Lrrc8b Variant Search Result - Rat Genome Database

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46 records found for search term Lrrc8b

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15140388	CV707562	single nucleotide variant	NM_001369817.2(LRRC8B):c.117C>T (p.Ala39=)	not provided [RCV000966129]	benign	1	89582767	89582767	Human		name
598222959	CV3984853	single nucleotide variant	NM_001369817.2(LRRC8B):c.70T>C (p.Trp24Arg)	not specified [RCV005379972]	uncertain significance	1	89582720	89582720	Human		name
15112358	CV707564	single nucleotide variant	NM_001369817.2(LRRC8B):c.879G>A (p.Val293=)	not provided [RCV000961286]	benign	1	89583529	89583529	Human		name
15111589	CV719120	single nucleotide variant	NM_001369817.2(LRRC8B):c.573G>A (p.Ser191=)	not provided [RCV000894294]	benign	1	89583223	89583223	Human		name
8576158	CV110513	single nucleotide variant	NM_001134476.1(LRRC8B):c.1209T>C (p.Asn403=)	Lung cancer [RCV000091036]	uncertain significance	1	89583859	89583859	Human		name
156106883	CV2214067	single nucleotide variant	NM_001369817.2(LRRC8B):c.218T>C (p.Leu73Pro)	not specified [RCV004084113]	uncertain significance	1	89582868	89582868	Human		name
156067307	CV2381078	single nucleotide variant	NM_001369817.2(LRRC8B):c.118G>A (p.Val40Met)	not specified [RCV004225112]	uncertain significance	1	89582768	89582768	Human		name
401731336	CV2674339	single nucleotide variant	NM_001369817.2(LRRC8B):c.199G>A (p.Ala67Thr)	not specified [RCV004289213]	uncertain significance	1	89582849	89582849	Human		name
401864878	CV2757259	single nucleotide variant	NM_001369817.2(LRRC8B):c.245A>C (p.Asn82Thr)	not specified [RCV004338851]	uncertain significance	1	89582895	89582895	Human		name
405656483	CV3288063	single nucleotide variant	NM_001369817.2(LRRC8B):c.191A>G (p.Asn64Ser)	not specified [RCV004415851]	uncertain significance	1	89582841	89582841	Human		name
405656486	CV3288064	single nucleotide variant	NM_001369817.2(LRRC8B):c.275G>A (p.Arg92Gln)	not specified [RCV004415852]	uncertain significance	1	89582925	89582925	Human		name
15172578	CV732634	single nucleotide variant	NM_001369817.2(LRRC8B):c.1918T>C (p.Leu640=)	not provided [RCV000905694]	likely benign	1	89584568	89584568	Human		name
156400825	CV2217243	single nucleotide variant	NM_001369817.2(LRRC8B):c.865T>G (p.Cys289Gly)	not specified [RCV004087695]	uncertain significance	1	89583515	89583515	Human		name
156143424	CV2358575	single nucleotide variant	NM_001369817.2(LRRC8B):c.322G>A (p.Val108Ile)	not specified [RCV004207456]	uncertain significance	1	89582972	89582972	Human		name
156072113	CV2365364	single nucleotide variant	NM_001369817.2(LRRC8B):c.661C>T (p.Pro221Ser)	not specified [RCV004209448]	uncertain significance	1	89583311	89583311	Human		name
401772452	CV2712738	single nucleotide variant	NM_001369817.2(LRRC8B):c.551C>A (p.Ser184Tyr)	not specified [RCV004308042]	uncertain significance	1	89583201	89583201	Human		name
405656491	CV3288065	single nucleotide variant	NM_001369817.2(LRRC8B):c.547C>T (p.Leu183Phe)	not specified [RCV004415853]	uncertain significance	1	89583197	89583197	Human		name
405656493	CV3288066	single nucleotide variant	NM_001369817.2(LRRC8B):c.728G>A (p.Arg243Lys)	not specified [RCV004415854]	uncertain significance	1	89583378	89583378	Human		name
597633609	CV3693633	single nucleotide variant	NM_001369817.2(LRRC8B):c.917A>G (p.Tyr306Cys)	not specified [RCV004940260]	uncertain significance	1	89583567	89583567	Human		name
597633630	CV3693636	single nucleotide variant	NM_001369817.2(LRRC8B):c.607A>C (p.Lys203Gln)	not specified [RCV004940263]	uncertain significance	1	89583257	89583257	Human		name
598251354	CV3984852	single nucleotide variant	NM_001369817.2(LRRC8B):c.617T>C (p.Leu206Ser)	not specified [RCV005366672]	uncertain significance	1	89583267	89583267	Human		name
15126563	CV707563	single nucleotide variant	NM_001369817.2(LRRC8B):c.862G>A (p.Asp288Asn)	not provided [RCV000963761]	benign	1	89583512	89583512	Human		name
155981163	CV2233048	single nucleotide variant	NM_001369817.2(LRRC8B):c.1726G>A (p.Val576Ile)	not specified [RCV004103684]	uncertain significance	1	89584376	89584376	Human		name
156257721	CV2322088	single nucleotide variant	NM_001369817.2(LRRC8B):c.1396A>C (p.Lys466Gln)	not specified [RCV004173831]	uncertain significance	1	89584046	89584046	Human		name
156395876	CV2325976	single nucleotide variant	NM_001369817.2(LRRC8B):c.2335A>C (p.Ile779Leu)	not specified [RCV004176189]	uncertain significance	1	89592966	89592966	Human		name
155984402	CV2344770	single nucleotide variant	NM_001369817.2(LRRC8B):c.1289A>G (p.Asn430Ser)	not specified [RCV004190923]	likely benign	1	89583939	89583939	Human		name
156165942	CV2398873	single nucleotide variant	NM_001369817.2(LRRC8B):c.1575G>C (p.Gln525His)	not specified [RCV004245194]	uncertain significance	1	89584225	89584225	Human		name
401725329	CV2697364	single nucleotide variant	NM_001369817.2(LRRC8B):c.1373C>T (p.Ala458Val)	not specified [RCV004304115]	uncertain significance	1	89584023	89584023	Human		name
401859855	CV2768369	single nucleotide variant	NM_001369817.2(LRRC8B):c.2383C>T (p.Arg795Cys)	not specified [RCV004350624]	uncertain significance	1	89593014	89593014	Human		name
405656458	CV3288056	single nucleotide variant	NM_001369817.2(LRRC8B):c.1291G>A (p.Gly431Ser)	not specified [RCV004415844]	uncertain significance	1	89583941	89583941	Human		name
405656461	CV3288057	single nucleotide variant	NM_001369817.2(LRRC8B):c.1469A>G (p.Lys490Arg)	not specified [RCV004415845]	uncertain significance	1	89584119	89584119	Human		name
405656464	CV3288058	single nucleotide variant	NM_001369817.2(LRRC8B):c.1573C>G (p.Gln525Glu)	not specified [RCV004415846]	uncertain significance	1	89584223	89584223	Human		name
405656472	CV3288060	single nucleotide variant	NM_001369817.2(LRRC8B):c.1587G>A (p.Met529Ile)	not specified [RCV004415848]	uncertain significance	1	89584237	89584237	Human		name
405656476	CV3288061	single nucleotide variant	NM_001369817.2(LRRC8B):c.1633T>G (p.Leu545Val)	not specified [RCV004415849]	uncertain significance	1	89584283	89584283	Human		name
405656479	CV3288062	single nucleotide variant	NM_001369817.2(LRRC8B):c.1840G>A (p.Asp614Asn)	not specified [RCV004415850]	uncertain significance	1	89584490	89584490	Human		name
407468249	CV3456636	single nucleotide variant	NM_001369817.2(LRRC8B):c.1115T>A (p.Leu372Gln)	not specified [RCV004636207]	uncertain significance	1	89583765	89583765	Human		name
407501304	CV3456637	single nucleotide variant	NM_001369817.2(LRRC8B):c.1892A>G (p.His631Arg)	not specified [RCV004644838]	uncertain significance	1	89584542	89584542	Human		name
407501308	CV3456638	single nucleotide variant	NM_001369817.2(LRRC8B):c.1292G>A (p.Gly431Asp)	not specified [RCV004644839]	uncertain significance	1	89583942	89583942	Human		name
407501312	CV3456639	single nucleotide variant	NM_001369817.2(LRRC8B):c.2215A>G (p.Asn739Asp)	not specified [RCV004644840]	uncertain significance	1	89592846	89592846	Human		name
597633595	CV3693630	single nucleotide variant	NM_001369817.2(LRRC8B):c.1630T>C (p.Tyr544His)	not specified [RCV004940258]	uncertain significance	1	89584280	89584280	Human		name
597633602	CV3693632	single nucleotide variant	NM_001369817.2(LRRC8B):c.2293C>T (p.Pro765Ser)	not specified [RCV004940259]	uncertain significance	1	89592924	89592924	Human		name
597633616	CV3693634	single nucleotide variant	NM_001369817.2(LRRC8B):c.2143G>A (p.Glu715Lys)	not specified [RCV004940261]	uncertain significance	1	89592774	89592774	Human		name
597633624	CV3693635	single nucleotide variant	NM_001369817.2(LRRC8B):c.2384G>A (p.Arg795His)	not specified [RCV004940262]	uncertain significance	1	89593015	89593015	Human		name
598222951	CV3984851	single nucleotide variant	NM_001369817.2(LRRC8B):c.1682C>T (p.Pro561Leu)	not specified [RCV005379971]	uncertain significance	1	89584332	89584332	Human		name
598222964	CV3984854	single nucleotide variant	NM_001369817.2(LRRC8B):c.1243G>C (p.Val415Leu)	not specified [RCV005379973]	uncertain significance	1	89583893	89583893	Human		name
15170434	CV696904	single nucleotide variant	NM_001369817.2(LRRC8B):c.1406G>A (p.Arg469His)	not provided [RCV000949649]	benign	1	89584056	89584056	Human		name

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