Cyp8b1 Variant Search Result - Rat Genome Database

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46 records found for search term Cyp8b1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156076582	CV2350967	single nucleotide variant	NM_004391.3(CYP8B1):c.82C>T (p.Arg28Cys)	not specified [RCV004211795]	uncertain significance	3	42875735	42875735	Human		name
15170618	CV698093	single nucleotide variant	NM_004391.3(CYP8B1):c.798G>T (p.Gly266=)	not provided [RCV000949684]	benign	3	42875019	42875019	Human		name
15166258	CV720442	single nucleotide variant	NM_004391.3(CYP8B1):c.430C>T (p.Leu144=)	not provided [RCV000882593]	benign	3	42875387	42875387	Human		name
8630833	CV85988	single nucleotide variant	NM_004391.2(CYP8B1):c.789G>A (p.Arg263=)	Malignant melanoma [RCV000066072]	not provided	3	42875028	42875028	Human		name
156150518	CV2235046	single nucleotide variant	NM_004391.3(CYP8B1):c.238G>A (p.Val80Ile)	not specified [RCV004113229]	uncertain significance	3	42875579	42875579	Human		name
156269904	CV2326416	single nucleotide variant	NM_004391.3(CYP8B1):c.212A>T (p.Gln71Leu)	not specified [RCV004182989]	uncertain significance	3	42875605	42875605	Human		name
156182382	CV2353150	single nucleotide variant	NM_004391.3(CYP8B1):c.109A>G (p.Lys37Glu)	not provided [RCV004695648]\|not specified [RCV004203625]	uncertain significance	3	42875708	42875708	Human		name
401722351	CV2706481	single nucleotide variant	NM_004391.3(CYP8B1):c.161T>C (p.Phe54Ser)	not specified [RCV004317298]	uncertain significance	3	42875656	42875656	Human		name
401926343	CV2827305	single nucleotide variant	NM_004391.3(CYP8B1):c.1308C>A (p.Gly436=)	not provided [RCV003437784]	likely benign	3	42874509	42874509	Human		name
401922204	CV2827306	single nucleotide variant	NM_004391.3(CYP8B1):c.1245G>A (p.Arg415=)	not provided [RCV003433538]	likely benign	3	42874572	42874572	Human		name
407452683	CV3420271	single nucleotide variant	NM_004391.3(CYP8B1):c.205A>G (p.Thr69Ala)	not specified [RCV004608620]	uncertain significance	3	42875612	42875612	Human		name
597673252	CV3654962	single nucleotide variant	NM_004391.3(CYP8B1):c.143C>T (p.Ala48Val)	not specified [RCV004913460]	uncertain significance	3	42875674	42875674	Human		name
598250300	CV3952646	single nucleotide variant	NM_004391.3(CYP8B1):c.199G>A (p.Val67Met)	not specified [RCV005322867]	uncertain significance	3	42875618	42875618	Human		name
598250307	CV3952647	single nucleotide variant	NM_004391.3(CYP8B1):c.194G>T (p.Gly65Val)	not specified [RCV005322868]	uncertain significance	3	42875623	42875623	Human		name
15097815	CV720441	single nucleotide variant	NM_004391.3(CYP8B1):c.1071C>T (p.Leu357=)	not provided [RCV000891590]	benign	3	42874746	42874746	Human		name
156249443	CV2215557	single nucleotide variant	NM_004391.3(CYP8B1):c.724G>A (p.Val242Met)	not specified [RCV004089329]	uncertain significance	3	42875093	42875093	Human		name
156005294	CV2281497	single nucleotide variant	NM_004391.3(CYP8B1):c.474T>A (p.Ser158Arg)	not specified [RCV004153814]	uncertain significance	3	42875343	42875343	Human		name
156053201	CV2329076	single nucleotide variant	NM_004391.3(CYP8B1):c.376G>A (p.Ala126Thr)	not specified [RCV004180346]	uncertain significance	3	42875441	42875441	Human		name
156216868	CV2348068	single nucleotide variant	NM_004391.3(CYP8B1):c.692G>A (p.Arg231Gln)	not specified [RCV004197749]	uncertain significance	3	42875125	42875125	Human		name
155902239	CV2378460	single nucleotide variant	NM_004391.3(CYP8B1):c.598G>A (p.Gly200Arg)	not specified [RCV004228518]	uncertain significance	3	42875219	42875219	Human		name
401759536	CV2712537	single nucleotide variant	NM_004391.3(CYP8B1):c.351A>C (p.Gln117His)	not specified [RCV004307873]	uncertain significance	3	42875466	42875466	Human		name
401882196	CV2781559	single nucleotide variant	NM_004391.3(CYP8B1):c.594G>T (p.Gln198His)	not specified [RCV004354778]	uncertain significance	3	42875223	42875223	Human		name
405678384	CV3236471	single nucleotide variant	NM_004391.3(CYP8B1):c.559G>C (p.Gly187Arg)	not specified [RCV004370622]	uncertain significance	3	42875258	42875258	Human		name
405678389	CV3236472	single nucleotide variant	NM_004391.3(CYP8B1):c.689G>A (p.Gly230Asp)	not specified [RCV004370623]	uncertain significance	3	42875128	42875128	Human		name
405678394	CV3236473	single nucleotide variant	NM_004391.3(CYP8B1):c.779A>T (p.Gln260Leu)	not specified [RCV004370624]	uncertain significance	3	42875038	42875038	Human		name
407452686	CV3420272	single nucleotide variant	NM_004391.3(CYP8B1):c.460T>C (p.Ser154Pro)	not specified [RCV004608621]	likely benign	3	42875357	42875357	Human		name
597673270	CV3654964	single nucleotide variant	NM_004391.3(CYP8B1):c.392T>C (p.Leu131Pro)	not specified [RCV004913462]	uncertain significance	3	42875425	42875425	Human		name
597673277	CV3654965	single nucleotide variant	NM_004391.3(CYP8B1):c.341G>A (p.Arg114His)	not specified [RCV004913463]	uncertain significance	3	42875476	42875476	Human		name
597673287	CV3654966	single nucleotide variant	NM_004391.3(CYP8B1):c.926G>C (p.Arg309Thr)	not specified [RCV004913464]	uncertain significance	3	42874891	42874891	Human		name
597673297	CV3654967	single nucleotide variant	NM_004391.3(CYP8B1):c.979T>C (p.Phe327Leu)	not specified [RCV004913465]	uncertain significance	3	42874838	42874838	Human		name
15144621	CV708857	single nucleotide variant	NM_004391.3(CYP8B1):c.713A>G (p.Lys238Arg)	not provided [RCV000966862]	benign	3	42875104	42875104	Human		name
156140073	CV2212143	single nucleotide variant	NM_004391.3(CYP8B1):c.1163T>C (p.Leu388Pro)	not specified [RCV004089043]	uncertain significance	3	42874654	42874654	Human		name
155978585	CV2222710	single nucleotide variant	NM_004391.3(CYP8B1):c.1064C>A (p.Thr355Asn)	not specified [RCV004101565]	uncertain significance	3	42874753	42874753	Human		name
156200543	CV2362959	single nucleotide variant	NM_004391.3(CYP8B1):c.1129C>T (p.Arg377Cys)	not specified [RCV004209058]	uncertain significance	3	42874688	42874688	Human		name
156077749	CV2375131	single nucleotide variant	NM_004391.3(CYP8B1):c.1045C>T (p.Arg349Trp)	not specified [RCV004230175]	uncertain significance	3	42874772	42874772	Human		name
401731098	CV2693598	single nucleotide variant	NM_004391.3(CYP8B1):c.1274A>T (p.Lys425Met)	not specified [RCV004297942]	uncertain significance	3	42874543	42874543	Human		name
401783103	CV2716130	single nucleotide variant	NM_004391.3(CYP8B1):c.1174A>G (p.Met392Val)	not specified [RCV004323369]	likely benign	3	42874643	42874643	Human		name
401865597	CV2755564	single nucleotide variant	NM_004391.3(CYP8B1):c.1327A>G (p.Arg443Gly)	not specified [RCV004340143]	uncertain significance	3	42874490	42874490	Human		name
405678376	CV3236469	single nucleotide variant	NM_004391.3(CYP8B1):c.1189C>T (p.His397Tyr)	not specified [RCV004370620]	uncertain significance	3	42874628	42874628	Human		name
405678381	CV3236470	single nucleotide variant	NM_004391.3(CYP8B1):c.1293G>A (p.Met431Ile)	not specified [RCV004370621]	uncertain significance	3	42874524	42874524	Human		name
407452689	CV3420274	single nucleotide variant	NM_004391.3(CYP8B1):c.1180C>T (p.Pro394Ser)	not specified [RCV004608623]	uncertain significance	3	42874637	42874637	Human		name
597673247	CV3654961	single nucleotide variant	NM_004391.3(CYP8B1):c.1219C>T (p.Arg407Cys)	not specified [RCV004913459]	uncertain significance	3	42874598	42874598	Human		name
597673261	CV3654963	single nucleotide variant	NM_004391.3(CYP8B1):c.1084G>A (p.Glu362Lys)	not specified [RCV004913461]	uncertain significance	3	42874733	42874733	Human		name
15164120	CV698092	single nucleotide variant	NM_004391.3(CYP8B1):c.1204G>A (p.Val402Ile)	not provided [RCV000948260]	benign	3	42874613	42874613	Human		name
15113171	CV708856	single nucleotide variant	NM_004391.3(CYP8B1):c.1069C>T (p.Leu357Phe)	not provided [RCV000961439]	benign	3	42874748	42874748	Human		name
8630832	CV85987	single nucleotide variant	NM_004391.2(CYP8B1):c.1468G>A (p.Asp490Asn)	Malignant melanoma [RCV000066071]	not provided	3	42874349	42874349	Human		name

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