Ankrd33b Variant Search Result - Rat Genome Database

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67 records found for search term Ankrd33b

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8580221	CV114648	single nucleotide variant	NM_001164440.1(ANKRD33B):c.638-781C>T	Lung cancer [RCV000095171]	uncertain significance	5	10648485	10648485	Human		name
8580218	CV114645	single nucleotide variant	NM_001164440.1(ANKRD33B):c.496+6070C>T	Lung cancer [RCV000095168]	uncertain significance	5	10624532	10624532	Human		name
405660508	CV3278639	single nucleotide variant	NM_001164440.2(ANKRD33B):c.53C>T (p.Thr18Ile)	not specified [RCV004417125]	uncertain significance	5	10564520	10564520	Human		name
405660539	CV3278651	single nucleotide variant	NM_001164440.2(ANKRD33B):c.74C>G (p.Pro25Arg)	not specified [RCV004417137]	uncertain significance	5	10564541	10564541	Human		name
156181957	CV2298573	single nucleotide variant	NM_001164440.2(ANKRD33B):c.248T>G (p.Val83Gly)	not specified [RCV004162223]	uncertain significance	5	10564715	10564715	Human		name
401880976	CV2763199	single nucleotide variant	NM_001164440.2(ANKRD33B):c.211A>G (p.Ser71Gly)	not specified [RCV004336236]	uncertain significance	5	10564678	10564678	Human		name
405660396	CV3278599	single nucleotide variant	NM_001164440.2(ANKRD33B):c.131C>G (p.Ser44Trp)	not specified [RCV004417085]	uncertain significance	5	10564598	10564598	Human		name
407515021	CV3454420	single nucleotide variant	NM_001164440.2(ANKRD33B):c.109T>C (p.Tyr37His)	not specified [RCV004649731]	uncertain significance	5	10564576	10564576	Human		name
407504329	CV3454435	single nucleotide variant	NM_001164440.2(ANKRD33B):c.112G>A (p.Glu38Lys)	not specified [RCV004645770]	uncertain significance	5	10564579	10564579	Human		name
407515051	CV3454439	single nucleotide variant	NM_001164440.2(ANKRD33B):c.181T>G (p.Phe61Val)	not specified [RCV004649742]	uncertain significance	5	10564648	10564648	Human		name
597635259	CV3557652	single nucleotide variant	NM_001164440.2(ANKRD33B):c.290A>G (p.Asn97Ser)	not specified [RCV004831152]	uncertain significance	5	10564757	10564757	Human		name
597635270	CV3557655	single nucleotide variant	NM_001164440.2(ANKRD33B):c.245G>C (p.Ser82Thr)	not specified [RCV004831154]	uncertain significance	5	10564712	10564712	Human		name
156315010	CV2196730	single nucleotide variant	NM_001164440.2(ANKRD33B):c.355C>A (p.Arg119Ser)	not specified [RCV004069414]	uncertain significance	5	10564822	10564822	Human		name
156399828	CV2202249	single nucleotide variant	NM_001164440.2(ANKRD33B):c.878C>T (p.Pro293Leu)	not specified [RCV004078192]	uncertain significance	5	10649506	10649506	Human		name
156385841	CV2228049	single nucleotide variant	NM_001164440.2(ANKRD33B):c.901G>A (p.Asp301Asn)	not provided [RCV004695406]\|not specified [RCV004096288]	uncertain significance	5	10649529	10649529	Human		name
155974709	CV2235755	single nucleotide variant	NM_001164440.2(ANKRD33B):c.370G>A (p.Gly124Ser)	not specified [RCV004111888]	uncertain significance	5	10618336	10618336	Human		name
156207540	CV2250048	single nucleotide variant	NM_001164440.2(ANKRD33B):c.859G>C (p.Val287Leu)	not specified [RCV004116875]	likely benign	5	10649487	10649487	Human		name
156134798	CV2256774	single nucleotide variant	NM_001164440.2(ANKRD33B):c.859G>T (p.Val287Leu)	not specified [RCV004120999]	likely benign	5	10649487	10649487	Human		name
156303131	CV2258785	single nucleotide variant	NM_001164440.2(ANKRD33B):c.800C>T (p.Pro267Leu)	not specified [RCV004118014]	uncertain significance	5	10649428	10649428	Human		name
156182210	CV2288233	single nucleotide variant	NM_001164440.2(ANKRD33B):c.638G>T (p.Gly213Val)	not specified [RCV004149744]	uncertain significance	5	10649266	10649266	Human		name
156153289	CV2307703	single nucleotide variant	NM_001164440.2(ANKRD33B):c.356G>C (p.Arg119Pro)	not specified [RCV004168112]	uncertain significance	5	10564823	10564823	Human		name
156161429	CV2319469	single nucleotide variant	NM_001164440.2(ANKRD33B):c.971G>C (p.Cys324Ser)	not specified [RCV004185048]	uncertain significance	5	10649599	10649599	Human		name
155921379	CV2340441	single nucleotide variant	NM_001164440.2(ANKRD33B):c.428G>A (p.Cys143Tyr)	not specified [RCV004197168]	uncertain significance	5	10618394	10618394	Human		name
155930115	CV2366558	single nucleotide variant	NM_001164440.2(ANKRD33B):c.745C>T (p.Arg249Cys)	not specified [RCV004208531]	uncertain significance	5	10649373	10649373	Human		name
155960002	CV2390619	single nucleotide variant	NM_001164440.2(ANKRD33B):c.409G>C (p.Val137Leu)	not specified [RCV004239142]	uncertain significance	5	10618375	10618375	Human		name
155927241	CV2396065	single nucleotide variant	NM_001164440.2(ANKRD33B):c.998C>T (p.Pro333Leu)	not specified [RCV004237601]	uncertain significance	5	10649626	10649626	Human		name
329400873	CV2445838	single nucleotide variant	NM_001164440.2(ANKRD33B):c.731A>G (p.Gln244Arg)	not specified [RCV004270458]	uncertain significance	5	10649359	10649359	Human		name
329387187	CV2463420	single nucleotide variant	NM_001164440.2(ANKRD33B):c.993C>A (p.Ser331Arg)	not specified [RCV004277255]	uncertain significance	5	10649621	10649621	Human		name
401727036	CV2684442	single nucleotide variant	NM_001164440.2(ANKRD33B):c.511A>G (p.Thr171Ala)	not specified [RCV004291516]	uncertain significance	5	10638042	10638042	Human		name
401761166	CV2726664	single nucleotide variant	NM_001164440.2(ANKRD33B):c.820G>A (p.Ala274Thr)	not specified [RCV004323007]	uncertain significance	5	10649448	10649448	Human		name
405660494	CV3278634	single nucleotide variant	NM_001164440.2(ANKRD33B):c.448T>G (p.Trp150Gly)	not specified [RCV004417120]	uncertain significance	5	10618414	10618414	Human		name
405660523	CV3278645	single nucleotide variant	NM_001164440.2(ANKRD33B):c.736C>A (p.Leu246Met)	not specified [RCV004417131]	uncertain significance	5	10649364	10649364	Human		name
405660576	CV3278663	single nucleotide variant	NM_001164440.2(ANKRD33B):c.857G>T (p.Cys286Phe)	not specified [RCV004417149]	likely benign	5	10649485	10649485	Human		name
405660609	CV3278675	single nucleotide variant	NM_001164440.2(ANKRD33B):c.991A>G (p.Ser331Gly)	not specified [RCV004417161]	uncertain significance	5	10649619	10649619	Human		name
405660627	CV3278681	single nucleotide variant	NM_001164440.2(ANKRD33B):c.994C>T (p.Pro332Ser)	not specified [RCV004417167]	uncertain significance	5	10649622	10649622	Human		name
407515044	CV3454429	single nucleotide variant	NM_001164440.2(ANKRD33B):c.503C>T (p.Ala168Val)	not specified [RCV004649739]	uncertain significance	5	10638034	10638034	Human		name
597635238	CV3557643	single nucleotide variant	NM_001164440.2(ANKRD33B):c.354C>G (p.Asp118Glu)	not specified [RCV004831148]	uncertain significance	5	10564821	10564821	Human		name
597635243	CV3557644	single nucleotide variant	NM_001164440.2(ANKRD33B):c.742G>A (p.Glu248Lys)	not specified [RCV004831149]	uncertain significance	5	10649370	10649370	Human		name
597638266	CV3557645	single nucleotide variant	NM_001164440.2(ANKRD33B):c.958G>T (p.Val320Leu)	not specified [RCV004824916]	uncertain significance	5	10649586	10649586	Human		name
597635248	CV3557647	single nucleotide variant	NM_001164440.2(ANKRD33B):c.727A>C (p.Met243Leu)	not specified [RCV004831150]	uncertain significance	5	10649355	10649355	Human		name
597638277	CV3557653	single nucleotide variant	NM_001164440.2(ANKRD33B):c.583A>G (p.Met195Val)	not specified [RCV004824918]	uncertain significance	5	10638114	10638114	Human		name
597638282	CV3557664	single nucleotide variant	NM_001164440.2(ANKRD33B):c.595A>G (p.Met199Val)	not specified [RCV004824919]	uncertain significance	5	10638126	10638126	Human		name
598254938	CV3993328	single nucleotide variant	NM_001164440.2(ANKRD33B):c.467A>C (p.Asn156Thr)	not specified [RCV005367272]	uncertain significance	5	10618433	10618433	Human		name
156136667	CV2210279	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1162C>T (p.Pro388Ser)	not specified [RCV004089443]	uncertain significance	5	10649790	10649790	Human		name
155976268	CV2231635	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1163C>T (p.Pro388Leu)	not specified [RCV004098207]	uncertain significance	5	10649791	10649791	Human		name
156271123	CV2237111	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1108C>T (p.Arg370Trp)	not specified [RCV004114866]	uncertain significance	5	10649736	10649736	Human		name
155945195	CV2291998	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1280G>T (p.Arg427Leu)	not specified [RCV004160286]	uncertain significance	5	10649908	10649908	Human		name
156053795	CV2308605	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1118A>G (p.Gln373Arg)	not specified [RCV004167164]	uncertain significance	5	10649746	10649746	Human		name
156326454	CV2331950	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1457G>A (p.Arg486His)	not specified [RCV004187011]	uncertain significance	5	10650085	10650085	Human		name
156072209	CV2335010	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1124A>G (p.Asp375Gly)	not specified [RCV004182101]	uncertain significance	5	10649752	10649752	Human		name
156189220	CV2375503	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1396G>A (p.Glu466Lys)	not specified [RCV004226014]	uncertain significance	5	10650024	10650024	Human		name
156103902	CV2400246	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1363A>C (p.Ile455Leu)	not specified [RCV004243038]	likely benign	5	10649991	10649991	Human		name
401772442	CV2687529	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1061C>T (p.Pro354Leu)	not specified [RCV004300759]	uncertain significance	5	10649689	10649689	Human		name
401736120	CV2689262	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1142G>A (p.Gly381Asp)	not specified [RCV004306103]	uncertain significance	5	10649770	10649770	Human		name
401769809	CV2689961	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1421A>C (p.Glu474Ala)	not specified [RCV004297846]	uncertain significance	5	10650049	10650049	Human		name
401754623	CV2722912	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1198G>T (p.Ala400Ser)	not specified [RCV004327096]	likely benign	5	10649826	10649826	Human		name
405660279	CV3278562	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1043C>T (p.Ala348Val)	not specified [RCV004417048]	uncertain significance	5	10649671	10649671	Human		name
405660291	CV3278565	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1069C>A (p.Gln357Lys)	not specified [RCV004417051]	uncertain significance	5	10649697	10649697	Human		name
405660368	CV3278590	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1280G>A (p.Arg427Gln)	not specified [RCV004417076]	uncertain significance	5	10649908	10649908	Human		name
405660408	CV3278603	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1350C>A (p.Ser450Arg)	not specified [RCV004417089]	uncertain significance	5	10649978	10649978	Human		name
407504332	CV3454436	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1045C>T (p.Arg349Trp)	not specified [RCV004645771]	uncertain significance	5	10649673	10649673	Human		name
597635254	CV3557650	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1478G>A (p.Arg493Lys)	not specified [RCV004831151]	uncertain significance	5	10650106	10650106	Human		name
597635264	CV3557654	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1351G>A (p.Gly451Ser)	not specified [RCV004831153]	uncertain significance	5	10649979	10649979	Human		name
597635274	CV3557657	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1024G>A (p.Val342Met)	not specified [RCV004831155]	uncertain significance	5	10649652	10649652	Human		name
598186793	CV3993299	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1187C>T (p.Pro396Leu)	not specified [RCV005373463]	uncertain significance	5	10649815	10649815	Human		name
598186853	CV3993319	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1295C>G (p.Pro432Arg)	not specified [RCV005373472]	uncertain significance	5	10649923	10649923	Human		name
598254960	CV3993336	single nucleotide variant	NM_001164440.2(ANKRD33B):c.1109G>A (p.Arg370Gln)	not specified [RCV005367275]	uncertain significance	5	10649737	10649737	Human		name

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