Stradb Variant Search Result - Rat Genome Database

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29 records found for search term Stradb

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405779781	CV3330877	single nucleotide variant	NM_018571.6(STRADB):c.94G>T (p.Val32Phe)	not specified [RCV004458455]	uncertain significance	2	201469953	201469953	Human		name
598208239	CV3915998	single nucleotide variant	NM_018571.6(STRADB):c.94G>A (p.Val32Ile)	not specified [RCV005291428]	uncertain significance	2	201469953	201469953	Human		name
15142294	CV733072	single nucleotide variant	NM_018571.6(STRADB):c.540T>C (p.Cys180=)	not provided [RCV000899649]	benign	2	201475734	201475734	Human		name
155928036	CV2280991	single nucleotide variant	NM_018571.6(STRADB):c.137C>T (p.Ala46Val)	not specified [RCV004145492]	uncertain significance	2	201469996	201469996	Human		name
156338787	CV2351478	single nucleotide variant	NM_018571.6(STRADB):c.106A>G (p.Thr36Ala)	not specified [RCV004193162]	uncertain significance	2	201469965	201469965	Human		name
401748299	CV2698343	single nucleotide variant	NM_018571.6(STRADB):c.112T>C (p.Ser38Pro)	not specified [RCV004304885]	uncertain significance	2	201469971	201469971	Human		name
405779758	CV3330873	single nucleotide variant	NM_018571.6(STRADB):c.121C>T (p.Arg41Cys)	not specified [RCV004458451]	uncertain significance	2	201469980	201469980	Human		name
405779764	CV3330874	single nucleotide variant	NM_018571.6(STRADB):c.163G>A (p.Val55Ile)	not specified [RCV004458452]	uncertain significance	2	201470022	201470022	Human		name
405779769	CV3330875	single nucleotide variant	NM_018571.6(STRADB):c.247G>A (p.Gly83Arg)	not specified [RCV004458453]	uncertain significance	2	201473008	201473008	Human		name
156058807	CV2305278	single nucleotide variant	NM_018571.6(STRADB):c.298C>T (p.Arg100Cys)	not specified [RCV004171199]	uncertain significance	2	201473059	201473059	Human		name
156345556	CV2372941	single nucleotide variant	NM_018571.6(STRADB):c.986G>A (p.Arg329Gln)	not specified [RCV004223983]	uncertain significance	2	201478517	201478517	Human		name
156133121	CV2382898	single nucleotide variant	NM_018571.6(STRADB):c.692C>T (p.Pro231Leu)	not specified [RCV004217496]	uncertain significance	2	201477762	201477762	Human		name
155968885	CV2391512	single nucleotide variant	NM_018571.6(STRADB):c.343C>T (p.Arg115Trp)	not specified [RCV004239897]	uncertain significance	2	201474674	201474674	Human		name
401725210	CV2697314	single nucleotide variant	NM_018571.6(STRADB):c.991C>T (p.His331Tyr)	not specified [RCV004304072]	uncertain significance	2	201478522	201478522	Human		name
405779775	CV3330876	single nucleotide variant	NM_018571.6(STRADB):c.472G>A (p.Glu158Lys)	not specified [RCV004458454]	uncertain significance	2	201475666	201475666	Human		name
597758231	CV3615051	single nucleotide variant	NM_018571.6(STRADB):c.629T>A (p.Val210Asp)	not specified [RCV004868760]	uncertain significance	2	201477699	201477699	Human		name
597758236	CV3615052	single nucleotide variant	NM_018571.6(STRADB):c.749A>G (p.Asp250Gly)	not specified [RCV004868761]	uncertain significance	2	201478115	201478115	Human		name
597758241	CV3615053	single nucleotide variant	NM_018571.6(STRADB):c.299G>T (p.Arg100Leu)	not specified [RCV004868762]	uncertain significance	2	201473060	201473060	Human		name
597758246	CV3615054	single nucleotide variant	NM_018571.6(STRADB):c.916T>G (p.Ser306Ala)	not specified [RCV004868763]	uncertain significance	2	201478447	201478447	Human		name
597758259	CV3615056	single nucleotide variant	NM_018571.6(STRADB):c.500G>A (p.Gly167Glu)	not specified [RCV004868765]	uncertain significance	2	201475694	201475694	Human		name
598208231	CV3915996	single nucleotide variant	NM_018571.6(STRADB):c.349C>T (p.Pro117Ser)	not specified [RCV005291426]	uncertain significance	2	201474680	201474680	Human		name
598251806	CV3916000	single nucleotide variant	NM_018571.6(STRADB):c.488A>G (p.Asn163Ser)	not specified [RCV005277964]	uncertain significance	2	201475682	201475682	Human		name
156080810	CV2255964	single nucleotide variant	NM_018571.6(STRADB):c.1016C>T (p.Ser339Phe)	not specified [RCV004122412]	uncertain significance	2	201478547	201478547	Human		name
155977495	CV2342896	single nucleotide variant	NM_018571.6(STRADB):c.1138A>G (p.Ile380Val)	not specified [RCV004189930]	uncertain significance	2	201480056	201480056	Human		name
597758254	CV3615055	single nucleotide variant	NM_018571.6(STRADB):c.1231G>A (p.Glu411Lys)	not specified [RCV004868764]	uncertain significance	2	201480149	201480149	Human		name
598208227	CV3915995	single nucleotide variant	NM_018571.6(STRADB):c.1241C>T (p.Ser414Leu)	not specified [RCV005291425]	uncertain significance	2	201480159	201480159	Human		name
598208243	CV3915999	single nucleotide variant	NM_018571.6(STRADB):c.1075T>G (p.Ser359Ala)	not specified [RCV005291429]	uncertain significance	2	201479493	201479493	Human		name
598251810	CV3916001	single nucleotide variant	NM_018571.6(STRADB):c.1050G>C (p.Leu350Phe)	not specified [RCV005277965]	uncertain significance	2	201478581	201478581	Human		name
8625261	CV80380	single nucleotide variant	NM_018571.5(STRADB):c.1220A>G (p.Asp407Gly)	Malignant melanoma [RCV000060457]	not provided	2	201480138	201480138	Human		name

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