Sh3bp1 Variant Search Result - Rat Genome Database

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79 records found for search term Sh3bp1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15114894	CV780166	single nucleotide variant	NM_018957.6(SH3BP1):c.103-7T>C	not provided [RCV000961758]	benign	22	37641367	37641367	Human		name
15202912	CV760764	single nucleotide variant	NM_018957.6(SH3BP1):c.1599-9C>T	not provided [RCV000913610]	likely benign	22	37653770	37653770	Human		name
597695860	CV3606040	single nucleotide variant	NM_018957.6(SH3BP1):c.19C>T (p.His7Tyr)	not specified [RCV004859341]	uncertain significance	22	37639806	37639806	Human		name
15112107	CV717443	single nucleotide variant	NM_018957.6(SH3BP1):c.123G>A (p.Pro41=)	not provided [RCV000961238]	benign	22	37641394	37641394	Human		name
155956936	CV2387378	single nucleotide variant	NM_018957.6(SH3BP1):c.73G>A (p.Ala25Thr)	not specified [RCV004240247]	uncertain significance	22	37641139	37641139	Human		name
405708283	CV3317949	single nucleotide variant	NM_018957.6(SH3BP1):c.43A>T (p.Thr15Ser)	not specified [RCV004448113]	uncertain significance	22	37639830	37639830	Human		name
405708296	CV3317951	single nucleotide variant	NM_018957.6(SH3BP1):c.85G>A (p.Gly29Ser)	not specified [RCV004448115]	uncertain significance	22	37641151	37641151	Human		name
156264062	CV2282628	single nucleotide variant	NM_018957.6(SH3BP1):c.187G>C (p.Ala63Pro)	not specified [RCV004135187]	uncertain significance	22	37641458	37641458	Human		name
156151346	CV2318772	single nucleotide variant	NM_018957.6(SH3BP1):c.200A>G (p.Lys67Arg)	not specified [RCV004175694]	uncertain significance	22	37641471	37641471	Human		name
156080601	CV2368712	single nucleotide variant	NM_018957.6(SH3BP1):c.202C>T (p.Arg68Trp)	not specified [RCV004214598]	uncertain significance	22	37641473	37641473	Human		name
401926022	CV2822180	single nucleotide variant	NM_018957.6(SH3BP1):c.1182G>A (p.Glu394=)	not provided [RCV003437558]	likely benign	22	37647504	37647504	Human		name
405708180	CV3317934	single nucleotide variant	NM_018957.6(SH3BP1):c.113G>A (p.Arg38Gln)	not specified [RCV004448098]	uncertain significance	22	37641384	37641384	Human		name
405708205	CV3317938	single nucleotide variant	NM_018957.6(SH3BP1):c.154C>T (p.Arg52Trp)	not specified [RCV004448102]	uncertain significance	22	37641425	37641425	Human		name
405708239	CV3317942	single nucleotide variant	NM_018957.6(SH3BP1):c.175G>T (p.Gly59Cys)	not specified [RCV004448106]	uncertain significance	22	37641446	37641446	Human		name
405708242	CV3317943	single nucleotide variant	NM_018957.6(SH3BP1):c.187G>A (p.Ala63Thr)	not specified [RCV004448107]	uncertain significance	22	37641458	37641458	Human		name
597695819	CV3606036	single nucleotide variant	NM_018957.6(SH3BP1):c.209A>C (p.Lys70Thr)	not specified [RCV004859337]	uncertain significance	22	37642540	37642540	Human		name
598240073	CV3917767	single nucleotide variant	NM_018957.6(SH3BP1):c.112C>T (p.Arg38Trp)	not specified [RCV005276133]	uncertain significance	22	37641383	37641383	Human		name
155920015	CV2209838	single nucleotide variant	NM_018957.6(SH3BP1):c.527C>T (p.Pro176Leu)	not specified [RCV004076301]	uncertain significance	22	37643697	37643697	Human		name
156052778	CV2246352	single nucleotide variant	NM_018957.6(SH3BP1):c.850G>A (p.Glu284Lys)	not specified [RCV004107792]	uncertain significance	22	37645436	37645436	Human		name
156333065	CV2270499	single nucleotide variant	NM_018957.6(SH3BP1):c.362G>A (p.Arg121Lys)	not specified [RCV004137458]	uncertain significance	22	37642972	37642972	Human		name
156273168	CV2283807	single nucleotide variant	NM_018957.6(SH3BP1):c.796A>G (p.Thr266Ala)	not specified [RCV004142323]	likely benign	22	37645382	37645382	Human		name
155989239	CV2371915	single nucleotide variant	NM_018957.6(SH3BP1):c.986C>T (p.Ser329Leu)	not specified [RCV004221601]	uncertain significance	22	37646879	37646879	Human		name
156049607	CV2391097	single nucleotide variant	NM_018957.6(SH3BP1):c.889G>A (p.Val297Ile)	not specified [RCV004235082]	uncertain significance	22	37645475	37645475	Human		name
155996642	CV2393211	single nucleotide variant	NM_018957.6(SH3BP1):c.860G>A (p.Arg287Gln)	not specified [RCV004226682]	uncertain significance	22	37645446	37645446	Human		name
156269125	CV2398543	single nucleotide variant	NM_018957.6(SH3BP1):c.376C>G (p.Pro126Ala)	not specified [RCV004237862]	uncertain significance	22	37642986	37642986	Human		name
401719656	CV2701220	single nucleotide variant	NM_018957.6(SH3BP1):c.742G>T (p.Ala248Ser)	not specified [RCV004309794]	uncertain significance	22	37644924	37644924	Human		name
405708290	CV3317950	single nucleotide variant	NM_018957.6(SH3BP1):c.797C>T (p.Thr266Ile)	not specified [RCV004448114]	uncertain significance	22	37645383	37645383	Human		name
405708303	CV3317952	single nucleotide variant	NM_018957.6(SH3BP1):c.880G>A (p.Glu294Lys)	not specified [RCV004448116]	uncertain significance	22	37645466	37645466	Human		name
407490446	CV3484206	single nucleotide variant	NM_018957.6(SH3BP1):c.361A>G (p.Arg121Gly)	not specified [RCV004666315]	uncertain significance	22	37642971	37642971	Human		name
597695850	CV3606039	single nucleotide variant	NM_018957.6(SH3BP1):c.700C>G (p.Gln234Glu)	not specified [RCV004859340]	uncertain significance	22	37644882	37644882	Human		name
598240050	CV3917763	single nucleotide variant	NM_018957.6(SH3BP1):c.808T>C (p.Phe270Leu)	not specified [RCV005276129]	uncertain significance	22	37645394	37645394	Human		name
598240066	CV3917766	single nucleotide variant	NM_018957.6(SH3BP1):c.451G>A (p.Asp151Asn)	not specified [RCV005276132]	uncertain significance	22	37643152	37643152	Human		name
156088210	CV2201967	single nucleotide variant	NM_018957.6(SH3BP1):c.1331T>G (p.Leu444Arg)	not specified [RCV004075895]	uncertain significance	22	37650166	37650166	Human		name
156113411	CV2224818	single nucleotide variant	NM_018957.6(SH3BP1):c.1703C>A (p.Pro568Gln)	not specified [RCV004092919]	uncertain significance	22	37655281	37655281	Human		name
156114795	CV2225191	single nucleotide variant	NM_018957.6(SH3BP1):c.1715G>A (p.Arg572Gln)	not specified [RCV004094992]	uncertain significance	22	37655293	37655293	Human		name
155989947	CV2259751	single nucleotide variant	NM_018957.6(SH3BP1):c.1742C>T (p.Ser581Phe)	not specified [RCV004116761]	uncertain significance	22	37655320	37655320	Human		name
155946236	CV2266026	single nucleotide variant	NM_018957.6(SH3BP1):c.1177C>G (p.Pro393Ala)	not specified [RCV004126847]	uncertain significance	22	37647499	37647499	Human		name
156018835	CV2272399	single nucleotide variant	NM_018957.6(SH3BP1):c.1700G>A (p.Arg567His)	not specified [RCV004133323]	uncertain significance	22	37655278	37655278	Human		name
156028002	CV2278487	single nucleotide variant	NM_018957.6(SH3BP1):c.1511T>C (p.Val504Ala)	not specified [RCV004132929]	uncertain significance	22	37650638	37650638	Human		name
156277668	CV2284859	single nucleotide variant	NM_018957.6(SH3BP1):c.1766C>A (p.Ala589Asp)	not specified [RCV004143317]	uncertain significance	22	37655344	37655344	Human		name
156282292	CV2318602	single nucleotide variant	NM_018957.6(SH3BP1):c.1346T>C (p.Val449Ala)	not specified [RCV004173502]	uncertain significance	22	37650181	37650181	Human		name
155901160	CV2345748	single nucleotide variant	NM_018957.6(SH3BP1):c.2083A>T (p.Ser695Cys)	not specified [RCV004205682]	uncertain significance	22	37655661	37655661	Human		name
156000839	CV2383281	single nucleotide variant	NM_018957.6(SH3BP1):c.1606T>C (p.Ser536Pro)	not specified [RCV004222329]	uncertain significance	22	37653786	37653786	Human		name
329359340	CV2435433	single nucleotide variant	NM_018957.6(SH3BP1):c.1135G>C (p.Ala379Pro)	not specified [RCV004253085]	uncertain significance	22	37647457	37647457	Human		name
401733480	CV2682126	single nucleotide variant	NM_018957.6(SH3BP1):c.1776G>C (p.Leu592Phe)	not specified [RCV004290181]	uncertain significance	22	37655354	37655354	Human		name
401722567	CV2703416	single nucleotide variant	NM_018957.6(SH3BP1):c.1400C>G (p.Thr467Ser)	not specified [RCV004317616]	uncertain significance	22	37650235	37650235	Human		name
401892594	CV2782258	single nucleotide variant	NM_018957.6(SH3BP1):c.1897C>T (p.Arg633Cys)	not specified [RCV004359224]	uncertain significance	22	37655475	37655475	Human		name
405708171	CV3317933	single nucleotide variant	NM_018957.6(SH3BP1):c.1139G>A (p.Arg380Gln)	not specified [RCV004448097]	uncertain significance	22	37647461	37647461	Human		name
405708186	CV3317935	single nucleotide variant	NM_018957.6(SH3BP1):c.1178C>G (p.Pro393Arg)	not specified [RCV004448099]	uncertain significance	22	37647500	37647500	Human		name
405708191	CV3317936	single nucleotide variant	NM_018957.6(SH3BP1):c.1393G>T (p.Ala465Ser)	not specified [RCV004448100]	uncertain significance	22	37650228	37650228	Human		name
405708197	CV3317937	single nucleotide variant	NM_018957.6(SH3BP1):c.1510G>A (p.Val504Met)	not specified [RCV004448101]	uncertain significance	22	37650637	37650637	Human		name
405708213	CV3317939	single nucleotide variant	NM_018957.6(SH3BP1):c.1650T>A (p.Ser550Arg)	not specified [RCV004448103]	uncertain significance	22	37653830	37653830	Human		name
405708221	CV3317940	single nucleotide variant	NM_018957.6(SH3BP1):c.1730C>G (p.Pro577Arg)	not specified [RCV004448104]	uncertain significance	22	37655308	37655308	Human		name
405708231	CV3317941	single nucleotide variant	NM_018957.6(SH3BP1):c.1732C>T (p.Pro578Ser)	not specified [RCV004448105]	uncertain significance	22	37655310	37655310	Human		name
405708254	CV3317944	single nucleotide variant	NM_018957.6(SH3BP1):c.1894C>T (p.Arg632Trp)	not specified [RCV004448108]	uncertain significance	22	37655472	37655472	Human		name
405708259	CV3317945	single nucleotide variant	NM_018957.6(SH3BP1):c.1895G>A (p.Arg632Gln)	not specified [RCV004448109]	uncertain significance	22	37655473	37655473	Human		name
405708265	CV3317946	single nucleotide variant	NM_018957.6(SH3BP1):c.1898G>A (p.Arg633His)	not specified [RCV004448110]	uncertain significance	22	37655476	37655476	Human		name
405708663	CV3317947	single nucleotide variant	NM_018957.6(SH3BP1):c.1901A>G (p.Gln634Arg)	not specified [RCV004448111]	uncertain significance	22	37655479	37655479	Human		name
405708277	CV3317948	single nucleotide variant	NM_018957.6(SH3BP1):c.2065C>T (p.Pro689Ser)	not specified [RCV004448112]	uncertain significance	22	37655643	37655643	Human		name
407492922	CV3484200	single nucleotide variant	NM_018957.6(SH3BP1):c.1562C>A (p.Pro521Gln)	not specified [RCV004667258]	uncertain significance	22	37650689	37650689	Human		name
407490434	CV3484201	single nucleotide variant	NM_018957.6(SH3BP1):c.1223G>A (p.Arg408Gln)	not specified [RCV004666311]	uncertain significance	22	37648342	37648342	Human		name
407492927	CV3484202	single nucleotide variant	NM_018957.6(SH3BP1):c.1253T>A (p.Met418Lys)	not specified [RCV004667259]	uncertain significance	22	37648372	37648372	Human		name
407490437	CV3484203	single nucleotide variant	NM_018957.6(SH3BP1):c.1168C>T (p.Arg390Cys)	not specified [RCV004666312]	uncertain significance	22	37647490	37647490	Human		name
407490440	CV3484204	single nucleotide variant	NM_018957.6(SH3BP1):c.1730C>A (p.Pro577His)	not specified [RCV004666313]	uncertain significance	22	37655308	37655308	Human		name
407490443	CV3484205	single nucleotide variant	NM_018957.6(SH3BP1):c.1733C>G (p.Pro578Arg)	not specified [RCV004666314]	uncertain significance	22	37655311	37655311	Human		name
597695767	CV3606031	single nucleotide variant	NM_018957.6(SH3BP1):c.1823G>T (p.Arg608Leu)	not specified [RCV004859332]	uncertain significance	22	37655401	37655401	Human		name
597695777	CV3606032	single nucleotide variant	NM_018957.6(SH3BP1):c.1844G>A (p.Arg615Gln)	not specified [RCV004859333]	uncertain significance	22	37655422	37655422	Human		name
597695788	CV3606033	single nucleotide variant	NM_018957.6(SH3BP1):c.2082G>T (p.Arg694Ser)	not specified [RCV004859334]	uncertain significance	22	37655660	37655660	Human		name
597695800	CV3606034	single nucleotide variant	NM_018957.6(SH3BP1):c.1931C>T (p.Pro644Leu)	not specified [RCV004859335]	uncertain significance	22	37655509	37655509	Human		name
597695827	CV3606037	single nucleotide variant	NM_018957.6(SH3BP1):c.2074C>T (p.Arg692Cys)	not specified [RCV004859338]	uncertain significance	22	37655652	37655652	Human		name
597695839	CV3606038	single nucleotide variant	NM_018957.6(SH3BP1):c.1913C>T (p.Ser638Leu)	not specified [RCV004859339]	uncertain significance	22	37655491	37655491	Human		name
597695871	CV3606041	single nucleotide variant	NM_018957.6(SH3BP1):c.1514C>G (p.Pro505Arg)	not specified [RCV004859342]	uncertain significance	22	37650641	37650641	Human		name
598240037	CV3917760	single nucleotide variant	NM_018957.6(SH3BP1):c.1823G>A (p.Arg608His)	not specified [RCV005276127]	uncertain significance	22	37655401	37655401	Human		name
598240042	CV3917761	single nucleotide variant	NM_018957.6(SH3BP1):c.1999G>A (p.Ala667Thr)	not specified [RCV005276128]	uncertain significance	22	37655577	37655577	Human		name
598198911	CV3917762	single nucleotide variant	NM_018957.6(SH3BP1):c.1997G>C (p.Gly666Ala)	not specified [RCV005268322]	uncertain significance	22	37655575	37655575	Human		name
598240059	CV3917765	single nucleotide variant	NM_018957.6(SH3BP1):c.1471A>G (p.Ser491Gly)	not specified [RCV005276131]	uncertain significance	22	37650598	37650598	Human		name
598240078	CV3917768	single nucleotide variant	NM_018957.6(SH3BP1):c.1772C>T (p.Pro591Leu)	not specified [RCV005276134]	uncertain significance	22	37655350	37655350	Human		name
598240085	CV3917769	single nucleotide variant	NM_018957.6(SH3BP1):c.1940C>T (p.Pro647Leu)	not specified [RCV005276135]	uncertain significance	22	37655518	37655518	Human		name
598240092	CV3917770	single nucleotide variant	NM_018957.6(SH3BP1):c.1650T>G (p.Ser550Arg)	not specified [RCV005276136]	uncertain significance	22	37653830	37653830	Human		name

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