307.2(APBB2):c.790A>G (p.Thr264Ala)	not specified [RCV004834551]	uncertain significance	4	41013628	41013628	Human		name
598253948	CV3990511	single nucleotide variant	NM_004307.2(APBB2):c.590C>T (p.Ala197Val)	not specified [RCV005385428]	uncertain significance	4	41013828	41013828	Human		name
598253968	CV3990519	single nucleotide variant	NM_004307.2(APBB2):c.605G>C (p.Gly202Ala)	not specified [RCV005385431]	uncertain significance	4	41013813	41013813	Human		name
598231063	CV3990527	single nucleotide variant	NM_004307.2(APBB2):c.863A>T (p.Gln288Leu)	not specified [RCV005381299]	uncertain significance	4	40945046	40945046	Human		name
598230868	CV4004086	single nucleotide variant	NM_004307.2(APBB2):c.950A>G (p.Gln317Arg)	not specified [RCV005381266]	uncertain significance	4	40944959	40944959	Human		name
598230901	CV4004095	single nucleotide variant	NM_004307.2(APBB2):c.799C>G (p.Gln267Glu)	not specified [RCV005381272]	uncertain significance	4	41013619	41013619	Human		name
598253923	CV4004112	single nucleotide variant	NM_004307.2(APBB2):c.959G>A (p.Arg320Gln)	not specified [RCV005385423]	uncertain significance	4	40944950	40944950	Human		name
156397569	CV2197260	single nucleotide variant	NM_004307.2(APBB2):c.1306G>A (p.Ala436Thr)	not specified [RCV004079036]	uncertain significance	4	40893360	40893360	Human		name
156085215	CV2205648	single nucleotide variant	NM_004307.2(APBB2):c.1372A>C (p.Ile458Leu)	not specified [RCV004082557]	uncertain significance	4	40893294	40893294	Human		name
155980192	CV2211909	single nucleotide variant	NM_004307.2(APBB2):c.2177C>T (p.Pro726Leu)	not specified [RCV004087041]	uncertain significance	4	40816195	40816195	Human		name
156022352	CV2223154	single nucleotide variant	NM_004307.2(APBB2):c.1639T>C (p.Ser547Pro)	not specified [RCV004103999]	uncertain significance	4	40830468	40830468	Human		name
156383116	CV2223785	single nucleotide variant	NM_004307.2(APBB2):c.1699A>G (p.Arg567Gly)	not specified [RCV004093858]	uncertain significance	4	40827165	40827165	Human		name
156165641	CV2243505	single nucleotide variant	NM_004307.2(APBB2):c.1144T>A (p.Leu382Ile)	not specified [RCV004112464]	uncertain significance	4	40934663	40934663	Human		name
156276183	CV2255761	single nucleotide variant	NM_004307.2(APBB2):c.1297G>A (p.Glu433Lys)	not specified [RCV004120145]	uncertain significance	4	40893369	40893369	Human		name
156254625	CV2325652	single nucleotide variant	NM_004307.2(APBB2):c.2180C>T (p.Ala727Val)	not specified [RCV004180061]	uncertain significance	4	40816192	40816192	Human		name
401773246	CV2698146	single nucleotide variant	NM_004307.2(APBB2):c.2167C>G (p.Pro723Ala)	not specified [RCV004302929]	uncertain significance	4	40816205	40816205	Human		name
401746459	CV2731806	single nucleotide variant	NM_004307.2(APBB2):c.2231C>T (p.Ser744Phe)	not specified [RCV004333059]	uncertain significance	4	40816141	40816141	Human		name
401897739	CV2772887	single nucleotide variant	NM_004307.2(APBB2):c.1499G>A (p.Arg500His)	not specified [RCV004357662]	uncertain significance	4	40890394	40890394	Human		name
405661671	CV3289577	single nucleotide variant	NM_004307.2(APBB2):c.1312G>A (p.Gly438Ser)	not specified [RCV004417520]	uncertain significance	4	40893354	40893354	Human		name
405661678	CV3289579	single nucleotide variant	NM_004307.2(APBB2):c.1489G>A (p.Val497Ile)	not specified [RCV004417522]	uncertain significance	4	40890404	40890404	Human		name
405661681	CV3289580	single nucleotide variant	NM_004307.2(APBB2):c.1714C>G (p.Leu572Val)	not specified [RCV004417523]	uncertain significance	4	40827150	40827150	Human		name
405661684	CV3289581	single nucleotide variant	NM_004307.2(APBB2):c.1777G>A (p.Val593Met)	not specified [RCV004417524]	uncertain significance	4	40825926	40825926	Human		name
405661687	CV3289582	single nucleotide variant	NM_004307.2(APBB2):c.1927G>A (p.Glu643Lys)	not specified [RCV004417525]	uncertain significance	4	40823649	40823649	Human		name
405661691	CV3289583	single nucleotide variant	NM_004307.2(APBB2):c.2090A>T (p.Glu697Val)	not specified [RCV004417526]	uncertain significance	4	40821893	40821893	Human		name
405661699	CV3289586	single nucleotide variant	NM_004307.2(APBB2):c.2173C>T (p.Pro725Ser)	not specified [RCV004417529]	uncertain significance	4	40816199	40816199	Human		name
407522364	CV3459159	single nucleotide variant	NM_004307.2(APBB2):c.1862C>T (p.Ser621Phe)	not specified [RCV004652849]	uncertain significance	4	40823714	40823714	Human		name
597657203	CV3559295	single nucleotide variant	NM_004307.2(APBB2):c.1793T>C (p.Met598Thr)	not specified [RCV004834430]	uncertain significance	4	40825910	40825910	Human		name
597657442	CV3559305	single nucleotide variant	NM_004307.2(APBB2):c.2006C>T (p.Thr669Ile)	not specified [RCV004834440]	uncertain significance	4	40821977	40821977	Human		name
597657518	CV3559316	single nucleotide variant	NM_004307.2(APBB2):c.1630G>A (p.Glu544Lys)	not specified [RCV004834451]	uncertain significance	4	40830477	40830477	Human		name
597657656	CV3559336	single nucleotide variant	NM_004307.2(APBB2):c.1510G>A (p.Val504Met)	not specified [RCV004834470]	uncertain significance	4	40890383	40890383	Human		name
597657723	CV3559346	single nucleotide variant	NM_004307.2(APBB2):c.1306G>C (p.Ala436Pro)	not specified [RCV004834480]	uncertain significance	4	40893360	40893360	Human		name
598230961	CV4004106	single nucleotide variant	NM_004307.2(APBB2):c.2261C>T (p.Pro754Leu)	not specified [RCV005381280]	uncertain significance	4	40816111	40816111	Human		name

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