Snx32 Variant Search Result - Rat Genome Database

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60 records found for search term Snx32

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156039561	CV2261223	single nucleotide variant	NM_152760.3(SNX32):c.223G>A (p.Val75Met)	not specified [RCV004128100]	uncertain significance	11	65850001	65850001	Human		name
405733594	CV3322697	single nucleotide variant	NM_152760.3(SNX32):c.104G>C (p.Ser35Thr)	not specified [RCV004464659]	uncertain significance	11	65849545	65849545	Human		name
405733647	CV3322702	single nucleotide variant	NM_152760.3(SNX32):c.146G>A (p.Cys49Tyr)	not specified [RCV004464664]	uncertain significance	11	65849924	65849924	Human		name
407504063	CV3484848	single nucleotide variant	NM_152760.3(SNX32):c.212A>G (p.His71Arg)	not specified [RCV004670421]	uncertain significance	11	65849990	65849990	Human		name
597755462	CV3607341	single nucleotide variant	NM_152760.3(SNX32):c.185G>A (p.Arg62Gln)	not specified [RCV004868180]	uncertain significance	11	65849963	65849963	Human		name
597741193	CV3607348	single nucleotide variant	NM_152760.3(SNX32):c.263C>A (p.Ala88Asp)	not specified [RCV004864813]	uncertain significance	11	65850160	65850160	Human		name
598172239	CV3911765	single nucleotide variant	NM_152760.3(SNX32):c.154C>T (p.His52Tyr)	not specified [RCV005284994]	uncertain significance	11	65849932	65849932	Human		name
598172245	CV3911766	single nucleotide variant	NM_152760.3(SNX32):c.197A>G (p.Glu66Gly)	not specified [RCV005284995]	uncertain significance	11	65849975	65849975	Human		name
598238499	CV3911768	single nucleotide variant	NM_152760.3(SNX32):c.160G>A (p.Ala54Thr)	not specified [RCV005275843]	uncertain significance	11	65849938	65849938	Human		name
156272098	CV2195288	single nucleotide variant	NM_152760.3(SNX32):c.635C>T (p.Thr212Ile)	not specified [RCV004080215]	uncertain significance	11	65851086	65851086	Human		name
156329512	CV2213850	single nucleotide variant	NM_152760.3(SNX32):c.934C>T (p.Arg312Trp)	not specified [RCV004089903]	uncertain significance	11	65852651	65852651	Human		name
155949928	CV2242798	single nucleotide variant	NM_152760.3(SNX32):c.338G>C (p.Arg113Pro)	not specified [RCV004107394]	uncertain significance	11	65850235	65850235	Human		name
156281069	CV2281816	single nucleotide variant	NM_152760.3(SNX32):c.343G>A (p.Glu115Lys)	not specified [RCV004147945]	uncertain significance	11	65850240	65850240	Human		name
155932081	CV2293880	single nucleotide variant	NM_152760.3(SNX32):c.968C>T (p.Ala323Val)	not specified [RCV004155137]	uncertain significance	11	65852685	65852685	Human		name
156211211	CV2314495	single nucleotide variant	NM_152760.3(SNX32):c.646G>A (p.Glu216Lys)	not specified [RCV004168595]	uncertain significance	11	65851097	65851097	Human		name
156161515	CV2319475	single nucleotide variant	NM_152760.3(SNX32):c.893G>A (p.Arg298His)	not specified [RCV004185053]	uncertain significance	11	65852532	65852532	Human		name
156184025	CV2349884	single nucleotide variant	NM_152760.3(SNX32):c.445C>T (p.Pro149Ser)	not specified [RCV004206305]	uncertain significance	11	65850501	65850501	Human		name
156083403	CV2381879	single nucleotide variant	NM_152760.3(SNX32):c.995G>A (p.Arg332Gln)	not specified [RCV004225823]	uncertain significance	11	65852712	65852712	Human		name
329378460	CV2446950	single nucleotide variant	NM_152760.3(SNX32):c.925C>T (p.Arg309Trp)	not specified [RCV004257794]	uncertain significance	11	65852642	65852642	Human		name
329385382	CV2451331	single nucleotide variant	NM_152760.3(SNX32):c.774C>A (p.Asn258Lys)	not specified [RCV004272021]	uncertain significance	11	65851392	65851392	Human		name
329390673	CV2455360	single nucleotide variant	NM_152760.3(SNX32):c.598C>A (p.Leu200Ile)	not specified [RCV004274860]	uncertain significance	11	65850850	65850850	Human		name
329396098	CV2463252	single nucleotide variant	NM_152760.3(SNX32):c.410T>C (p.Met137Thr)	not specified [RCV004275017]	uncertain significance	11	65850466	65850466	Human		name
401754359	CV2685248	single nucleotide variant	NM_152760.3(SNX32):c.584C>T (p.Thr195Met)	not specified [RCV004289796]	uncertain significance	11	65850836	65850836	Human		name
401743924	CV2696899	single nucleotide variant	NM_152760.3(SNX32):c.458G>A (p.Arg153Gln)	not specified [RCV004292903]	likely benign	11	65850514	65850514	Human		name
401760393	CV2709823	single nucleotide variant	NM_152760.3(SNX32):c.931C>G (p.Leu311Val)	not specified [RCV004320798]	uncertain significance	11	65852648	65852648	Human		name
401734072	CV2713316	single nucleotide variant	NM_152760.3(SNX32):c.400A>G (p.Thr134Ala)	not specified [RCV004316829]	uncertain significance	11	65850456	65850456	Human		name
401742488	CV2715242	single nucleotide variant	NM_152760.3(SNX32):c.821T>C (p.Leu274Pro)	not specified [RCV004324591]	uncertain significance	11	65851675	65851675	Human		name
401862876	CV2755698	single nucleotide variant	NM_152760.3(SNX32):c.967G>A (p.Ala323Thr)	not specified [RCV004342081]	uncertain significance	11	65852684	65852684	Human		name
405733657	CV3322703	single nucleotide variant	NM_152760.3(SNX32):c.415G>A (p.Glu139Lys)	not specified [RCV004464665]	uncertain significance	11	65850471	65850471	Human		name
405733662	CV3322704	single nucleotide variant	NM_152760.3(SNX32):c.509G>A (p.Arg170Gln)	not specified [RCV004464666]	uncertain significance	11	65850761	65850761	Human		name
405733672	CV3322705	single nucleotide variant	NM_152760.3(SNX32):c.539G>A (p.Gly180Glu)	not specified [RCV004464667]	uncertain significance	11	65850791	65850791	Human		name
405733682	CV3322706	single nucleotide variant	NM_152760.3(SNX32):c.587G>A (p.Gly196Asp)	not specified [RCV004464668]	uncertain significance	11	65850839	65850839	Human		name
405733690	CV3322707	single nucleotide variant	NM_152760.3(SNX32):c.590T>C (p.Met197Thr)	not specified [RCV004464669]	uncertain significance	11	65850842	65850842	Human		name
405733698	CV3322708	single nucleotide variant	NM_152760.3(SNX32):c.659G>A (p.Arg220His)	not specified [RCV004464670]	uncertain significance	11	65851110	65851110	Human		name
405733706	CV3322709	single nucleotide variant	NM_152760.3(SNX32):c.755T>G (p.Leu252Arg)	not specified [RCV004464671]	uncertain significance	11	65851373	65851373	Human		name
405733717	CV3322710	single nucleotide variant	NM_152760.3(SNX32):c.832G>A (p.Glu278Lys)	not specified [RCV004464672]	uncertain significance	11	65852471	65852471	Human		name
407525324	CV3484849	single nucleotide variant	NM_152760.3(SNX32):c.980C>T (p.Ala327Val)	not specified [RCV004679146]	uncertain significance	11	65852697	65852697	Human		name
597741175	CV3607343	single nucleotide variant	NM_152760.3(SNX32):c.665G>A (p.Arg222Gln)	not specified [RCV004864809]	uncertain significance	11	65851116	65851116	Human		name
597741180	CV3607344	single nucleotide variant	NM_152760.3(SNX32):c.935G>A (p.Arg312Gln)	not specified [RCV004864810]	uncertain significance	11	65852652	65852652	Human		name
597755470	CV3607345	single nucleotide variant	NM_152760.3(SNX32):c.698G>A (p.Arg233His)	not specified [RCV004868182]	likely benign	11	65851149	65851149	Human		name
597741201	CV3607350	single nucleotide variant	NM_152760.3(SNX32):c.430C>T (p.Arg144Cys)	not specified [RCV004864815]	uncertain significance	11	65850486	65850486	Human		name
597741206	CV3607351	single nucleotide variant	NM_152760.3(SNX32):c.850G>A (p.Asp284Asn)	not specified [RCV004864816]	uncertain significance	11	65852489	65852489	Human		name
597741211	CV3607352	single nucleotide variant	NM_152760.3(SNX32):c.871G>A (p.Asp291Asn)	not specified [RCV004864817]	uncertain significance	11	65852510	65852510	Human		name
597755474	CV3607353	single nucleotide variant	NM_152760.3(SNX32):c.677T>C (p.Leu226Pro)	not specified [RCV004868183]	uncertain significance	11	65851128	65851128	Human		name
598172252	CV3911767	single nucleotide variant	NM_152760.3(SNX32):c.689G>A (p.Arg230His)	not specified [RCV005284996]	uncertain significance	11	65851140	65851140	Human		name
156378212	CV2207659	single nucleotide variant	NM_152760.3(SNX32):c.1009G>A (p.Ala337Thr)	not specified [RCV004090431]	uncertain significance	11	65852726	65852726	Human		name
155928985	CV2224478	single nucleotide variant	NM_152760.3(SNX32):c.1139T>C (p.Leu380Pro)	not specified [RCV004098072]	uncertain significance	11	65852939	65852939	Human		name
156337978	CV2370536	single nucleotide variant	NM_152760.3(SNX32):c.1178G>A (p.Arg393Gln)	not specified [RCV004215872]	uncertain significance	11	65853301	65853301	Human		name
155963261	CV2388370	single nucleotide variant	NM_152760.3(SNX32):c.1112G>T (p.Arg371Leu)	not specified [RCV004234820]	uncertain significance	11	65852912	65852912	Human		name
156164940	CV2389750	single nucleotide variant	NM_152760.3(SNX32):c.1048C>T (p.Arg350Cys)	not specified [RCV004243796]	uncertain significance	11	65852765	65852765	Human		name
401757897	CV2731527	single nucleotide variant	NM_152760.3(SNX32):c.1063G>A (p.Ala355Thr)	not specified [RCV004330876]	uncertain significance	11	65852780	65852780	Human		name
401885825	CV2774557	single nucleotide variant	NM_152760.3(SNX32):c.1177C>T (p.Arg393Trp)	not specified [RCV004350038]	uncertain significance	11	65853300	65853300	Human		name
405733583	CV3322696	single nucleotide variant	NM_152760.3(SNX32):c.1049G>A (p.Arg350His)	not specified [RCV004464658]	uncertain significance	11	65852766	65852766	Human		name
405733602	CV3322698	single nucleotide variant	NM_152760.3(SNX32):c.1091C>A (p.Ser364Tyr)	not specified [RCV004464660]	uncertain significance	11	65852891	65852891	Human		name
405733614	CV3322699	single nucleotide variant	NM_152760.3(SNX32):c.1124T>C (p.Ile375Thr)	not specified [RCV004464661]	uncertain significance	11	65852924	65852924	Human		name
405733622	CV3322700	single nucleotide variant	NM_152760.3(SNX32):c.1130T>C (p.Leu377Pro)	not specified [RCV004464662]	uncertain significance	11	65852930	65852930	Human		name
597755466	CV3607342	single nucleotide variant	NM_152760.3(SNX32):c.1040G>A (p.Arg347His)	not specified [RCV004868181]	uncertain significance	11	65852757	65852757	Human		name
597741184	CV3607346	single nucleotide variant	NM_152760.3(SNX32):c.1112G>A (p.Arg371Gln)	not specified [RCV004864811]	uncertain significance	11	65852912	65852912	Human		name
597741189	CV3607347	single nucleotide variant	NM_152760.3(SNX32):c.1054T>G (p.Ser352Ala)	not specified [RCV004864812]	uncertain significance	11	65852771	65852771	Human		name
597741198	CV3607349	single nucleotide variant	NM_152760.3(SNX32):c.1078A>G (p.Met360Val)	not specified [RCV004864814]	uncertain significance	11	65852878	65852878	Human		name

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