Dusp16 Variant Search Result - Rat Genome Database

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59 records found for search term Dusp16

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15190081	CV730849	single nucleotide variant	NM_030640.3(DUSP16):c.229-7A>C	not provided [RCV000888003]	benign	12	12520007	12520007	Human		name
156082589	CV2368929	single nucleotide variant	NM_030640.3(DUSP16):c.7C>A (p.His3Asn)	not specified [RCV004207882]	uncertain significance	12	12521092	12521092	Human		name
598267110	CV3957517	single nucleotide variant	NM_030640.3(DUSP16):c.4G>A (p.Ala2Thr)	not specified [RCV005326815]	uncertain significance	12	12521095	12521095	Human		name
405735303	CV3241240	single nucleotide variant	NM_030640.3(DUSP16):c.27A>C (p.Gln9His)	not specified [RCV004379674]	uncertain significance	12	12521072	12521072	Human		name
156076471	CV2248338	single nucleotide variant	NM_030640.3(DUSP16):c.71A>G (p.Glu24Gly)	not specified [RCV004119494]	uncertain significance	12	12521028	12521028	Human		name
401905974	CV2810217	single nucleotide variant	NM_030640.3(DUSP16):c.768C>T (p.Ile256=)	not provided [RCV003396243]	likely benign	12	12480270	12480270	Human		name
405735292	CV3241241	single nucleotide variant	NM_030640.3(DUSP16):c.41G>A (p.Arg14Lys)	not specified [RCV004379675]	uncertain significance	12	12521058	12521058	Human		name
15131747	CV738536	single nucleotide variant	NM_030640.3(DUSP16):c.663G>T (p.Pro221=)	not provided [RCV000897830]	likely benign	12	12487056	12487056	Human		name
155918908	CV2279314	single nucleotide variant	NM_030640.3(DUSP16):c.218C>T (p.Ala73Val)	not specified [RCV004139830]	uncertain significance	12	12520881	12520881	Human		name
401905971	CV2810215	single nucleotide variant	NM_030640.3(DUSP16):c.1158C>T (p.Ser386=)	not provided [RCV003396241]	likely benign	12	12477673	12477673	Human		name
401905972	CV2810216	single nucleotide variant	NM_030640.3(DUSP16):c.1080G>A (p.Val360=)	not provided [RCV003396242]	likely benign	12	12477751	12477751	Human		name
407490301	CV3431100	single nucleotide variant	NM_030640.3(DUSP16):c.124A>G (p.Ile42Val)	not specified [RCV004620144]	uncertain significance	12	12520975	12520975	Human		name
597735227	CV3674043	single nucleotide variant	NM_030640.3(DUSP16):c.272G>T (p.Ser91Ile)	not specified [RCV004920430]	uncertain significance	12	12519957	12519957	Human		name
598267099	CV3957514	single nucleotide variant	NM_030640.3(DUSP16):c.183C>G (p.Asp61Glu)	not specified [RCV005326812]	uncertain significance	12	12520916	12520916	Human		name
156253767	CV2193137	single nucleotide variant	NM_030640.3(DUSP16):c.916G>C (p.Gly306Arg)	not specified [RCV004071137]	uncertain significance	12	12477915	12477915	Human		name
156227575	CV2222842	single nucleotide variant	NM_030640.3(DUSP16):c.925A>G (p.Ser309Gly)	not specified [RCV004101668]	uncertain significance	12	12477906	12477906	Human		name
156204283	CV2234708	single nucleotide variant	NM_030640.3(DUSP16):c.421A>G (p.Thr141Ala)	not specified [RCV004102654]	uncertain significance	12	12500629	12500629	Human		name
156252989	CV2284007	single nucleotide variant	NM_030640.3(DUSP16):c.329A>G (p.Lys110Arg)	not specified [RCV004144621]	uncertain significance	12	12519900	12519900	Human		name
156039611	CV2390348	single nucleotide variant	NM_030640.3(DUSP16):c.908G>A (p.Gly303Glu)	not specified [RCV004240710]	uncertain significance	12	12477923	12477923	Human		name
329383961	CV2434928	single nucleotide variant	NM_030640.3(DUSP16):c.494A>G (p.Asn165Ser)	not specified [RCV004250798]	uncertain significance	12	12500556	12500556	Human		name
329370711	CV2461838	single nucleotide variant	NM_030640.3(DUSP16):c.623G>A (p.Arg208His)	not specified [RCV004271754]	uncertain significance	12	12487096	12487096	Human		name
401890023	CV2763595	single nucleotide variant	NM_030640.3(DUSP16):c.890A>T (p.Lys297Met)	not specified [RCV004343104]	uncertain significance	12	12477941	12477941	Human		name
401864602	CV2781882	single nucleotide variant	NM_030640.3(DUSP16):c.607G>A (p.Glu203Lys)	not specified [RCV004356824]	uncertain significance	12	12487112	12487112	Human		name
405735284	CV3241242	single nucleotide variant	NM_030640.3(DUSP16):c.613C>T (p.His205Tyr)	not specified [RCV004379676]	uncertain significance	12	12487106	12487106	Human		name
405735276	CV3241243	single nucleotide variant	NM_030640.3(DUSP16):c.980C>T (p.Ser327Leu)	not specified [RCV004379677]	uncertain significance	12	12477851	12477851	Human		name
405735270	CV3241244	single nucleotide variant	NM_030640.3(DUSP16):c.988G>A (p.Gly330Arg)	not specified [RCV004379678]	uncertain significance	12	12477843	12477843	Human		name
407490292	CV3431097	single nucleotide variant	NM_030640.3(DUSP16):c.805G>A (p.Glu269Lys)	not specified [RCV004620141]	uncertain significance	12	12480233	12480233	Human		name
407490295	CV3431098	single nucleotide variant	NM_030640.3(DUSP16):c.775A>G (p.Ile259Val)	not specified [RCV004620142]	uncertain significance	12	12480263	12480263	Human		name
597802433	CV3674044	single nucleotide variant	NM_030640.3(DUSP16):c.389G>A (p.Arg130His)	not specified [RCV004906681]	uncertain significance	12	12500661	12500661	Human		name
597802442	CV3674048	single nucleotide variant	NM_030640.3(DUSP16):c.425T>C (p.Leu142Pro)	not specified [RCV004906685]	uncertain significance	12	12500625	12500625	Human		name
597802444	CV3674049	single nucleotide variant	NM_030640.3(DUSP16):c.443C>T (p.Ser148Phe)	not specified [RCV004906686]	uncertain significance	12	12500607	12500607	Human		name
156242424	CV2210684	single nucleotide variant	NM_030640.3(DUSP16):c.1967C>T (p.Ser656Leu)	not specified [RCV004083825]	uncertain significance	12	12476864	12476864	Human		name
156336905	CV2228609	single nucleotide variant	NM_030640.3(DUSP16):c.1552C>T (p.Leu518Phe)	not specified [RCV004092837]	uncertain significance	12	12477279	12477279	Human		name
155922801	CV2251775	single nucleotide variant	NM_030640.3(DUSP16):c.1312G>A (p.Gly438Arg)	not specified [RCV004119767]	uncertain significance	12	12477519	12477519	Human		name
156162146	CV2323511	single nucleotide variant	NM_030640.3(DUSP16):c.1042G>A (p.Glu348Lys)	not specified [RCV004165717]	uncertain significance	12	12477789	12477789	Human		name
155990465	CV2352464	single nucleotide variant	NM_030640.3(DUSP16):c.1873C>T (p.Arg625Cys)	not specified [RCV004202972]	uncertain significance	12	12476958	12476958	Human		name
156264566	CV2364334	single nucleotide variant	NM_030640.3(DUSP16):c.1457C>T (p.Ser486Leu)	not specified [RCV004223554]	uncertain significance	12	12477374	12477374	Human		name
156020076	CV2367053	single nucleotide variant	NM_030640.3(DUSP16):c.1715T>C (p.Ile572Thr)	not specified [RCV004215501]	uncertain significance	12	12477116	12477116	Human		name
329401481	CV2460944	single nucleotide variant	NM_030640.3(DUSP16):c.1792C>T (p.Arg598Cys)	not specified [RCV004265105]	uncertain significance	12	12477039	12477039	Human		name
401763682	CV2725252	single nucleotide variant	NM_030640.3(DUSP16):c.1700A>G (p.Tyr567Cys)	not specified [RCV004319923]	uncertain significance	12	12477131	12477131	Human		name
401862655	CV2762306	single nucleotide variant	NM_030640.3(DUSP16):c.1780G>A (p.Val594Ile)	not specified [RCV004335422]	uncertain significance	12	12477051	12477051	Human		name
401872218	CV2779593	single nucleotide variant	NM_030640.3(DUSP16):c.1586C>T (p.Thr529Met)	not specified [RCV004351303]	uncertain significance	12	12477245	12477245	Human		name
405734795	CV3241234	single nucleotide variant	NM_030640.3(DUSP16):c.1072G>A (p.Ala358Thr)	not specified [RCV004379668]	uncertain significance	12	12477759	12477759	Human		name
405734803	CV3241235	single nucleotide variant	NM_030640.3(DUSP16):c.1075A>G (p.Ser359Gly)	not specified [RCV004379669]	uncertain significance	12	12477756	12477756	Human		name
405734811	CV3241236	single nucleotide variant	NM_030640.3(DUSP16):c.1124C>T (p.Pro375Leu)	not specified [RCV004379670]	uncertain significance	12	12477707	12477707	Human		name
405734819	CV3241237	single nucleotide variant	NM_030640.3(DUSP16):c.1355C>G (p.Ser452Trp)	not specified [RCV004379671]	uncertain significance	12	12477476	12477476	Human		name
405734829	CV3241238	single nucleotide variant	NM_030640.3(DUSP16):c.1643C>T (p.Thr548Ile)	not specified [RCV004379672]	uncertain significance	12	12477188	12477188	Human		name
405734837	CV3241239	single nucleotide variant	NM_030640.3(DUSP16):c.1898G>T (p.Gly633Val)	not specified [RCV004379673]	uncertain significance	12	12476933	12476933	Human		name
407490298	CV3431099	single nucleotide variant	NM_030640.3(DUSP16):c.1904G>T (p.Ser635Ile)	not specified [RCV004620143]	uncertain significance	12	12476927	12476927	Human		name
407490304	CV3431101	single nucleotide variant	NM_030640.3(DUSP16):c.1501T>C (p.Ser501Pro)	not specified [RCV004620145]	uncertain significance	12	12477330	12477330	Human		name
597802429	CV3674040	single nucleotide variant	NM_030640.3(DUSP16):c.1106C>T (p.Ser369Leu)	not specified [RCV004906679]	uncertain significance	12	12477725	12477725	Human		name
597802431	CV3674041	single nucleotide variant	NM_030640.3(DUSP16):c.1832G>A (p.Arg611Gln)	not specified [RCV004906680]	uncertain significance	12	12476999	12476999	Human		name
597802435	CV3674045	single nucleotide variant	NM_030640.3(DUSP16):c.1103C>G (p.Pro368Arg)	not specified [RCV004906682]	uncertain significance	12	12477728	12477728	Human		name
597802438	CV3674046	single nucleotide variant	NM_030640.3(DUSP16):c.1095C>A (p.Ser365Arg)	not specified [RCV004906683]	uncertain significance	12	12477736	12477736	Human		name
597802440	CV3674047	single nucleotide variant	NM_030640.3(DUSP16):c.1477G>A (p.Gly493Ser)	not specified [RCV004906684]	uncertain significance	12	12477354	12477354	Human		name
598267103	CV3957515	single nucleotide variant	NM_030640.3(DUSP16):c.1448G>A (p.Arg483Gln)	not specified [RCV005326813]	uncertain significance	12	12477383	12477383	Human		name
598267107	CV3957516	single nucleotide variant	NM_030640.3(DUSP16):c.1831C>T (p.Arg611Trp)	not specified [RCV005326814]	uncertain significance	12	12477000	12477000	Human		name
598267114	CV3957518	single nucleotide variant	NM_030640.3(DUSP16):c.1558G>A (p.Gly520Ser)	not specified [RCV005326816]	uncertain significance	12	12477273	12477273	Human		name
15176233	CV702204	deletion	NM_030640.3(DUSP16):c.1080_1083del (p.Pro361fs)	not provided [RCV000950778]	benign	12	12477748	12477751	Human		name

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