Dpysl4 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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68 records found for search term Dpysl4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329354492	CV2448284	single nucleotide variant	NM_006426.3(DPYSL4):c.32G>A (p.Arg11Gln)	not specified [RCV004263483]	uncertain significance	10	132187095	132187095	Human		name
405713313	CV3248046	single nucleotide variant	NM_006426.3(DPYSL4):c.38C>T (p.Thr13Met)	not specified [RCV004377001]	uncertain significance	10	132187101	132187101	Human		name
405713319	CV3248047	single nucleotide variant	NM_006426.3(DPYSL4):c.46C>T (p.Arg16Cys)	not specified [RCV004377002]	uncertain significance	10	132190753	132190753	Human		name
598187242	CV3960938	single nucleotide variant	NM_006426.3(DPYSL4):c.969C>T (p.Ser323=)	not specified [RCV005334180]	likely benign	10	132200842	132200842	Human		name
156049794	CV2319332	single nucleotide variant	NM_006426.3(DPYSL4):c.262G>A (p.Asp88Asn)	not specified [RCV004180157]	uncertain significance	10	132192791	132192791	Human		name
155966764	CV2396109	single nucleotide variant	NM_006426.3(DPYSL4):c.151G>A (p.Val51Ile)	not specified [RCV004237641]	uncertain significance	10	132192680	132192680	Human		name
329390844	CV2437339	single nucleotide variant	NM_006426.3(DPYSL4):c.261C>A (p.Asp87Glu)	not specified [RCV004256214]	uncertain significance	10	132192790	132192790	Human		name
401773075	CV2709108	single nucleotide variant	NM_006426.3(DPYSL4):c.133A>G (p.Ile45Val)	not specified [RCV004314439]	uncertain significance	10	132192662	132192662	Human		name
401878647	CV2754731	single nucleotide variant	NM_006426.3(DPYSL4):c.241C>A (p.Leu81Met)	not specified [RCV004339399]	uncertain significance	10	132192770	132192770	Human		name
155939665	CV2225637	single nucleotide variant	NM_006426.3(DPYSL4):c.805C>T (p.Arg269Cys)	not specified [RCV004102793]	uncertain significance	10	132198965	132198965	Human		name
156051119	CV2237920	single nucleotide variant	NM_006426.3(DPYSL4):c.502A>G (p.Met168Val)	not specified [RCV004109145]	uncertain significance	10	132196884	132196884	Human		name
156363756	CV2330034	single nucleotide variant	NM_006426.3(DPYSL4):c.331G>A (p.Asp111Asn)	not specified [RCV004185526]	uncertain significance	10	132194862	132194862	Human		name
156073473	CV2331586	single nucleotide variant	NM_006426.3(DPYSL4):c.308T>C (p.Met103Thr)	not specified [RCV004184226]	uncertain significance	10	132192837	132192837	Human		name
155989863	CV2352286	single nucleotide variant	NM_006426.3(DPYSL4):c.646G>A (p.Gly216Ser)	not specified [RCV004200761]	uncertain significance	10	132198439	132198439	Human		name
155986915	CV2354817	single nucleotide variant	NM_006426.3(DPYSL4):c.938C>T (p.Thr313Met)	not specified [RCV004198344]	uncertain significance	10	132200482	132200482	Human		name
156096299	CV2399065	single nucleotide variant	NM_006426.3(DPYSL4):c.517C>T (p.Arg173Trp)	not specified [RCV004245361]	uncertain significance	10	132196899	132196899	Human		name
401758785	CV2694277	single nucleotide variant	NM_006426.3(DPYSL4):c.856G>A (p.Asp286Asn)	not specified [RCV004304477]	uncertain significance	10	132200400	132200400	Human		name
401765149	CV2712504	single nucleotide variant	NM_006426.3(DPYSL4):c.925C>T (p.Pro309Ser)	not specified [RCV004307850]	uncertain significance	10	132200469	132200469	Human		name
401874745	CV2756032	single nucleotide variant	NM_006426.3(DPYSL4):c.384C>G (p.Asp128Glu)	not specified [RCV004338158]	uncertain significance	10	132194915	132194915	Human		name
405713328	CV3248048	single nucleotide variant	NM_006426.3(DPYSL4):c.691G>A (p.Val231Met)	not specified [RCV004377003]	uncertain significance	10	132198851	132198851	Human		name
407488839	CV3434656	single nucleotide variant	NM_006426.3(DPYSL4):c.605G>C (p.Gly202Ala)	not specified [RCV004619807]	uncertain significance	10	132197085	132197085	Human		name
407488845	CV3434657	single nucleotide variant	NM_006426.3(DPYSL4):c.539A>G (p.Gln180Arg)	not specified [RCV004619808]	uncertain significance	10	132196921	132196921	Human		name
407488850	CV3434658	single nucleotide variant	NM_006426.3(DPYSL4):c.925C>G (p.Pro309Ala)	not specified [RCV004619809]	uncertain significance	10	132200469	132200469	Human		name
407488868	CV3434661	single nucleotide variant	NM_006426.3(DPYSL4):c.998A>G (p.His333Arg)	not specified [RCV004619812]	uncertain significance	10	132200871	132200871	Human		name
597680998	CV3663744	single nucleotide variant	NM_006426.3(DPYSL4):c.553T>C (p.Phe185Leu)	not specified [RCV004914289]	uncertain significance	10	132197033	132197033	Human		name
597681006	CV3663745	single nucleotide variant	NM_006426.3(DPYSL4):c.370C>T (p.Arg124Trp)	not specified [RCV004914290]	uncertain significance	10	132194901	132194901	Human		name
597681015	CV3663746	single nucleotide variant	NM_006426.3(DPYSL4):c.767T>C (p.Met256Thr)	not specified [RCV004914291]	uncertain significance	10	132198927	132198927	Human		name
597681032	CV3663748	single nucleotide variant	NM_006426.3(DPYSL4):c.386G>C (p.Ser129Thr)	not specified [RCV004914293]	uncertain significance	10	132194917	132194917	Human		name
597734694	CV3663749	single nucleotide variant	NM_006426.3(DPYSL4):c.380C>G (p.Ala127Gly)	not specified [RCV004920318]	uncertain significance	10	132194911	132194911	Human		name
597681050	CV3663751	single nucleotide variant	NM_006426.3(DPYSL4):c.623A>G (p.Glu208Gly)	not specified [RCV004914295]	uncertain significance	10	132198416	132198416	Human		name
597681066	CV3663753	single nucleotide variant	NM_006426.3(DPYSL4):c.625C>G (p.Gln209Glu)	not specified [RCV004914297]	uncertain significance	10	132198418	132198418	Human		name
598187235	CV3960937	single nucleotide variant	NM_006426.3(DPYSL4):c.806G>A (p.Arg269His)	not specified [RCV005334179]	uncertain significance	10	132198966	132198966	Human		name
598187278	CV3960943	single nucleotide variant	NM_006426.3(DPYSL4):c.943G>C (p.Asp315His)	not specified [RCV005334185]	uncertain significance	10	132200487	132200487	Human		name
598187286	CV3960944	single nucleotide variant	NM_006426.3(DPYSL4):c.467T>G (p.Val156Gly)	not specified [RCV005334186]	uncertain significance	10	132194998	132194998	Human		name
598187293	CV3960945	single nucleotide variant	NM_006426.3(DPYSL4):c.543G>A (p.Met181Ile)	not specified [RCV005334187]	uncertain significance	10	132197023	132197023	Human		name
598187301	CV3960946	single nucleotide variant	NM_006426.3(DPYSL4):c.692T>C (p.Val231Ala)	not specified [RCV005334188]	uncertain significance	10	132198852	132198852	Human		name
598187308	CV3960947	single nucleotide variant	NM_006426.3(DPYSL4):c.859G>A (p.Gly287Ser)	not specified [RCV005334189]	uncertain significance	10	132200403	132200403	Human		name
156375510	CV2210207	single nucleotide variant	NM_006426.3(DPYSL4):c.1388C>T (p.Pro463Leu)	not specified [RCV004087588]	uncertain significance	10	132202752	132202752	Human		name
155927639	CV2230819	single nucleotide variant	NM_006426.3(DPYSL4):c.1255A>T (p.Ile419Phe)	not specified [RCV004092033]	uncertain significance	10	132202090	132202090	Human		name
156018956	CV2301704	single nucleotide variant	NM_006426.3(DPYSL4):c.1339A>T (p.Ile447Leu)	not specified [RCV004156527]	uncertain significance	10	132202703	132202703	Human		name
156264674	CV2329461	single nucleotide variant	NM_006426.3(DPYSL4):c.1478G>A (p.Gly493Asp)	not specified [RCV004187464]	uncertain significance	10	132203778	132203778	Human		name
156243846	CV2347106	single nucleotide variant	NM_006426.3(DPYSL4):c.1562C>G (p.Ser521Cys)	not specified [RCV004204588]	uncertain significance	10	132203862	132203862	Human		name
156193832	CV2398112	single nucleotide variant	NM_006426.3(DPYSL4):c.1180T>G (p.Phe394Val)	not specified [RCV004241696]	uncertain significance	10	132202015	132202015	Human		name
329374501	CV2430920	single nucleotide variant	NM_006426.3(DPYSL4):c.1319G>A (p.Arg440Gln)	not specified [RCV004248521]	uncertain significance	10	132202683	132202683	Human		name
329388373	CV2437352	single nucleotide variant	NM_006426.3(DPYSL4):c.1244A>G (p.Lys415Arg)	not specified [RCV004256224]	likely benign	10	132202079	132202079	Human		name
401735421	CV2672648	single nucleotide variant	NM_006426.3(DPYSL4):c.1277A>G (p.Asn426Ser)	not specified [RCV004287670]	uncertain significance	10	132202112	132202112	Human		name
401738301	CV2676238	single nucleotide variant	NM_006426.3(DPYSL4):c.1466C>T (p.Ala489Val)	not specified [RCV004286282]	uncertain significance	10	132203766	132203766	Human		name
401880388	CV2763023	single nucleotide variant	NM_006426.3(DPYSL4):c.1507G>A (p.Val503Ile)	not specified [RCV004336084]	uncertain significance	10	132203807	132203807	Human		name
401887700	CV2770100	single nucleotide variant	NM_006426.3(DPYSL4):c.1369G>A (p.Gly457Arg)	not specified [RCV004356009]	uncertain significance	10	132202733	132202733	Human		name
405713259	CV3248038	single nucleotide variant	NM_006426.3(DPYSL4):c.1004C>T (p.Thr335Ile)	not specified [RCV004376993]	uncertain significance	10	132200877	132200877	Human		name
405713265	CV3248039	single nucleotide variant	NM_006426.3(DPYSL4):c.1044C>A (p.Phe348Leu)	not specified [RCV004376994]	uncertain significance	10	132200917	132200917	Human		name
405713273	CV3248040	single nucleotide variant	NM_006426.3(DPYSL4):c.1046C>T (p.Ala349Val)	not specified [RCV004376995]	uncertain significance	10	132200919	132200919	Human		name
405713277	CV3248041	single nucleotide variant	NM_006426.3(DPYSL4):c.1318C>T (p.Arg440Trp)	not specified [RCV004376996]	uncertain significance	10	132202682	132202682	Human		name
405713861	CV3248042	single nucleotide variant	NM_006426.3(DPYSL4):c.1325C>T (p.Ala442Val)	not specified [RCV004376997]	uncertain significance	10	132202689	132202689	Human		name
405713295	CV3248043	single nucleotide variant	NM_006426.3(DPYSL4):c.1486C>T (p.Arg496Cys)	not specified [RCV004376998]	uncertain significance	10	132203786	132203786	Human		name
405713300	CV3248044	single nucleotide variant	NM_006426.3(DPYSL4):c.1487G>A (p.Arg496His)	not specified [RCV004376999]	uncertain significance	10	132203787	132203787	Human		name
405713307	CV3248045	single nucleotide variant	NM_006426.3(DPYSL4):c.1501G>A (p.Gly501Arg)	not specified [RCV004377000]	uncertain significance	10	132203801	132203801	Human		name
407488822	CV3434653	single nucleotide variant	NM_006426.3(DPYSL4):c.1477G>A (p.Gly493Ser)	not specified [RCV004619804]	uncertain significance	10	132203777	132203777	Human		name
407488827	CV3434654	single nucleotide variant	NM_006426.3(DPYSL4):c.1333G>A (p.Val445Met)	not specified [RCV004619805]	uncertain significance	10	132202697	132202697	Human		name
407488833	CV3434655	single nucleotide variant	NM_006426.3(DPYSL4):c.1567C>T (p.Pro523Ser)	not specified [RCV004619806]	uncertain significance	10	132203867	132203867	Human		name
407488856	CV3434659	single nucleotide variant	NM_006426.3(DPYSL4):c.1057G>A (p.Glu353Lys)	not specified [RCV004619810]	uncertain significance	10	132200930	132200930	Human		name
597681024	CV3663747	single nucleotide variant	NM_006426.3(DPYSL4):c.1169A>G (p.Lys390Arg)	not specified [RCV004914292]	uncertain significance	10	132202004	132202004	Human		name
597681041	CV3663750	single nucleotide variant	NM_006426.3(DPYSL4):c.1048C>A (p.Leu350Met)	not specified [RCV004914294]	uncertain significance	10	132200921	132200921	Human		name
597681059	CV3663752	single nucleotide variant	NM_006426.3(DPYSL4):c.1363G>C (p.Glu455Gln)	not specified [RCV004914296]	uncertain significance	10	132202727	132202727	Human		name
598187249	CV3960939	single nucleotide variant	NM_006426.3(DPYSL4):c.1550C>T (p.Pro517Leu)	not specified [RCV005334181]	uncertain significance	10	132203850	132203850	Human		name
598187257	CV3960940	single nucleotide variant	NM_006426.3(DPYSL4):c.1601T>G (p.Leu534Arg)	not specified [RCV005334182]	uncertain significance	10	132203901	132203901	Human		name
598187265	CV3960941	single nucleotide variant	NM_006426.3(DPYSL4):c.1577T>C (p.Ile526Thr)	not specified [RCV005334183]	uncertain significance	10	132203877	132203877	Human		name
598187271	CV3960942	single nucleotide variant	NM_006426.3(DPYSL4):c.1546G>A (p.Ala516Thr)	not specified [RCV005334184]	likely benign	10	132203846	132203846	Human		name

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