Bmx Variant Search Result - Rat Genome Database

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39 records found for search term Bmx

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401905030	CV2823926	single nucleotide variant	NM_203281.3(BMX):c.1611+6C>A	not provided [RCV003441044]	likely benign	X	15542204	15542204	Human		name
15103968	CV760878	single nucleotide variant	NM_203281.3(BMX):c.1796-9G>C	not provided [RCV000915265]	benign	X	15549831	15549831	Human		name
8587295	CV121922	single nucleotide variant	NM_203281.2(BMX):c.326-2247C>T	Lung cancer [RCV000102442]	uncertain significance	X	15513865	15513865	Human		name
15146357	CV743260	single nucleotide variant	NM_203281.3(BMX):c.264T>A (p.Leu88=)	not provided [RCV000900312]	benign	X	15511457	15511457	Human		name
8637812	CV93038	single nucleotide variant	NM_203281.2(BMX):c.516G>A (p.Lys172=)	Malignant melanoma [RCV000073136]	not provided	X	15522351	15522351	Human		name
401905029	CV2823925	single nucleotide variant	NM_203281.3(BMX):c.1242A>G (p.Arg414=)	not provided [RCV003441043]	likely benign	X	15537153	15537153	Human		name
598162573	CV3946201	single nucleotide variant	NM_203281.3(BMX):c.1020T>C (p.Asn340=)	not specified [RCV005307253]	likely benign	X	15534212	15534212	Human		name
15123298	CV743262	single nucleotide variant	NM_203281.3(BMX):c.1602C>T (p.His534=)	not provided [RCV000896388]	benign	X	15542189	15542189	Human		name
156118971	CV2219226	single nucleotide variant	NM_203281.3(BMX):c.343C>T (p.His115Tyr)	not specified [RCV004093486]	uncertain significance	X	15516129	15516129	Human		name
156267945	CV2329722	single nucleotide variant	NM_203281.3(BMX):c.425G>A (p.Gly142Glu)	not specified [RCV004180826]	uncertain significance	X	15516211	15516211	Human		name
155923365	CV2347492	single nucleotide variant	NM_203281.3(BMX):c.635G>C (p.Ser212Thr)	not specified [RCV004200441]	likely benign	X	15522470	15522470	Human		name
329397099	CV2459919	single nucleotide variant	NM_203281.3(BMX):c.472G>A (p.Glu158Lys)	not specified [RCV004279410]	uncertain significance	X	15517955	15517955	Human		name
329350315	CV2464400	single nucleotide variant	NM_203281.3(BMX):c.542A>G (p.Lys181Arg)	not specified [RCV004276335]	likely benign	X	15522377	15522377	Human		name
401743756	CV2677713	single nucleotide variant	NM_203281.3(BMX):c.904T>G (p.Ser302Ala)	not specified [RCV004291794]	uncertain significance	X	15529992	15529992	Human		name
405763113	CV3291320	single nucleotide variant	NM_203281.3(BMX):c.382G>T (p.Gly128Trp)	not specified [RCV004433971]	uncertain significance	X	15516168	15516168	Human		name
405763119	CV3291321	single nucleotide variant	NM_203281.3(BMX):c.464C>T (p.Ala155Val)	not specified [RCV004433972]	uncertain significance	X	15517947	15517947	Human		name
405763125	CV3291322	single nucleotide variant	NM_203281.3(BMX):c.640G>A (p.Ala214Thr)	not specified [RCV004433973]	uncertain significance	X	15522475	15522475	Human		name
597690719	CV3643110	single nucleotide variant	NM_203281.3(BMX):c.662A>G (p.Lys221Arg)	not specified [RCV004887614]	uncertain significance	X	15522497	15522497	Human		name
597690729	CV3643111	single nucleotide variant	NM_203281.3(BMX):c.559T>C (p.Ser187Pro)	not specified [RCV004887615]	uncertain significance	X	15522394	15522394	Human		name
597719334	CV3643115	single nucleotide variant	NM_203281.3(BMX):c.392T>G (p.Leu131Arg)	not specified [RCV004887619]	uncertain significance	X	15516178	15516178	Human		name
597719342	CV3643116	single nucleotide variant	NM_203281.3(BMX):c.352G>C (p.Val118Leu)	not specified [RCV004887620]	uncertain significance	X	15516138	15516138	Human		name
598162563	CV3946198	single nucleotide variant	NM_203281.3(BMX):c.881A>T (p.Tyr294Phe)	not specified [RCV005307251]	uncertain significance	X	15526092	15526092	Human		name
598250411	CV3946199	single nucleotide variant	NM_203281.3(BMX):c.523C>T (p.Arg175Trp)	not specified [RCV005298336]	uncertain significance	X	15522358	15522358	Human		name
15161499	CV743261	single nucleotide variant	NM_203281.3(BMX):c.641C>T (p.Ala214Val)	not provided [RCV000903359]	benign	X	15522476	15522476	Human		name
8637813	CV93039	single nucleotide variant	NM_203281.2(BMX):c.546G>A (p.Met182Ile)	Malignant melanoma [RCV000073137]	not provided	X	15522381	15522381	Human		name
156232304	CV2245150	single nucleotide variant	NM_203281.3(BMX):c.1711G>A (p.Gly571Arg)	not specified [RCV004106935]	uncertain significance	X	15546837	15546837	Human		name
156176839	CV2258131	single nucleotide variant	NM_203281.3(BMX):c.1951G>A (p.Glu651Lys)	not specified [RCV004121519]	uncertain significance	X	15549995	15549995	Human		name
156076096	CV2331782	single nucleotide variant	NM_203281.3(BMX):c.1408C>G (p.Pro470Ala)	not specified [RCV004184403]	uncertain significance	X	15541995	15541995	Human		name
329350186	CV2441763	single nucleotide variant	NM_203281.3(BMX):c.1499A>T (p.Tyr500Phe)	not specified [RCV004261975]	uncertain significance	X	15542086	15542086	Human		name
401856678	CV2755162	single nucleotide variant	NM_203281.3(BMX):c.1897C>T (p.Arg633Trp)	not specified [RCV004335310]	uncertain significance	X	15549941	15549941	Human		name
405763102	CV3291318	single nucleotide variant	NM_203281.3(BMX):c.1711G>C (p.Gly571Arg)	not specified [RCV004433969]	uncertain significance	X	15546837	15546837	Human		name
405763108	CV3291319	single nucleotide variant	NM_203281.3(BMX):c.1862T>C (p.Val621Ala)	not specified [RCV004433970]	uncertain significance	X	15549906	15549906	Human		name
407480425	CV3424024	single nucleotide variant	NM_203281.3(BMX):c.1198C>T (p.Pro400Ser)	not specified [RCV004600572]	uncertain significance	X	15536403	15536403	Human		name
597690739	CV3643113	single nucleotide variant	NM_203281.3(BMX):c.1421A>G (p.Lys474Arg)	not specified [RCV004887617]	uncertain significance	X	15542008	15542008	Human		name
597690748	CV3643114	single nucleotide variant	NM_203281.3(BMX):c.1033A>G (p.Thr345Ala)	not specified [RCV004887618]	uncertain significance	X	15534225	15534225	Human		name
598250403	CV3946197	single nucleotide variant	NM_203281.3(BMX):c.1371C>A (p.Phe457Leu)	not specified [RCV005298335]	uncertain significance	X	15537282	15537282	Human		name
598162568	CV3946200	single nucleotide variant	NM_203281.3(BMX):c.1330G>A (p.Val444Ile)	not specified [RCV005307252]	uncertain significance	X	15537241	15537241	Human		name
598250418	CV3946202	single nucleotide variant	NM_203281.3(BMX):c.1186G>A (p.Ala396Thr)	not specified [RCV005298337]	uncertain significance	X	15536391	15536391	Human		name
598162579	CV3946203	single nucleotide variant	NM_203281.3(BMX):c.1522C>T (p.Leu508Phe)	not specified [RCV005307254]	uncertain significance	X	15542109	15542109	Human		name

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