Bst1 Variant Search Result - Rat Genome Database

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41 records found for search term Bst1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597784278	CV3646968	single nucleotide variant	NM_004334.3(BST1):c.4G>A (p.Ala2Thr)	not specified [RCV004900467]	uncertain significance	4	15703148	15703148	Human		name
405709912	CV3298480	single nucleotide variant	NM_004334.3(BST1):c.26C>G (p.Ser9Trp)	not specified [RCV004426650]	uncertain significance	4	15703170	15703170	Human		name
405709930	CV3298482	single nucleotide variant	NM_004334.3(BST1):c.58C>T (p.Leu20Phe)	not specified [RCV004426652]	uncertain significance	4	15703202	15703202	Human		name
405709938	CV3298483	single nucleotide variant	NM_004334.3(BST1):c.92G>C (p.Arg31Pro)	not specified [RCV004426653]	likely benign	4	15703236	15703236	Human		name
597784251	CV3646961	single nucleotide variant	NM_004334.3(BST1):c.88G>A (p.Ala30Thr)	not specified [RCV004900461]	uncertain significance	4	15703232	15703232	Human		name
597784269	CV3646965	single nucleotide variant	NM_004334.3(BST1):c.56T>G (p.Leu19Arg)	not specified [RCV004900465]	uncertain significance	4	15703200	15703200	Human		name
598175278	CV3939187	single nucleotide variant	NM_004334.3(BST1):c.80C>T (p.Ala27Val)	not specified [RCV005309831]	uncertain significance	4	15703224	15703224	Human		name
15199642	CV720810	single nucleotide variant	NM_004334.3(BST1):c.435A>G (p.Arg145=)	not provided [RCV000890689]	benign	4	15707630	15707630	Human		name
15183870	CV764364	single nucleotide variant	NM_004334.3(BST1):c.663A>G (p.Arg221=)	not provided [RCV000930682]	likely benign	4	15715758	15715758	Human		name
155962806	CV2285697	single nucleotide variant	NM_004334.3(BST1):c.184C>G (p.Gln62Glu)	not specified [RCV004141545]	uncertain significance	4	15703328	15703328	Human		name
405709895	CV3298477	single nucleotide variant	NM_004334.3(BST1):c.143T>C (p.Leu48Pro)	not specified [RCV004426647]	uncertain significance	4	15703287	15703287	Human		name
405709902	CV3298478	single nucleotide variant	NM_004334.3(BST1):c.157G>A (p.Glu53Lys)	not specified [RCV004426648]	uncertain significance	4	15703301	15703301	Human		name
405709908	CV3298479	single nucleotide variant	NM_004334.3(BST1):c.260C>T (p.Pro87Leu)	not specified [RCV004426649]	uncertain significance	4	15705586	15705586	Human		name
407488816	CV3421618	single nucleotide variant	NM_004334.3(BST1):c.260C>A (p.Pro87His)	not specified [RCV004604041]	uncertain significance	4	15705586	15705586	Human		name
597784246	CV3646960	single nucleotide variant	NM_004334.3(BST1):c.149G>C (p.Arg50Pro)	not specified [RCV004900460]	uncertain significance	4	15703293	15703293	Human		name
597784265	CV3646964	single nucleotide variant	NM_004334.3(BST1):c.112G>A (p.Gly38Ser)	not specified [RCV004900464]	uncertain significance	4	15703256	15703256	Human		name
156172174	CV2194207	single nucleotide variant	NM_004334.3(BST1):c.520A>G (p.Arg174Gly)	not specified [RCV004079333]	uncertain significance	4	15711875	15711875	Human		name
156007592	CV2299744	single nucleotide variant	NM_004334.3(BST1):c.869A>C (p.Gln290Pro)	not specified [RCV004148905]	uncertain significance	4	15731757	15731757	Human		name
156242475	CV2306553	single nucleotide variant	NM_004334.3(BST1):c.553G>C (p.Gly185Arg)	not specified [RCV004157161]	uncertain significance	4	15715303	15715303	Human		name
156364208	CV2341869	single nucleotide variant	NM_004334.3(BST1):c.662G>A (p.Arg221Gln)	not specified [RCV004184819]	uncertain significance	4	15715757	15715757	Human		name
156077433	CV2351036	single nucleotide variant	NM_004334.3(BST1):c.797T>G (p.Val266Gly)	not specified [RCV004211859]	uncertain significance	4	15722880	15722880	Human		name
156336219	CV2360698	single nucleotide variant	NM_004334.3(BST1):c.358G>A (p.Ala120Thr)	not specified [RCV004213491]	uncertain significance	4	15707553	15707553	Human		name
155939116	CV2375710	single nucleotide variant	NM_004334.3(BST1):c.440A>G (p.Lys147Arg)	not specified [RCV004224307]	uncertain significance	4	15707635	15707635	Human		name
155927039	CV2395948	single nucleotide variant	NM_004334.3(BST1):c.373C>T (p.Arg125Cys)	not specified [RCV004237501]	uncertain significance	4	15707568	15707568	Human		name
329370804	CV2461822	single nucleotide variant	NM_004334.3(BST1):c.390C>G (p.Ser130Arg)	not specified [RCV004271742]	uncertain significance	4	15707585	15707585	Human		name
401721086	CV2673595	single nucleotide variant	NM_004334.3(BST1):c.499C>G (p.Pro167Ala)	not specified [RCV004282333]	likely benign	4	15711854	15711854	Human		name
401770537	CV2707270	single nucleotide variant	NM_004334.3(BST1):c.590C>T (p.Thr197Ile)	not specified [RCV004310887]	uncertain significance	4	15715340	15715340	Human		name
401782870	CV2707553	single nucleotide variant	NM_004334.3(BST1):c.309A>C (p.Arg103Ser)	not specified [RCV004312920]	uncertain significance	4	15705635	15705635	Human		name
401732686	CV2708938	single nucleotide variant	NM_004334.3(BST1):c.697C>T (p.Pro233Ser)	not specified [RCV004309906]	uncertain significance	4	15715792	15715792	Human		name
401863066	CV2765902	single nucleotide variant	NM_004334.3(BST1):c.550T>C (p.Ser184Pro)	not specified [RCV004337932]	uncertain significance	4	15715300	15715300	Human		name
405709919	CV3298481	single nucleotide variant	NM_004334.3(BST1):c.371G>A (p.Arg124His)	not specified [RCV004426651]	uncertain significance	4	15707566	15707566	Human		name
407500595	CV3421619	single nucleotide variant	NM_004334.3(BST1):c.920C>G (p.Pro307Arg)	not specified [RCV004607168]	uncertain significance	4	15731808	15731808	Human		name
597784255	CV3646962	single nucleotide variant	NM_004334.3(BST1):c.757A>G (p.Met253Val)	not specified [RCV004900462]	uncertain significance	4	15718959	15718959	Human		name
597749658	CV3646966	single nucleotide variant	NM_004334.3(BST1):c.382C>G (p.Pro128Ala)	not specified [RCV004892401]	uncertain significance	4	15707577	15707577	Human		name
597784273	CV3646967	single nucleotide variant	NM_004334.3(BST1):c.639C>A (p.Asn213Lys)	not specified [RCV004900466]	uncertain significance	4	15715734	15715734	Human		name
598211127	CV3939188	single nucleotide variant	NM_004334.3(BST1):c.871A>G (p.Arg291Gly)	not specified [RCV005315965]	uncertain significance	4	15731759	15731759	Human		name
15165779	CV698405	single nucleotide variant	NM_004334.3(BST1):c.301A>G (p.Ile101Val)	not provided [RCV000948674]	benign	4	15705627	15705627	Human		name
15156898	CV698407	single nucleotide variant	NM_004334.3(BST1):c.715G>A (p.Gly239Arg)	not provided [RCV000946785]	benign	4	15718917	15718917	Human		name
15165330	CV709210	single nucleotide variant	NM_004334.3(BST1):c.694G>A (p.Gly232Arg)	not provided [RCV000970925]	likely benign	4	15715789	15715789	Human		name
15147622	CV748785	single nucleotide variant	NM_004334.3(BST1):c.370C>T (p.Arg124Cys)	not provided [RCV000922942]	benign	4	15707565	15707565	Human		name
8631047	CV86203	single nucleotide variant	NM_004334.2(BST1):c.527C>T (p.Ser176Phe)	Malignant melanoma [RCV000066294]	not provided	4	15711882	15711882	Human		name

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