Slitrk5 Variant Search Result - Rat Genome Database

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108 records found for search term Slitrk5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156236423	CV2239014	single nucleotide variant	NM_001384609.1(SLITRK5):c.19C>T (p.Pro7Ser)	not specified [RCV004109896]	uncertain significance	13	87675407	87675407	Human		name
401901953	CV2813960	single nucleotide variant	NM_001384609.1(SLITRK5):c.823T>C (p.Leu275=)	not provided [RCV003393369]	likely benign	13	87676211	87676211	Human		name
407452244	CV3477513	single nucleotide variant	NM_001384609.1(SLITRK5):c.86C>T (p.Ala29Val)	not specified [RCV004683949]	uncertain significance	13	87675474	87675474	Human		name
597726304	CV3603403	single nucleotide variant	NM_001384609.1(SLITRK5):c.40C>A (p.Leu14Ile)	not specified [RCV004862547]	uncertain significance	13	87675428	87675428	Human		name
329387833	CV2446831	single nucleotide variant	NM_001384609.1(SLITRK5):c.191G>C (p.Ser64Thr)	not specified [RCV004257686]	uncertain significance	13	87675579	87675579	Human		name
401748388	CV2698374	single nucleotide variant	NM_001384609.1(SLITRK5):c.126T>G (p.Asp42Glu)	not specified [RCV004304913]	uncertain significance	13	87675514	87675514	Human		name
401878140	CV2777720	single nucleotide variant	NM_001384609.1(SLITRK5):c.122T>C (p.Ile41Thr)	not specified [RCV004345556]	uncertain significance	13	87675510	87675510	Human		name
405286419	CV3192762	single nucleotide variant	NM_001384609.1(SLITRK5):c.2760G>A (p.Pro920=)	SLITRK5-related disorder [RCV003981506]	likely benign	13	87678148	87678148	Human		name , trait , alternate_id
405276720	CV3198635	single nucleotide variant	NM_001384609.1(SLITRK5):c.1866G>C (p.Thr622=)	SLITRK5-related disorder [RCV003903962]	likely benign	13	87677254	87677254	Human		name , trait , alternate_id
405262403	CV3200251	single nucleotide variant	NM_001384609.1(SLITRK5):c.1317C>T (p.His439=)	SLITRK5-related disorder [RCV003967290]	likely benign	13	87676705	87676705	Human		name , trait , alternate_id
405785784	CV3333184	single nucleotide variant	NM_001384609.1(SLITRK5):c.296A>G (p.Asn99Ser)	not specified [RCV004459514]	uncertain significance	13	87675684	87675684	Human		name
407494110	CV3477507	single nucleotide variant	NM_001384609.1(SLITRK5):c.247A>G (p.Ile83Val)	not specified [RCV004667549]	likely benign	13	87675635	87675635	Human		name
408365888	CV3512046	single nucleotide variant	NM_001384609.1(SLITRK5):c.2464A>C (p.Arg822=)	SLITRK5-related disorder [RCV004755394]	likely benign	13	87677852	87677852	Human		name , trait , alternate_id
597778032	CV3603401	single nucleotide variant	NM_001384609.1(SLITRK5):c.284G>A (p.Arg95His)	not specified [RCV004873179]	uncertain significance	13	87675672	87675672	Human		name
597726312	CV3603404	single nucleotide variant	NM_001384609.1(SLITRK5):c.158C>T (p.Pro53Leu)	not specified [RCV004862548]	uncertain significance	13	87675546	87675546	Human		name
597778043	CV3603410	single nucleotide variant	NM_001384609.1(SLITRK5):c.215G>A (p.Ser72Asn)	not specified [RCV004873182]	uncertain significance	13	87675603	87675603	Human		name
598270311	CV3918551	single nucleotide variant	NM_001384609.1(SLITRK5):c.123C>G (p.Ile41Met)	not specified [RCV005282129]	uncertain significance	13	87675511	87675511	Human		name
598237878	CV3918553	single nucleotide variant	NM_001384609.1(SLITRK5):c.100G>A (p.Val34Ile)	not specified [RCV005275739]	uncertain significance	13	87675488	87675488	Human		name
15185465	CV702738	single nucleotide variant	NM_001384609.1(SLITRK5):c.2103C>T (p.Ser701=)	not provided [RCV000952992]	benign	13	87677491	87677491	Human		name
15104788	CV725528	single nucleotide variant	NM_001384609.1(SLITRK5):c.1299G>C (p.Thr433=)	not provided [RCV000892953]	benign	13	87676687	87676687	Human		name
42723388	CV984389	single nucleotide variant	NM_001384609.1(SLITRK5):c.175G>T (p.Gly59Cys)	Autism spectrum disorder [RCV001291194]	association	13	87675563	87675563	Human	2	name
156123702	CV2234079	single nucleotide variant	NM_001384609.1(SLITRK5):c.443C>A (p.Thr148Asn)	not specified [RCV004106185]	uncertain significance	13	87675831	87675831	Human		name
156150593	CV2235057	single nucleotide variant	NM_001384609.1(SLITRK5):c.568T>C (p.Ser190Pro)	not specified [RCV004113239]	uncertain significance	13	87675956	87675956	Human		name
155928193	CV2281039	single nucleotide variant	NM_001384609.1(SLITRK5):c.652G>A (p.Val218Met)	not specified [RCV004145527]	uncertain significance	13	87676040	87676040	Human		name
156395630	CV2329293	single nucleotide variant	NM_001384609.1(SLITRK5):c.828C>A (p.Asp276Glu)	not specified [RCV004174030]	uncertain significance	13	87676216	87676216	Human		name
156230480	CV2348683	single nucleotide variant	NM_001384609.1(SLITRK5):c.856A>G (p.Arg286Gly)	not specified [RCV004201099]	uncertain significance	13	87676244	87676244	Human		name
329393014	CV2469171	single nucleotide variant	NM_001384609.1(SLITRK5):c.805C>G (p.Arg269Gly)	not specified [RCV004280529]	uncertain significance	13	87676193	87676193	Human		name
405273421	CV3192270	single nucleotide variant	NM_001384609.1(SLITRK5):c.354G>T (p.Gln118His)	SLITRK5-related disorder [RCV003914726]	likely benign	13	87675742	87675742	Human		name , trait , alternate_id
405785790	CV3333185	single nucleotide variant	NM_001384609.1(SLITRK5):c.441T>G (p.Asp147Glu)	not specified [RCV004459515]	uncertain significance	13	87675829	87675829	Human		name
405785794	CV3333186	single nucleotide variant	NM_001384609.1(SLITRK5):c.497G>A (p.Ser166Asn)	not specified [RCV004459516]	uncertain significance	13	87675885	87675885	Human		name
405785799	CV3333187	single nucleotide variant	NM_001384609.1(SLITRK5):c.508C>T (p.Pro170Ser)	not specified [RCV004459517]	uncertain significance	13	87675896	87675896	Human		name
405785802	CV3333188	single nucleotide variant	NM_001384609.1(SLITRK5):c.623G>A (p.Arg208Gln)	not specified [RCV004459518]	uncertain significance	13	87676011	87676011	Human		name
405785810	CV3333190	single nucleotide variant	NM_001384609.1(SLITRK5):c.971A>T (p.Tyr324Phe)	not specified [RCV004459520]	uncertain significance	13	87676359	87676359	Human		name
407494114	CV3477509	single nucleotide variant	NM_001384609.1(SLITRK5):c.475C>G (p.Gln159Glu)	not specified [RCV004667550]	uncertain significance	13	87675863	87675863	Human		name
408384478	CV3505428	single nucleotide variant	NM_001384609.1(SLITRK5):c.994A>T (p.Lys332Ter)	SLITRK5-related disorder [RCV004731844]	uncertain significance	13	87676382	87676382	Human		name , trait , alternate_id
598270322	CV3918554	single nucleotide variant	NM_001384609.1(SLITRK5):c.583A>C (p.Asn195His)	not specified [RCV005282131]	uncertain significance	13	87675971	87675971	Human		name
42723389	CV984390	single nucleotide variant	NM_001384609.1(SLITRK5):c.976C>T (p.Pro326Ser)	Autism spectrum disorder [RCV001291195]	association	13	87676364	87676364	Human	2	name
156182705	CV2201908	single nucleotide variant	NM_001384609.1(SLITRK5):c.2228C>T (p.Thr743Met)	not specified [RCV004075491]	uncertain significance	13	87677616	87677616	Human		name
156251481	CV2232306	single nucleotide variant	NM_001384609.1(SLITRK5):c.2525A>C (p.Glu842Ala)	not specified [RCV004105081]	uncertain significance	13	87677913	87677913	Human		name
156282105	CV2252379	single nucleotide variant	NM_001384609.1(SLITRK5):c.1753G>A (p.Val585Ile)	not specified [RCV004116223]	uncertain significance	13	87677141	87677141	Human		name
155925828	CV2258630	single nucleotide variant	NM_001384609.1(SLITRK5):c.1130C>T (p.Ala377Val)	not specified [RCV004117888]	uncertain significance	13	87676518	87676518	Human		name
156359088	CV2260985	single nucleotide variant	NM_001384609.1(SLITRK5):c.2023A>C (p.Ile675Leu)	not specified [RCV004125864]	uncertain significance	13	87677411	87677411	Human		name
156166705	CV2270436	single nucleotide variant	NM_001384609.1(SLITRK5):c.2593T>C (p.Cys865Arg)	not specified [RCV004137406]	uncertain significance	13	87677981	87677981	Human		name
155921138	CV2276254	single nucleotide variant	NM_001384609.1(SLITRK5):c.1799A>G (p.Glu600Gly)	not specified [RCV004144014]	uncertain significance	13	87677187	87677187	Human		name
156061625	CV2280444	single nucleotide variant	NM_001384609.1(SLITRK5):c.1195G>C (p.Glu399Gln)	not specified [RCV004140616]	uncertain significance	13	87676583	87676583	Human		name
156291187	CV2296609	single nucleotide variant	NM_001384609.1(SLITRK5):c.2659T>A (p.Tyr887Asn)	not specified [RCV004154670]	uncertain significance	13	87678047	87678047	Human		name
156095906	CV2297406	single nucleotide variant	NM_001384609.1(SLITRK5):c.2364C>G (p.Ser788Arg)	not specified [RCV004153348]	uncertain significance	13	87677752	87677752	Human		name
156253668	CV2311477	single nucleotide variant	NM_001384609.1(SLITRK5):c.2234C>T (p.Ala745Val)	not specified [RCV004168315]	uncertain significance	13	87677622	87677622	Human		name
156175898	CV2317332	single nucleotide variant	NM_001384609.1(SLITRK5):c.1373A>G (p.Asn458Ser)	not specified [RCV004178816]	uncertain significance	13	87676761	87676761	Human		name
156169075	CV2320140	single nucleotide variant	NM_001384609.1(SLITRK5):c.2164G>T (p.Gly722Cys)	not specified [RCV004167981]	uncertain significance	13	87677552	87677552	Human		name
156156101	CV2328845	single nucleotide variant	NM_001384609.1(SLITRK5):c.2642C>T (p.Pro881Leu)	not specified [RCV004178061]	uncertain significance	13	87678030	87678030	Human		name
156113934	CV2349163	single nucleotide variant	NM_001384609.1(SLITRK5):c.2269G>C (p.Gly757Arg)	not specified [RCV004199122]	uncertain significance	13	87677657	87677657	Human		name
156225533	CV2390625	single nucleotide variant	NM_001384609.1(SLITRK5):c.1681C>A (p.His561Asn)	not specified [RCV004239148]	uncertain significance	13	87677069	87677069	Human		name
401733413	CV2685519	single nucleotide variant	NM_001384609.1(SLITRK5):c.2437C>A (p.Leu813Met)	not specified [RCV004294538]	uncertain significance	13	87677825	87677825	Human		name
401748213	CV2696558	single nucleotide variant	NM_001384609.1(SLITRK5):c.2551G>A (p.Ala851Thr)	not specified [RCV004312614]	uncertain significance	13	87677939	87677939	Human		name
401748303	CV2696589	single nucleotide variant	NM_001384609.1(SLITRK5):c.2755C>G (p.Pro919Ala)	not specified [RCV004312623]	uncertain significance	13	87678143	87678143	Human		name
401762600	CV2714204	single nucleotide variant	NM_001384609.1(SLITRK5):c.1585A>G (p.Thr529Ala)	not specified [RCV004317437]	uncertain significance	13	87676973	87676973	Human		name
401909163	CV2803853	single nucleotide variant	NM_001384609.1(SLITRK5):c.2820C>G (p.Asn940Lys)	SLITRK5-related disorder [RCV003397786]\|not specified [RCV004867869]	uncertain significance	13	87678208	87678208	Human		name , trait , alternate_id
404993857	CV2851075	single nucleotide variant	NM_001384609.1(SLITRK5):c.2527G>T (p.Asp843Tyr)	not provided [RCV003491523]	uncertain significance	13	87677915	87677915	Human		name
405286718	CV3205466	single nucleotide variant	NM_001384609.1(SLITRK5):c.1829T>A (p.Leu610Gln)	SLITRK5-related disorder [RCV003959630]	benign	13	87677217	87677217	Human		name , trait , alternate_id
405266450	CV3211792	single nucleotide variant	NM_001384609.1(SLITRK5):c.2209G>T (p.Ala737Ser)	SLITRK5-related disorder [RCV003947083]	likely benign	13	87677597	87677597	Human		name , trait , alternate_id
405785687	CV3333165	single nucleotide variant	NM_001384609.1(SLITRK5):c.1214A>G (p.Gln405Arg)	not specified [RCV004459495]	uncertain significance	13	87676602	87676602	Human		name
405785692	CV3333166	single nucleotide variant	NM_001384609.1(SLITRK5):c.1340T>A (p.Met447Lys)	not specified [RCV004459496]	uncertain significance	13	87676728	87676728	Human		name
405785697	CV3333167	single nucleotide variant	NM_001384609.1(SLITRK5):c.1508C>G (p.Pro503Arg)	not specified [RCV004459497]	uncertain significance	13	87676896	87676896	Human		name
405785702	CV3333168	single nucleotide variant	NM_001384609.1(SLITRK5):c.1814C>T (p.Ser605Phe)	not specified [RCV004459498]	uncertain significance	13	87677202	87677202	Human		name
405785708	CV3333169	single nucleotide variant	NM_001384609.1(SLITRK5):c.1853T>C (p.Val618Ala)	not specified [RCV004459499]	uncertain significance	13	87677241	87677241	Human		name
405785714	CV3333170	single nucleotide variant	NM_001384609.1(SLITRK5):c.1909G>T (p.Val637Leu)	not specified [RCV004459500]	uncertain significance	13	87677297	87677297	Human		name
405785719	CV3333171	single nucleotide variant	NM_001384609.1(SLITRK5):c.1942G>A (p.Ala648Thr)	not specified [RCV004459501]	uncertain significance	13	87677330	87677330	Human		name
405785729	CV3333173	single nucleotide variant	NM_001384609.1(SLITRK5):c.2093A>G (p.Asp698Gly)	not specified [RCV004459503]	uncertain significance	13	87677481	87677481	Human		name
405785733	CV3333174	single nucleotide variant	NM_001384609.1(SLITRK5):c.2097C>G (p.His699Gln)	not specified [RCV004459504]	uncertain significance	13	87677485	87677485	Human		name
405785738	CV3333175	single nucleotide variant	NM_001384609.1(SLITRK5):c.2108A>G (p.Asn703Ser)	not specified [RCV004459505]	uncertain significance	13	87677496	87677496	Human		name
405785744	CV3333176	single nucleotide variant	NM_001384609.1(SLITRK5):c.2191G>A (p.Val731Met)	not specified [RCV004459506]	uncertain significance	13	87677579	87677579	Human		name
405785749	CV3333177	single nucleotide variant	NM_001384609.1(SLITRK5):c.2341G>C (p.Glu781Gln)	not specified [RCV004459507]	uncertain significance	13	87677729	87677729	Human		name
405785755	CV3333178	single nucleotide variant	NM_001384609.1(SLITRK5):c.2461G>A (p.Glu821Lys)	not specified [RCV004459508]	uncertain significance	13	87677849	87677849	Human		name
405785759	CV3333179	single nucleotide variant	NM_001384609.1(SLITRK5):c.2517G>C (p.Glu839Asp)	not specified [RCV004459509]	uncertain significance	13	87677905	87677905	Human		name
405785764	CV3333180	single nucleotide variant	NM_001384609.1(SLITRK5):c.2540C>T (p.Pro847Leu)	not specified [RCV004459510]	uncertain significance	13	87677928	87677928	Human		name
405785771	CV3333181	single nucleotide variant	NM_001384609.1(SLITRK5):c.2657C>T (p.Ala886Val)	not specified [RCV004459511]	uncertain significance	13	87678045	87678045	Human		name
405785778	CV3333183	single nucleotide variant	NM_001384609.1(SLITRK5):c.2784C>G (p.Asn928Lys)	not specified [RCV004459513]	uncertain significance	13	87678172	87678172	Human		name
407452232	CV3477501	single nucleotide variant	NM_001384609.1(SLITRK5):c.1433A>G (p.Tyr478Cys)	not specified [RCV004683943]	uncertain significance	13	87676821	87676821	Human		name
407494101	CV3477502	single nucleotide variant	NM_001384609.1(SLITRK5):c.1751G>C (p.Gly584Ala)	not specified [RCV004667547]	uncertain significance	13	87677139	87677139	Human		name
407452234	CV3477503	single nucleotide variant	NM_001384609.1(SLITRK5):c.2378A>C (p.Gln793Pro)	not specified [RCV004683944]	uncertain significance	13	87677766	87677766	Human		name
407494106	CV3477504	single nucleotide variant	NM_001384609.1(SLITRK5):c.2413C>T (p.Pro805Ser)	not specified [RCV004667548]	uncertain significance	13	87677801	87677801	Human		name
407452236	CV3477505	single nucleotide variant	NM_001384609.1(SLITRK5):c.1187G>A (p.Arg396Gln)	not specified [RCV004683945]	uncertain significance	13	87676575	87676575	Human		name
407452240	CV3477508	single nucleotide variant	NM_001384609.1(SLITRK5):c.2743G>A (p.Val915Met)	not specified [RCV004683947]	uncertain significance	13	87678131	87678131	Human		name
407494116	CV3477510	single nucleotide variant	NM_001384609.1(SLITRK5):c.1659G>C (p.Lys553Asn)	not specified [RCV004667551]	uncertain significance	13	87677047	87677047	Human		name
407452242	CV3477511	single nucleotide variant	NM_001384609.1(SLITRK5):c.2597C>T (p.Ser866Phe)	not specified [RCV004683948]	uncertain significance	13	87677985	87677985	Human		name
407494120	CV3477512	single nucleotide variant	NM_001384609.1(SLITRK5):c.2124C>A (p.Ser708Arg)	not specified [RCV004667552]	uncertain significance	13	87677512	87677512	Human		name
407494125	CV3477514	single nucleotide variant	NM_001384609.1(SLITRK5):c.2722G>T (p.Asp908Tyr)	not specified [RCV004667553]	uncertain significance	13	87678110	87678110	Human		name
407494128	CV3477515	single nucleotide variant	NM_001384609.1(SLITRK5):c.1649A>G (p.Asp550Gly)	not specified [RCV004667554]	uncertain significance	13	87677037	87677037	Human		name
597778036	CV3603402	single nucleotide variant	NM_001384609.1(SLITRK5):c.1418G>T (p.Ser473Ile)	not specified [RCV004873180]	uncertain significance	13	87676806	87676806	Human		name
597726319	CV3603405	single nucleotide variant	NM_001384609.1(SLITRK5):c.2692C>T (p.Pro898Ser)	not specified [RCV004862549]	uncertain significance	13	87678080	87678080	Human		name
597726327	CV3603406	single nucleotide variant	NM_001384609.1(SLITRK5):c.1886A>G (p.Gln629Arg)	not specified [RCV004862550]	uncertain significance	13	87677274	87677274	Human		name
597778040	CV3603407	single nucleotide variant	NM_001384609.1(SLITRK5):c.1199G>T (p.Ser400Ile)	not specified [RCV004873181]	uncertain significance	13	87676587	87676587	Human		name
597726335	CV3603408	single nucleotide variant	NM_001384609.1(SLITRK5):c.2591A>G (p.His864Arg)	not specified [RCV004862551]	uncertain significance	13	87677979	87677979	Human		name
597726341	CV3603409	single nucleotide variant	NM_001384609.1(SLITRK5):c.2056G>C (p.Val686Leu)	not specified [RCV004862552]	uncertain significance	13	87677444	87677444	Human		name
597726349	CV3603411	single nucleotide variant	NM_001384609.1(SLITRK5):c.1727T>A (p.Leu576Gln)	not specified [RCV004862553]	uncertain significance	13	87677115	87677115	Human		name
597778048	CV3603412	single nucleotide variant	NM_001384609.1(SLITRK5):c.2209G>C (p.Ala737Pro)	not specified [RCV004873183]	uncertain significance	13	87677597	87677597	Human		name
597778052	CV3603413	single nucleotide variant	NM_001384609.1(SLITRK5):c.1432T>C (p.Tyr478His)	not specified [RCV004873184]	uncertain significance	13	87676820	87676820	Human		name
597726355	CV3603414	single nucleotide variant	NM_001384609.1(SLITRK5):c.1274G>T (p.Arg425Leu)	not specified [RCV004862554]	uncertain significance	13	87676662	87676662	Human		name
597778055	CV3603415	single nucleotide variant	NM_001384609.1(SLITRK5):c.2644T>C (p.Cys882Arg)	not specified [RCV004873185]	uncertain significance	13	87678032	87678032	Human		name
12858868	CV389157	single nucleotide variant	NM_001384609.1(SLITRK5):c.2515G>C (p.Glu839Gln)	Abnormal brain morphology [RCV000454171]	likely pathogenic	13	87677903	87677903	Human	1	name
598270290	CV3918547	single nucleotide variant	NM_001384609.1(SLITRK5):c.2468G>C (p.Arg823Pro)	not specified [RCV005282125]	uncertain significance	13	87677856	87677856	Human		name
598270295	CV3918548	single nucleotide variant	NM_001384609.1(SLITRK5):c.2644T>A (p.Cys882Ser)	not specified [RCV005282126]	uncertain significance	13	87678032	87678032	Human		name
598270300	CV3918549	single nucleotide variant	NM_001384609.1(SLITRK5):c.1475T>C (p.Leu492Pro)	not specified [RCV005282127]	uncertain significance	13	87676863	87676863	Human		name
598270306	CV3918550	single nucleotide variant	NM_001384609.1(SLITRK5):c.1480C>T (p.Arg494Cys)	not specified [RCV005282128]	uncertain significance	13	87676868	87676868	Human		name
598270317	CV3918552	single nucleotide variant	NM_001384609.1(SLITRK5):c.2489G>T (p.Ser830Ile)	not specified [RCV005282130]	uncertain significance	13	87677877	87677877	Human		name
598270329	CV3918555	single nucleotide variant	NM_001384609.1(SLITRK5):c.1577C>T (p.Ser526Phe)	not specified [RCV005282132]	uncertain significance	13	87676965	87676965	Human		name
598270334	CV3918556	single nucleotide variant	NM_001384609.1(SLITRK5):c.1459T>C (p.Phe487Leu)	not specified [RCV005282133]	uncertain significance	13	87676847	87676847	Human		name

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