Bcdin3d Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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27 records found for search term Bcdin3d

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329391904	CV2463751	single nucleotide variant	NM_181708.3(BCDIN3D):c.4G>T (p.Ala2Ser)	not specified [RCV004279591]	uncertain significance	12	49843084	49843084	Human		name
11541272	CV248556	single nucleotide variant	NM_181708.3(BCDIN3D):c.23A>G (p.Asp8Gly)	Oromandibular-limb hypogenesis spectrum [RCV000240071]\|not provided [RCV000950779]	benign\|likely benign	12	49843065	49843065	Human	1	name
405707168	CV3301821	single nucleotide variant	NM_181708.3(BCDIN3D):c.77C>G (p.Pro26Arg)	not specified [RCV004426248]	uncertain significance	12	49843011	49843011	Human		name
401775742	CV2710695	single nucleotide variant	NM_181708.3(BCDIN3D):c.224G>C (p.Cys75Ser)	not specified [RCV004319594]	uncertain significance	12	49842864	49842864	Human		name
401865462	CV2757420	single nucleotide variant	NM_181708.3(BCDIN3D):c.244G>A (p.Val82Met)	not specified [RCV004340815]	uncertain significance	12	49839006	49839006	Human		name
405707148	CV3301818	single nucleotide variant	NM_181708.3(BCDIN3D):c.182A>G (p.Glu61Gly)	not specified [RCV004426245]	uncertain significance	12	49842906	49842906	Human		name
405707154	CV3301819	single nucleotide variant	NM_181708.3(BCDIN3D):c.204T>G (p.Ile68Met)	not specified [RCV004426246]	uncertain significance	12	49842884	49842884	Human		name
597736483	CV3639608	single nucleotide variant	NM_181708.3(BCDIN3D):c.236A>G (p.Asp79Gly)	not specified [RCV004889696]	uncertain significance	12	49839014	49839014	Human		name
597736504	CV3639612	single nucleotide variant	NM_181708.3(BCDIN3D):c.205C>G (p.Leu69Val)	not specified [RCV004889700]	uncertain significance	12	49842883	49842883	Human		name
597736515	CV3639615	single nucleotide variant	NM_181708.3(BCDIN3D):c.272T>C (p.Leu91Pro)	not specified [RCV004889702]	uncertain significance	12	49838978	49838978	Human		name
598200023	CV3941923	single nucleotide variant	NM_181708.3(BCDIN3D):c.230C>A (p.Ser77Tyr)	not specified [RCV005313995]	uncertain significance	12	49842858	49842858	Human		name
598273508	CV3941933	single nucleotide variant	NM_181708.3(BCDIN3D):c.203T>G (p.Ile68Ser)	not specified [RCV005303386]	uncertain significance	12	49842885	49842885	Human		name
155978608	CV2215067	single nucleotide variant	NM_181708.3(BCDIN3D):c.833T>C (p.Ile278Thr)	not specified [RCV004084837]	uncertain significance	12	49838417	49838417	Human		name
156331005	CV2224355	single nucleotide variant	NM_181708.3(BCDIN3D):c.314G>A (p.Arg105His)	not specified [RCV004097698]	likely benign	12	49838936	49838936	Human		name
156285537	CV2232837	single nucleotide variant	NM_181708.3(BCDIN3D):c.605G>A (p.Cys202Tyr)	not specified [RCV004101457]	uncertain significance	12	49838645	49838645	Human		name
156263403	CV2282573	single nucleotide variant	NM_181708.3(BCDIN3D):c.744T>G (p.Cys248Trp)	not specified [RCV004135141]	uncertain significance	12	49838506	49838506	Human		name
156151739	CV2307580	single nucleotide variant	NM_181708.3(BCDIN3D):c.376C>T (p.Pro126Ser)	not specified [RCV004168008]	uncertain significance	12	49838874	49838874	Human		name
155983633	CV2367796	single nucleotide variant	NM_181708.3(BCDIN3D):c.773G>A (p.Ser258Asn)	not specified [RCV004222912]	uncertain significance	12	49838477	49838477	Human		name
156269897	CV2398631	single nucleotide variant	NM_181708.3(BCDIN3D):c.598T>C (p.Trp200Arg)	not specified [RCV004237938]	uncertain significance	12	49838652	49838652	Human		name
329375929	CV2441208	single nucleotide variant	NM_181708.3(BCDIN3D):c.572A>G (p.His191Arg)	not specified [RCV004263603]	likely benign	12	49838678	49838678	Human		name
407495405	CV3417650	single nucleotide variant	NM_181708.3(BCDIN3D):c.319C>T (p.Leu107Phe)	not specified [RCV004605817]	uncertain significance	12	49838931	49838931	Human		name
597736477	CV3639607	single nucleotide variant	NM_181708.3(BCDIN3D):c.695A>G (p.Asn232Ser)	not specified [RCV004889695]	likely benign	12	49838555	49838555	Human		name
597736488	CV3639609	single nucleotide variant	NM_181708.3(BCDIN3D):c.401T>C (p.Leu134Pro)	not specified [RCV004889697]	uncertain significance	12	49838849	49838849	Human		name
597736494	CV3639610	single nucleotide variant	NM_181708.3(BCDIN3D):c.511C>T (p.His171Tyr)	not specified [RCV004889698]	uncertain significance	12	49838739	49838739	Human		name
597736499	CV3639611	single nucleotide variant	NM_181708.3(BCDIN3D):c.554A>G (p.His185Arg)	not specified [RCV004889699]	uncertain significance	12	49838696	49838696	Human		name
597736509	CV3639613	single nucleotide variant	NM_181708.3(BCDIN3D):c.731T>G (p.Met244Arg)	not specified [RCV004889701]	uncertain significance	12	49838519	49838519	Human		name
598273448	CV3941912	single nucleotide variant	NM_181708.3(BCDIN3D):c.613G>A (p.Ala205Thr)	not specified [RCV005303369]	uncertain significance	12	49838637	49838637	Human		name

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