Dpy19l3 Variant Search Result - Rat Genome Database

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59 records found for search term Dpy19l3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156157620	CV2378776	single nucleotide variant	NM_001172774.2(DPY19L3):c.10A>C (p.Ile4Leu)	not specified [RCV004231227]	uncertain significance	19	32408263	32408263	Human		name
329393324	CV2466844	single nucleotide variant	NM_001172774.2(DPY19L3):c.79A>G (p.Lys27Glu)	not specified [RCV004282620]	uncertain significance	19	32408332	32408332	Human		name
597734648	CV3663686	single nucleotide variant	NM_001172774.2(DPY19L3):c.80A>G (p.Lys27Arg)	not specified [RCV004920308]	uncertain significance	19	32408333	32408333	Human		name
598187072	CV3960908	single nucleotide variant	NM_001172774.2(DPY19L3):c.95T>G (p.Leu32Trp)	not specified [RCV005334150]	uncertain significance	19	32408348	32408348	Human		name
156006749	CV2357809	single nucleotide variant	NM_001172774.2(DPY19L3):c.160G>T (p.Ala54Ser)	not specified [RCV004205096]	uncertain significance	19	32411295	32411295	Human		name
598187088	CV3960911	single nucleotide variant	NM_001172774.2(DPY19L3):c.281A>G (p.Tyr94Cys)	not specified [RCV005334153]	uncertain significance	19	32432759	32432759	Human		name
155994760	CV2249314	single nucleotide variant	NM_001172774.2(DPY19L3):c.838A>G (p.Met280Val)	not specified [RCV004118336]	uncertain significance	19	32439893	32439893	Human		name
156395245	CV2325331	single nucleotide variant	NM_001172774.2(DPY19L3):c.653C>G (p.Pro218Arg)	not specified [RCV004177714]	uncertain significance	19	32439168	32439168	Human		name
155904575	CV2385541	single nucleotide variant	NM_001172774.2(DPY19L3):c.695G>C (p.Arg232Thr)	not specified [RCV004233182]	uncertain significance	19	32439210	32439210	Human		name
156198574	CV2400877	single nucleotide variant	NM_001172774.2(DPY19L3):c.904A>G (p.Ile302Val)	not specified [RCV004242526]	uncertain significance	19	32453193	32453193	Human		name
401736031	CV2703022	single nucleotide variant	NM_001172774.2(DPY19L3):c.518C>G (p.Ala173Gly)	not specified [RCV004321331]	uncertain significance	19	32437261	32437261	Human		name
405713751	CV3247989	single nucleotide variant	NM_001172774.2(DPY19L3):c.322G>A (p.Val108Met)	not specified [RCV004376944]	likely benign	19	32432800	32432800	Human		name
405713738	CV3247991	single nucleotide variant	NM_001172774.2(DPY19L3):c.949A>G (p.Ser317Gly)	not specified [RCV004376946]	uncertain significance	19	32453238	32453238	Human		name
407488710	CV3434632	single nucleotide variant	NM_001172774.2(DPY19L3):c.538C>G (p.Leu180Val)	not specified [RCV004619783]	uncertain significance	19	32437281	32437281	Human		name
597680754	CV3663682	single nucleotide variant	NM_001172774.2(DPY19L3):c.793A>G (p.Met265Val)	not specified [RCV004914258]	uncertain significance	19	32439848	32439848	Human		name
597680761	CV3663684	single nucleotide variant	NM_001172774.2(DPY19L3):c.539T>C (p.Leu180Pro)	not specified [RCV004914259]	uncertain significance	19	32437282	32437282	Human		name
597680767	CV3663685	single nucleotide variant	NM_001172774.2(DPY19L3):c.327A>T (p.Gln109His)	not specified [RCV004914260]	uncertain significance	19	32432805	32432805	Human		name
597680780	CV3663688	single nucleotide variant	NM_001172774.2(DPY19L3):c.838A>C (p.Met280Leu)	not specified [RCV004914262]	uncertain significance	19	32439893	32439893	Human		name
598187047	CV3960904	single nucleotide variant	NM_001172774.2(DPY19L3):c.337G>T (p.Gly113Cys)	not specified [RCV005334146]	uncertain significance	19	32436454	32436454	Human		name
598187078	CV3960909	single nucleotide variant	NM_001172774.2(DPY19L3):c.860C>T (p.Thr287Ile)	not specified [RCV005334151]	uncertain significance	19	32453149	32453149	Human		name
155960869	CV2204382	single nucleotide variant	NM_001172774.2(DPY19L3):c.1342T>C (p.Ser448Pro)	not specified [RCV004079199]	uncertain significance	19	32463385	32463385	Human		name
156372801	CV2204576	single nucleotide variant	NM_001172774.2(DPY19L3):c.1318C>T (p.Leu440Phe)	not specified [RCV004081686]	uncertain significance	19	32458505	32458505	Human		name
156326021	CV2209536	single nucleotide variant	NM_001172774.2(DPY19L3):c.1842A>G (p.Ile614Met)	not specified [RCV004093652]	uncertain significance	19	32480410	32480410	Human		name
156048845	CV2220235	single nucleotide variant	NM_001172774.2(DPY19L3):c.1081A>G (p.Ile361Val)	not specified [RCV004095678]	uncertain significance	19	32455032	32455032	Human		name
156158302	CV2236083	single nucleotide variant	NM_001172774.2(DPY19L3):c.1622C>T (p.Pro541Leu)	not specified [RCV004114238]	uncertain significance	19	32468738	32468738	Human		name
156120603	CV2275934	single nucleotide variant	NM_001172774.2(DPY19L3):c.1985G>A (p.Gly662Asp)	not specified [RCV004139588]	uncertain significance	19	32480553	32480553	Human		name
156036816	CV2283095	single nucleotide variant	NM_001172774.2(DPY19L3):c.1007G>A (p.Ser336Asn)	not specified [RCV004143704]	likely benign	19	32454958	32454958	Human		name
156292255	CV2306195	single nucleotide variant	NM_001172774.2(DPY19L3):c.1879C>G (p.Leu627Val)	not specified [RCV004162939]	uncertain significance	19	32480447	32480447	Human		name
156039815	CV2310744	single nucleotide variant	NM_001172774.2(DPY19L3):c.1016A>G (p.Asn339Ser)	not specified [RCV004157676]	uncertain significance	19	32454967	32454967	Human		name
156271408	CV2315742	single nucleotide variant	NM_001172774.2(DPY19L3):c.1390G>A (p.Ala464Thr)	not specified [RCV004169751]	uncertain significance	19	32463433	32463433	Human		name
155973931	CV2317766	single nucleotide variant	NM_001172774.2(DPY19L3):c.2083G>A (p.Val695Met)	not specified [RCV004175017]	likely benign	19	32482172	32482172	Human		name
156275786	CV2318375	single nucleotide variant	NM_001172774.2(DPY19L3):c.1298T>G (p.Phe433Cys)	not specified [RCV004179535]	uncertain significance	19	32458485	32458485	Human		name
156048723	CV2336466	single nucleotide variant	NM_001172774.2(DPY19L3):c.1724T>C (p.Phe575Ser)	not specified [RCV004194679]	uncertain significance	19	32477548	32477548	Human		name
156189001	CV2356559	single nucleotide variant	NM_001172774.2(DPY19L3):c.1609T>C (p.Tyr537His)	not specified [RCV004201929]	uncertain significance	19	32464779	32464779	Human		name
156084783	CV2366099	single nucleotide variant	NM_001172774.2(DPY19L3):c.1106A>G (p.Lys369Arg)	not specified [RCV004210134]	uncertain significance	19	32458116	32458116	Human		name
156035800	CV2373935	single nucleotide variant	NM_001172774.2(DPY19L3):c.1903G>A (p.Val635Ile)	not specified [RCV004227072]	uncertain significance	19	32480471	32480471	Human		name
155904774	CV2385599	single nucleotide variant	NM_001172774.2(DPY19L3):c.2075C>T (p.Pro692Leu)	not specified [RCV004233235]	uncertain significance	19	32482164	32482164	Human		name
156097782	CV2392729	single nucleotide variant	NM_001172774.2(DPY19L3):c.1612A>G (p.Lys538Glu)	not specified [RCV004247102]	uncertain significance	19	32464782	32464782	Human		name
401752255	CV2682757	single nucleotide variant	NM_001172774.2(DPY19L3):c.2145C>G (p.Asn715Lys)	not specified [RCV004281731]	uncertain significance	19	32482234	32482234	Human		name
401728570	CV2693645	single nucleotide variant	NM_001172774.2(DPY19L3):c.1720G>A (p.Val574Met)	not specified [RCV004297982]	uncertain significance	19	32477544	32477544	Human		name
401878100	CV2786896	single nucleotide variant	NM_001172774.2(DPY19L3):c.1404A>G (p.Ile468Met)	not specified [RCV004366047]	uncertain significance	19	32463447	32463447	Human		name
405713785	CV3247984	single nucleotide variant	NM_001172774.2(DPY19L3):c.1049T>C (p.Met350Thr)	not specified [RCV004376939]	uncertain significance	19	32455000	32455000	Human		name
405713776	CV3247985	single nucleotide variant	NM_001172774.2(DPY19L3):c.1069T>C (p.Phe357Leu)	not specified [RCV004376940]	uncertain significance	19	32455020	32455020	Human		name
405713771	CV3247986	single nucleotide variant	NM_001172774.2(DPY19L3):c.1165G>A (p.Asp389Asn)	not specified [RCV004376941]	uncertain significance	19	32458352	32458352	Human		name
405713763	CV3247987	single nucleotide variant	NM_001172774.2(DPY19L3):c.1946G>A (p.Arg649Gln)	not specified [RCV004376942]	uncertain significance	19	32480514	32480514	Human		name
405713757	CV3247988	single nucleotide variant	NM_001172774.2(DPY19L3):c.2045G>A (p.Arg682His)	not specified [RCV004376943]	uncertain significance	19	32482134	32482134	Human		name
407488699	CV3434630	single nucleotide variant	NM_001172774.2(DPY19L3):c.1994T>G (p.Met665Arg)	not specified [RCV004619781]	uncertain significance	19	32482083	32482083	Human		name
407488720	CV3434633	single nucleotide variant	NM_001172774.2(DPY19L3):c.1283C>T (p.Thr428Ile)	not specified [RCV004619784]	uncertain significance	19	32458470	32458470	Human		name
407488725	CV3434634	single nucleotide variant	NM_001172774.2(DPY19L3):c.1966C>G (p.Leu656Val)	not specified [RCV004619785]	uncertain significance	19	32480534	32480534	Human		name
597680747	CV3663680	single nucleotide variant	NM_001172774.2(DPY19L3):c.1942C>T (p.Arg648Cys)	not specified [RCV004914257]	uncertain significance	19	32480510	32480510	Human		name
597734638	CV3663681	single nucleotide variant	NM_001172774.2(DPY19L3):c.1550C>T (p.Pro517Leu)	not specified [RCV004920306]	uncertain significance	19	32463973	32463973	Human		name
597734643	CV3663683	single nucleotide variant	NM_001172774.2(DPY19L3):c.1747G>T (p.Ala583Ser)	not specified [RCV004920307]	uncertain significance	19	32477571	32477571	Human		name
598187025	CV3960901	single nucleotide variant	NM_001172774.2(DPY19L3):c.1511T>A (p.Ile504Lys)	not specified [RCV005334143]	uncertain significance	19	32463934	32463934	Human		name
598187032	CV3960902	single nucleotide variant	NM_001172774.2(DPY19L3):c.1807A>C (p.Ser603Arg)	not specified [RCV005334144]	uncertain significance	19	32477631	32477631	Human		name
598187038	CV3960903	single nucleotide variant	NM_001172774.2(DPY19L3):c.1735A>C (p.Met579Leu)	not specified [RCV005334145]	uncertain significance	19	32477559	32477559	Human		name
598187057	CV3960906	single nucleotide variant	NM_001172774.2(DPY19L3):c.1300G>A (p.Val434Ile)	not specified [RCV005334148]	uncertain significance	19	32458487	32458487	Human		name
598187065	CV3960907	single nucleotide variant	NM_001172774.2(DPY19L3):c.1808G>A (p.Ser603Asn)	not specified [RCV005334149]	uncertain significance	19	32477632	32477632	Human		name
598187084	CV3960910	single nucleotide variant	NM_001172774.2(DPY19L3):c.1331C>A (p.Thr444Lys)	not specified [RCV005334152]	uncertain significance	19	32463374	32463374	Human		name
598187094	CV3960912	single nucleotide variant	NM_001172774.2(DPY19L3):c.1766C>T (p.Thr589Met)	not specified [RCV005334154]	uncertain significance	19	32477590	32477590	Human		name

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