Lgals3 Variant Search Result - Rat Genome Database

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82 records found for search term Lgals3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15152709	CV730942	single nucleotide variant	NM_002306.4(LGALS3):c.18+7G>A	not provided [RCV000879862]	benign	14	55137398	55137398	Human		name
8583852	CV118417	single nucleotide variant	NM_002306.3(LGALS3):c.431+499G>A	Lung cancer [RCV000098937]	uncertain significance	14	55140862	55140862	Human		name
401902023	CV2810435	single nucleotide variant	NM_002306.4(LGALS3):c.18G>A (p.Ser6=)	not provided [RCV003393439]	likely benign	14	55137391	55137391	Human	1	name
401902023	CV2810435	single nucleotide variant	NM_002306.4(LGALS3):c.18G>A (p.Ser6=)	not provided [RCV003393439]	likely benign	14	55137391	55137392	Human	1	name
15151041	CV739244	single nucleotide variant	NM_002306.4(LGALS3):c.24T>C (p.His8=)	not provided [RCV000901280]	benign	14	55138050	55138050	Human		name
401902024	CV2810436	single nucleotide variant	NM_002306.4(LGALS3):c.72C>T (p.Gly24=)	not provided [RCV003393440]	likely benign	14	55138098	55138098	Human		name
15174974	CV725700	single nucleotide variant	NM_002306.4(LGALS3):c.30G>A (p.Ala10=)	not provided [RCV000884254]	likely benign	14	55138056	55138056	Human		name
15200068	CV702904	single nucleotide variant	NM_002306.4(LGALS3):c.294C>T (p.Thr98=)	not provided [RCV000957223]	benign	14	55138320	55138320	Human		name
156207919	CV2360489	single nucleotide variant	NM_002306.4(LGALS3):c.89C>G (p.Pro30Arg)	not specified [RCV004210854]	uncertain significance	14	55138115	55138115	Human		name
598236719	CV3984453	single nucleotide variant	NM_002306.4(LGALS3):c.76T>C (p.Trp26Arg)	not specified [RCV005363925]	uncertain significance	14	55138102	55138102	Human		name
15099123	CV769830	single nucleotide variant	NM_002306.4(LGALS3):c.498C>T (p.Asn166=)	not provided [RCV000936426]	likely benign	14	55142650	55142650	Human		name
597641305	CV3696098	single nucleotide variant	NM_002306.4(LGALS3):c.124C>T (p.Pro42Ser)	not specified [RCV004941670]	uncertain significance	14	55138150	55138150	Human		name
597641316	CV3696100	single nucleotide variant	NM_002306.4(LGALS3):c.131C>T (p.Ala44Val)	not specified [RCV004941672]	uncertain significance	14	55138157	55138157	Human		name
598236728	CV3984455	single nucleotide variant	NM_002306.4(LGALS3):c.109C>A (p.Pro37Thr)	not specified [RCV005363927]	uncertain significance	14	55138135	55138135	Human		name
155987120	CV2234065	single nucleotide variant	NM_002306.4(LGALS3):c.485G>A (p.Arg162His)	not specified [RCV004106171]	uncertain significance	14	55142637	55142637	Human		name
156080114	CV2300978	single nucleotide variant	NM_002306.4(LGALS3):c.545G>A (p.Gly182Glu)	not specified [RCV004158150]	uncertain significance	14	55142697	55142697	Human		name
156328760	CV2332309	single nucleotide variant	NM_002306.4(LGALS3):c.671G>A (p.Arg224Gln)	not specified [RCV004182479]	uncertain significance	14	55145189	55145189	Human		name
156011718	CV2358771	single nucleotide variant	NM_002306.4(LGALS3):c.386G>A (p.Arg129His)	not specified [RCV004210078]	uncertain significance	14	55140318	55140318	Human		name
156269629	CV2398594	single nucleotide variant	NM_002306.4(LGALS3):c.422A>G (p.Asn141Ser)	not specified [RCV004237905]	uncertain significance	14	55140354	55140354	Human		name
405817824	CV3280327	single nucleotide variant	NM_002306.4(LGALS3):c.320A>G (p.Tyr107Cys)	not specified [RCV004412834]	uncertain significance	14	55138346	55138346	Human		name
407492067	CV3452746	single nucleotide variant	NM_002306.4(LGALS3):c.576T>G (p.Phe192Leu)	not specified [RCV004642381]	uncertain significance	14	55142728	55142728	Human		name
597641300	CV3696097	single nucleotide variant	NM_002306.4(LGALS3):c.710C>T (p.Ser237Phe)	not specified [RCV004941669]	uncertain significance	14	55145228	55145228	Human		name
597641309	CV3696099	single nucleotide variant	NM_002306.4(LGALS3):c.368C>T (p.Pro123Leu)	not specified [RCV004941671]	uncertain significance	14	55140300	55140300	Human		name
15160866	CV702905	single nucleotide variant	NM_002306.4(LGALS3):c.548G>A (p.Arg183Lys)	not provided [RCV000947568]	benign	14	55142700	55142700	Human		name
405817833	CV3280336	single nucleotide variant	NM_005567.4(LGALS3BP):c.7C>T (p.Pro3Ser)	not specified [RCV004412843]	uncertain significance	17	78977185	78977185	Human		name
598236743	CV3984460	single nucleotide variant	NM_005567.4(LGALS3BP):c.4A>G (p.Thr2Ala)	not specified [RCV005363930]	likely benign	17	78977188	78977188	Human		name
407492076	CV3452749	single nucleotide variant	NM_005567.4(LGALS3BP):c.11C>T (p.Pro4Leu)	not specified [RCV004642383]	likely benign	17	78977181	78977181	Human		name
15150499	CV741093	single nucleotide variant	NM_005567.4(LGALS3BP):c.282G>A (p.Thr94=)	not provided [RCV000901167]	benign	17	78974782	78974782	Human		name
156165834	CV2243528	single nucleotide variant	NM_005567.4(LGALS3BP):c.92C>T (p.Ala31Val)	not specified [RCV004112481]	uncertain significance	17	78976117	78976117	Human		name
156297201	CV2297654	single nucleotide variant	NM_005567.4(LGALS3BP):c.91G>T (p.Ala31Ser)	not specified [RCV004155341]	uncertain significance	17	78976118	78976118	Human		name
597641340	CV3696104	single nucleotide variant	NM_005567.4(LGALS3BP):c.61G>C (p.Asp21His)	not specified [RCV004941676]	uncertain significance	17	78976148	78976148	Human		name
15167837	CV727486	single nucleotide variant	NM_005567.4(LGALS3BP):c.999T>C (p.Arg333=)	not provided [RCV000882930]	benign	17	78972335	78972335	Human		name
15099953	CV756190	single nucleotide variant	NM_005567.4(LGALS3BP):c.420G>T (p.Ser140=)	not provided [RCV000914534]	likely benign	17	78973179	78973179	Human		name
405817829	CV3280332	single nucleotide variant	NM_005567.4(LGALS3BP):c.206A>T (p.Asn69Ile)	not specified [RCV004412839]	uncertain significance	17	78976003	78976003	Human		name
407492072	CV3452747	single nucleotide variant	NM_005567.4(LGALS3BP):c.251G>A (p.Gly84Asp)	not specified [RCV004642382]	uncertain significance	17	78974813	78974813	Human		name
597641334	CV3696103	single nucleotide variant	NM_005567.4(LGALS3BP):c.281C>T (p.Thr94Met)	not specified [RCV004941675]	likely benign	17	78974783	78974783	Human		name
597641347	CV3696106	single nucleotide variant	NM_005567.4(LGALS3BP):c.154C>G (p.Leu52Val)	not specified [RCV004941678]	uncertain significance	17	78976055	78976055	Human		name
15167714	CV727484	single nucleotide variant	NM_005567.4(LGALS3BP):c.1611C>T (p.Phe537=)	not provided [RCV000882904]	benign	17	78971723	78971723	Human		name
15167833	CV727485	single nucleotide variant	NM_005567.4(LGALS3BP):c.1107C>T (p.His369=)	not provided [RCV000882929]	benign	17	78972227	78972227	Human		name
156253847	CV2209596	single nucleotide variant	NM_005567.4(LGALS3BP):c.484C>A (p.Gln162Lys)	not specified [RCV004093693]	uncertain significance	17	78973115	78973115	Human		name
156248543	CV2215447	single nucleotide variant	NM_005567.4(LGALS3BP):c.817G>A (p.Ala273Thr)	not specified [RCV004089246]	likely benign	17	78972517	78972517	Human		name
155909428	CV2307277	single nucleotide variant	NM_005567.4(LGALS3BP):c.430G>T (p.Gly144Cys)	not specified [RCV004159731]	uncertain significance	17	78973169	78973169	Human		name
156217004	CV2348085	single nucleotide variant	NM_005567.4(LGALS3BP):c.336C>G (p.Asn112Lys)	not specified [RCV004197765]	uncertain significance	17	78974728	78974728	Human		name
156391441	CV2385360	single nucleotide variant	NM_005567.4(LGALS3BP):c.460G>A (p.Asp154Asn)	not specified [RCV004230633]	uncertain significance	17	78973139	78973139	Human		name
329356107	CV2430583	single nucleotide variant	NM_005567.4(LGALS3BP):c.304G>A (p.Asp102Asn)	not specified [RCV004253780]	likely benign	17	78974760	78974760	Human		name
329381713	CV2441507	single nucleotide variant	NM_005567.4(LGALS3BP):c.851C>T (p.Ala284Val)	not specified [RCV004257298]	uncertain significance	17	78972483	78972483	Human		name
329366403	CV2445708	single nucleotide variant	NM_005567.4(LGALS3BP):c.906C>A (p.Asp302Glu)	not specified [RCV004259778]	uncertain significance	17	78972428	78972428	Human		name
329353370	CV2468967	single nucleotide variant	NM_005567.4(LGALS3BP):c.997C>T (p.Arg333Cys)	not specified [RCV004274233]	uncertain significance	17	78972337	78972337	Human		name
401892420	CV2781918	single nucleotide variant	NM_005567.4(LGALS3BP):c.998G>A (p.Arg333His)	not specified [RCV004357161]	uncertain significance	17	78972336	78972336	Human		name
405817830	CV3280333	single nucleotide variant	NM_005567.4(LGALS3BP):c.479A>C (p.Asn160Thr)	not specified [RCV004412840]	uncertain significance	17	78973120	78973120	Human		name
405817832	CV3280335	single nucleotide variant	NM_005567.4(LGALS3BP):c.649A>G (p.Ile217Val)	not specified [RCV004412842]	uncertain significance	17	78972685	78972685	Human		name
405817834	CV3280337	single nucleotide variant	NM_005567.4(LGALS3BP):c.824T>A (p.Leu275Gln)	not specified [RCV004412844]	uncertain significance	17	78972510	78972510	Human		name
405817835	CV3280338	single nucleotide variant	NM_005567.4(LGALS3BP):c.952G>A (p.Glu318Lys)	not specified [RCV004412845]	uncertain significance	17	78972382	78972382	Human		name
405817836	CV3280339	single nucleotide variant	NM_005567.4(LGALS3BP):c.996G>C (p.Glu332Asp)	not specified [RCV004412846]	uncertain significance	17	78972338	78972338	Human		name
407492085	CV3452751	single nucleotide variant	NM_005567.4(LGALS3BP):c.869T>C (p.Leu290Ser)	not specified [RCV004642385]	uncertain significance	17	78972465	78972465	Human		name
597641322	CV3696101	single nucleotide variant	NM_005567.4(LGALS3BP):c.447C>G (p.Ser149Arg)	not specified [RCV004941673]	uncertain significance	17	78973152	78973152	Human		name
597641364	CV3696110	single nucleotide variant	NM_005567.4(LGALS3BP):c.422A>G (p.Glu141Gly)	not specified [RCV004941681]	uncertain significance	17	78973177	78973177	Human		name
598236734	CV3984456	single nucleotide variant	NM_005567.4(LGALS3BP):c.749T>C (p.Leu250Pro)	not specified [RCV005363928]	uncertain significance	17	78972585	78972585	Human		name
598260165	CV3984457	single nucleotide variant	NM_005567.4(LGALS3BP):c.934G>A (p.Asp312Asn)	not specified [RCV005347570]	uncertain significance	17	78972400	78972400	Human		name
156266375	CV2299422	single nucleotide variant	NM_005567.4(LGALS3BP):c.1208C>T (p.Thr403Ile)	not specified [RCV004154506]	uncertain significance	17	78972126	78972126	Human		name
156298014	CV2310577	single nucleotide variant	NM_005567.4(LGALS3BP):c.1414C>A (p.Gln472Lys)	not specified [RCV004163594]	uncertain significance	17	78971920	78971920	Human		name
156165594	CV2315180	single nucleotide variant	NM_005567.4(LGALS3BP):c.1541G>A (p.Arg514His)	not specified [RCV004165353]	uncertain significance	17	78971793	78971793	Human		name
156275586	CV2330682	single nucleotide variant	NM_005567.4(LGALS3BP):c.1646A>C (p.Asp549Ala)	not specified [RCV004185752]	uncertain significance	17	78971688	78971688	Human		name
156387605	CV2372797	single nucleotide variant	NM_005567.4(LGALS3BP):c.1348C>A (p.Pro450Thr)	not specified [RCV004221982]	uncertain significance	17	78971986	78971986	Human		name
155999359	CV2396408	single nucleotide variant	NM_005567.4(LGALS3BP):c.1600G>A (p.Val534Ile)	not specified [RCV004242127]	uncertain significance	17	78971734	78971734	Human		name
401761600	CV2702408	single nucleotide variant	NM_005567.4(LGALS3BP):c.1688C>T (p.Ala563Val)	not specified [RCV004316924]	uncertain significance	17	78971646	78971646	Human		name
401742931	CV2715353	single nucleotide variant	NM_005567.4(LGALS3BP):c.1747G>T (p.Gly583Cys)	not specified [RCV004324685]	uncertain significance	17	78971587	78971587	Human		name
401754410	CV2717380	single nucleotide variant	NM_005567.4(LGALS3BP):c.1274C>T (p.Ala425Val)	not specified [RCV004330215]	uncertain significance	17	78972060	78972060	Human		name
405817826	CV3280329	single nucleotide variant	NM_005567.4(LGALS3BP):c.1105C>T (p.His369Tyr)	not specified [RCV004412836]	uncertain significance	17	78972229	78972229	Human		name
405817827	CV3280330	single nucleotide variant	NM_005567.4(LGALS3BP):c.1538A>C (p.Asp513Ala)	not specified [RCV004412837]	uncertain significance	17	78971796	78971796	Human		name
405817828	CV3280331	single nucleotide variant	NM_005567.4(LGALS3BP):c.1606G>A (p.Asp536Asn)	not specified [RCV004412838]	uncertain significance	17	78971728	78971728	Human		name
407492080	CV3452750	single nucleotide variant	NM_005567.4(LGALS3BP):c.1028T>C (p.Val343Ala)	not specified [RCV004642384]	uncertain significance	17	78972306	78972306	Human		name
407492089	CV3452752	single nucleotide variant	NM_005567.4(LGALS3BP):c.1628C>A (p.Ala543Glu)	not specified [RCV004642386]	uncertain significance	17	78971706	78971706	Human		name
597641329	CV3696102	single nucleotide variant	NM_005567.4(LGALS3BP):c.1276C>T (p.Arg426Trp)	not specified [RCV004941674]	uncertain significance	17	78972058	78972058	Human		name
597641354	CV3696107	single nucleotide variant	NM_005567.4(LGALS3BP):c.1721G>A (p.Arg574His)	not specified [RCV004941679]	uncertain significance	17	78971613	78971613	Human		name
597641360	CV3696108	single nucleotide variant	NM_005567.4(LGALS3BP):c.1624G>T (p.Ala542Ser)	not specified [RCV004941680]	uncertain significance	17	78971710	78971710	Human		name
597795717	CV3696109	single nucleotide variant	NM_005567.4(LGALS3BP):c.1685C>T (p.Pro562Leu)	not specified [RCV004934945]	uncertain significance	17	78971649	78971649	Human		name
597641369	CV3696111	single nucleotide variant	NM_005567.4(LGALS3BP):c.1081T>G (p.Phe361Val)	not specified [RCV004941682]	uncertain significance	17	78972253	78972253	Human		name
598236738	CV3984458	single nucleotide variant	NM_005567.4(LGALS3BP):c.1277G>A (p.Arg426Gln)	not specified [RCV005363929]	uncertain significance	17	78972057	78972057	Human		name
598260171	CV3984459	single nucleotide variant	NM_005567.4(LGALS3BP):c.1013A>G (p.Glu338Gly)	not specified [RCV005347571]	uncertain significance	17	78972321	78972321	Human		name
15181577	CV715762	single nucleotide variant	NM_005567.4(LGALS3BP):c.1307G>C (p.Arg436Pro)	not provided [RCV000974424]	benign	17	78972027	78972027	Human		name
15201859	CV756189	single nucleotide variant	NM_005567.4(LGALS3BP):c.1178G>A (p.Arg393Gln)	not provided [RCV000913267]	likely benign	17	78972156	78972156	Human		name

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