Fmo1 Variant Search Result - Rat Genome Database

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47 records found for search term Fmo1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15126694	CV778736	single nucleotide variant	NM_001282693.2(FMO1):c.485-10T>C	not provided [RCV000963783]	benign	1	171278719	171278719	Human		name
329398418	CV2464555	single nucleotide variant	NM_001282693.2(FMO1):c.5C>T (p.Ala2Val)	not specified [RCV004278250]	uncertain significance	1	171258092	171258092	Human		name
401781982	CV2690037	single nucleotide variant	NM_001282693.2(FMO1):c.11G>A (p.Arg4Gln)	not specified [RCV004299911]	uncertain significance	1	171258098	171258098	Human		name
401866477	CV2775562	single nucleotide variant	NM_001282693.2(FMO1):c.19A>G (p.Ile7Val)	not specified [RCV004350730]	uncertain significance	1	171258106	171258106	Human		name
8624801	CV79915	single nucleotide variant	NM_002021.2(FMO1):c.584C>T (p.Ser195Phe)	Malignant melanoma [RCV000059991]	not provided	1	171278828	171278828	Human		name
401763370	CV2714531	single nucleotide variant	NM_001282693.2(FMO1):c.67G>A (p.Glu23Lys)	not specified [RCV004318048]	uncertain significance	1	171258154	171258154	Human		name
401933163	CV2806159	single nucleotide variant	NM_001282693.2(FMO1):c.660G>A (p.Val220=)	not provided [RCV003409245]	likely benign	1	171280818	171280818	Human		name
407510052	CV3432444	single nucleotide variant	NM_001282693.2(FMO1):c.31G>C (p.Gly11Arg)	not specified [RCV004625964]	uncertain significance	1	171258118	171258118	Human		name
156112923	CV2263705	single nucleotide variant	NM_001282693.2(FMO1):c.160C>A (p.Leu54Ile)	not specified [RCV004135997]	uncertain significance	1	171267570	171267570	Human		name
155906969	CV2379176	single nucleotide variant	NM_001282693.2(FMO1):c.145G>A (p.Glu49Lys)	not specified [RCV004235966]	uncertain significance	1	171267555	171267555	Human		name
401735297	CV2706741	single nucleotide variant	NM_001282693.2(FMO1):c.140T>C (p.Val47Ala)	not specified [RCV004319303]	uncertain significance	1	171267550	171267550	Human		name
401769752	CV2731599	single nucleotide variant	NM_001282693.2(FMO1):c.122G>C (p.Trp41Ser)	not specified [RCV004330944]	uncertain significance	1	171258209	171258209	Human		name
401884390	CV2761708	single nucleotide variant	NM_001282693.2(FMO1):c.208T>C (p.Ser70Pro)	not specified [RCV004337323]	uncertain significance	1	171267618	171267618	Human		name
598214858	CV3973455	single nucleotide variant	NM_001282693.2(FMO1):c.257A>T (p.Gln86Leu)	not specified [RCV005339592]	likely benign	1	171267667	171267667	Human		name
155961645	CV2200710	single nucleotide variant	NM_001282693.2(FMO1):c.516T>A (p.His172Gln)	not specified [RCV004081364]	uncertain significance	1	171278760	171278760	Human		name
156273419	CV2202498	single nucleotide variant	NM_001282693.2(FMO1):c.378G>T (p.Glu126Asp)	not specified [RCV004080797]	uncertain significance	1	171275402	171275402	Human		name
156276643	CV2276852	single nucleotide variant	NM_001282693.2(FMO1):c.455A>G (p.Asn152Ser)	not specified [RCV004140198]	uncertain significance	1	171275479	171275479	Human		name
156341671	CV2344889	single nucleotide variant	NM_001282693.2(FMO1):c.521G>A (p.Arg174Gln)	not specified [RCV004191027]	uncertain significance	1	171278765	171278765	Human		name
329377148	CV2435825	single nucleotide variant	NM_001282693.2(FMO1):c.779T>C (p.Ile260Thr)	not specified [RCV004255065]	uncertain significance	1	171280937	171280937	Human		name
401891047	CV2768954	single nucleotide variant	NM_001282693.2(FMO1):c.674T>C (p.Phe225Ser)	not specified [RCV004347050]	uncertain significance	1	171280832	171280832	Human		name
405728301	CV3257315	single nucleotide variant	NM_001282693.2(FMO1):c.494C>T (p.Ala165Val)	not specified [RCV004389673]	uncertain significance	1	171278738	171278738	Human		name
405728309	CV3257316	single nucleotide variant	NM_001282693.2(FMO1):c.520C>T (p.Arg174Trp)	not specified [RCV004389674]	uncertain significance	1	171278764	171278764	Human		name
405728316	CV3257317	single nucleotide variant	NM_001282693.2(FMO1):c.688C>A (p.Pro230Thr)	not specified [RCV004389675]	uncertain significance	1	171280846	171280846	Human		name
407510055	CV3432445	single nucleotide variant	NM_001282693.2(FMO1):c.640A>G (p.Thr214Ala)	not specified [RCV004625965]	uncertain significance	1	171280798	171280798	Human		name
597702013	CV3676550	single nucleotide variant	NM_001282693.2(FMO1):c.347G>A (p.Cys116Tyr)	not specified [RCV004916516]	uncertain significance	1	171275371	171275371	Human		name
597702043	CV3676553	single nucleotide variant	NM_001282693.2(FMO1):c.355T>C (p.Ser119Pro)	not specified [RCV004916519]	uncertain significance	1	171275379	171275379	Human		name
597702050	CV3676554	single nucleotide variant	NM_001282693.2(FMO1):c.962C>G (p.Pro321Arg)	not specified [RCV004916520]	uncertain significance	1	171282112	171282112	Human		name
598214852	CV3973454	single nucleotide variant	NM_001282693.2(FMO1):c.316T>C (p.Phe106Leu)	not specified [RCV005339591]	uncertain significance	1	171267726	171267726	Human		name
598214865	CV3973456	single nucleotide variant	NM_001282693.2(FMO1):c.550G>A (p.Asp184Asn)	not specified [RCV005339593]	uncertain significance	1	171278794	171278794	Human		name
15126700	CV706873	single nucleotide variant	NM_001282693.2(FMO1):c.979T>C (p.Phe327Leu)	not provided [RCV000963784]	benign	1	171282129	171282129	Human		name
15170034	CV731874	single nucleotide variant	NM_001282693.2(FMO1):c.752T>C (p.Ile251Thr)	not provided [RCV000905186]	likely benign	1	171280910	171280910	Human		name
155953784	CV2274245	single nucleotide variant	NM_001282693.2(FMO1):c.1559T>G (p.Phe520Cys)	not specified [RCV004136648]	uncertain significance	1	171285504	171285504	Human		name
156270451	CV2315533	single nucleotide variant	NM_001282693.2(FMO1):c.1297A>T (p.Ile433Phe)	not specified [RCV004169580]	uncertain significance	1	171285242	171285242	Human		name
155914410	CV2341993	single nucleotide variant	NM_001282693.2(FMO1):c.1058A>G (p.Tyr353Cys)	not specified [RCV004184933]	uncertain significance	1	171282208	171282208	Human		name
401732244	CV2678043	single nucleotide variant	NM_001282693.2(FMO1):c.1325A>G (p.Tyr442Cys)	not specified [RCV004296566]	uncertain significance	1	171285270	171285270	Human		name
401766961	CV2680207	single nucleotide variant	NM_001282693.2(FMO1):c.1420C>T (p.Arg474Cys)	not specified [RCV004286682]	uncertain significance	1	171285365	171285365	Human		name
401735062	CV2699151	single nucleotide variant	NM_001282693.2(FMO1):c.1221G>C (p.Glu407Asp)	not specified [RCV004303652]	uncertain significance	1	171283181	171283181	Human		name
401737093	CV2717942	single nucleotide variant	NM_001282693.2(FMO1):c.1382T>C (p.Leu461Pro)	not specified [RCV004321900]	uncertain significance	1	171285327	171285327	Human		name
401725138	CV2725715	single nucleotide variant	NM_001282693.2(FMO1):c.1354A>G (p.Met452Val)	not specified [RCV004322410]	uncertain significance	1	171285299	171285299	Human		name
405728286	CV3257313	single nucleotide variant	NM_001282693.2(FMO1):c.1160G>C (p.Arg387Pro)	not specified [RCV004389671]	uncertain significance	1	171282310	171282310	Human		name
405728294	CV3257314	single nucleotide variant	NM_001282693.2(FMO1):c.1481G>A (p.Arg494Gln)	not specified [RCV004389672]	uncertain significance	1	171285426	171285426	Human		name
597702023	CV3676551	single nucleotide variant	NM_001282693.2(FMO1):c.1516G>C (p.Glu506Gln)	not specified [RCV004916517]	uncertain significance	1	171285461	171285461	Human		name
597702032	CV3676552	single nucleotide variant	NM_001282693.2(FMO1):c.1202C>T (p.Pro401Leu)	not specified [RCV004916518]	uncertain significance	1	171283162	171283162	Human		name
598214846	CV3973453	single nucleotide variant	NM_001282693.2(FMO1):c.1417T>C (p.Phe473Leu)	not specified [RCV005339590]	uncertain significance	1	171285362	171285362	Human		name
598214870	CV3973457	single nucleotide variant	NM_001282693.2(FMO1):c.1492G>C (p.Val498Leu)	not specified [RCV005339594]	uncertain significance	1	171285437	171285437	Human		name
15126705	CV706874	single nucleotide variant	NM_001282693.2(FMO1):c.1118A>G (p.Lys373Arg)	not provided [RCV000963785]	benign	1	171282268	171282268	Human		name
15145293	CV745847	single nucleotide variant	NM_001282693.2(FMO1):c.1078C>T (p.His360Tyr)	not provided [RCV000922517]	likely benign	1	171282228	171282228	Human		name

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