Faim Variant Search Result - Rat Genome Database

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41 records found for search term Faim

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597718805	CV3671819	single nucleotide variant	NM_001033031.2(FAIM):c.-17+2085A>T	not specified [RCV004918565]	uncertain significance	3	138611022	138611022	Human		name
329385795	CV2432222	single nucleotide variant	NM_001033031.2(FAIM):c.79G>A (p.Val27Ile)	not specified [RCV004251152]	uncertain significance	3	138621441	138621441	Human		name
156073419	CV2365454	single nucleotide variant	NM_001033031.2(FAIM):c.215G>T (p.Gly72Val)	not specified [RCV004209529]	uncertain significance	3	138622225	138622225	Human		name
401718647	CV2704724	single nucleotide variant	NM_001033031.2(FAIM):c.212T>C (p.Val71Ala)	not specified [RCV004307326]	uncertain significance	3	138622222	138622222	Human		name
401733452	CV2713094	single nucleotide variant	NM_001033031.2(FAIM):c.112G>T (p.Val38Phe)	not specified [RCV004316647]	uncertain significance	3	138621474	138621474	Human		name
407507730	CV3435381	single nucleotide variant	NM_001033031.2(FAIM):c.203T>A (p.Phe68Tyr)	not specified [RCV004625186]	uncertain significance	3	138622213	138622213	Human		name
156236873	CV2224160	single nucleotide variant	NM_001033031.2(FAIM):c.519A>G (p.Ile173Met)	not specified [RCV004096012]	uncertain significance	3	138632992	138632992	Human		name
156172003	CV2247483	single nucleotide variant	NM_001033031.2(FAIM):c.481G>A (p.Glu161Lys)	not specified [RCV004108806]	uncertain significance	3	138632954	138632954	Human		name
156199386	CV2255992	single nucleotide variant	NM_001033031.2(FAIM):c.401T>G (p.Val134Gly)	not specified [RCV004122436]	uncertain significance	3	138622411	138622411	Human		name
156194840	CV2347369	single nucleotide variant	NM_001033031.2(FAIM):c.542G>A (p.Arg181Gln)	not specified [RCV004207209]	uncertain significance	3	138633015	138633015	Human		name
155993079	CV2381677	single nucleotide variant	NM_001033031.2(FAIM):c.424G>A (p.Val142Ile)	not specified [RCV004232143]	uncertain significance	3	138629124	138629124	Human		name
329385704	CV2462229	single nucleotide variant	NM_001033031.2(FAIM):c.506A>G (p.His169Arg)	not specified [RCV004266231]	uncertain significance	3	138632979	138632979	Human		name
401745794	CV2695442	single nucleotide variant	NM_001033031.2(FAIM):c.470A>G (p.Asp157Gly)	not specified [RCV004305641]	uncertain significance	3	138632943	138632943	Human		name
401896108	CV2777498	single nucleotide variant	NM_001033031.2(FAIM):c.515A>C (p.Tyr172Ser)	not specified [RCV004356261]	uncertain significance	3	138632988	138632988	Human		name
405724640	CV3249653	single nucleotide variant	NM_001033031.2(FAIM):c.562A>G (p.Thr188Ala)	not specified [RCV004378473]	uncertain significance	3	138633035	138633035	Human		name
405724650	CV3249654	single nucleotide variant	NM_001033031.2(FAIM):c.581G>C (p.Arg194Thr)	not specified [RCV004378474]	uncertain significance	3	138633054	138633054	Human		name
407507727	CV3435380	single nucleotide variant	NM_001033031.2(FAIM):c.367G>T (p.Val123Leu)	not specified [RCV004625185]	uncertain significance	3	138622377	138622377	Human		name
597718797	CV3671818	single nucleotide variant	NM_001033031.2(FAIM):c.541C>T (p.Arg181Trp)	not specified [RCV004918564]	uncertain significance	3	138633014	138633014	Human		name
8654037	CV130612	single nucleotide variant	NM_012306.3(FAIM2):c.801+7387G>T	Lung cancer [RCV000111099]	uncertain significance	12	49879999	49879999	Human		name
405724659	CV3249655	single nucleotide variant	NM_012306.4(FAIM2):c.19T>C (p.Ser7Pro)	not specified [RCV004378475]	uncertain significance	12	49901322	49901322	Human		name
401932113	CV2806979	single nucleotide variant	NM_012306.4(FAIM2):c.327C>T (p.Ile109=)	not provided [RCV003391803]	likely benign	12	49897572	49897572	Human		name
407507740	CV3435384	single nucleotide variant	NM_012306.4(FAIM2):c.49G>A (p.Gly17Arg)	not specified [RCV004625189]	uncertain significance	12	49901292	49901292	Human		name
598223632	CV3965703	single nucleotide variant	NM_012306.4(FAIM2):c.71A>G (p.Glu24Gly)	not specified [RCV005341183]	uncertain significance	12	49901270	49901270	Human		name
156066709	CV2225593	single nucleotide variant	NM_012306.4(FAIM2):c.275G>T (p.Ser92Ile)	not specified [RCV004100966]	uncertain significance	12	49898027	49898027	Human		name
405724668	CV3249656	single nucleotide variant	NM_012306.4(FAIM2):c.235G>A (p.Gly79Ser)	not specified [RCV004378476]	uncertain significance	12	49898067	49898067	Human		name
405724677	CV3249657	single nucleotide variant	NM_012306.4(FAIM2):c.295C>T (p.Arg99Cys)	not specified [RCV004378477]	uncertain significance	12	49898007	49898007	Human		name
597718821	CV3671821	single nucleotide variant	NM_012306.4(FAIM2):c.131G>C (p.Gly44Ala)	not specified [RCV004918567]	uncertain significance	12	49901210	49901210	Human		name
598223626	CV3965702	single nucleotide variant	NM_012306.4(FAIM2):c.247G>A (p.Gly83Arg)	not specified [RCV005341182]	uncertain significance	12	49898055	49898055	Human		name
8634705	CV89925	single nucleotide variant	NM_012306.3(FAIM2):c.118G>A (p.Glu40Lys)	Malignant melanoma [RCV000070022]	not provided	12	49901223	49901223	Human		name
401746982	CV2698753	single nucleotide variant	NM_012306.4(FAIM2):c.737C>T (p.Pro246Leu)	not specified [RCV004301205]	uncertain significance	12	49889117	49889117	Human		name
401759421	CV2701544	single nucleotide variant	NM_012306.4(FAIM2):c.358G>A (p.Val120Ile)	not specified [RCV004313988]	uncertain significance	12	49897541	49897541	Human		name
401889078	CV2761745	single nucleotide variant	NM_012306.4(FAIM2):c.668G>A (p.Cys223Tyr)	not specified [RCV004337353]	uncertain significance	12	49889186	49889186	Human		name
401897348	CV2790046	single nucleotide variant	NM_012306.4(FAIM2):c.299G>A (p.Arg100Gln)	not specified [RCV004363998]	uncertain significance	12	49898003	49898003	Human		name
405724693	CV3249659	single nucleotide variant	NM_012306.4(FAIM2):c.679C>A (p.Leu227Ile)	not specified [RCV004378479]	likely benign	12	49889175	49889175	Human		name
407507733	CV3435382	single nucleotide variant	NM_012306.4(FAIM2):c.782G>T (p.Gly261Val)	not specified [RCV004625187]	uncertain significance	12	49887405	49887405	Human		name
407507737	CV3435383	single nucleotide variant	NM_012306.4(FAIM2):c.493T>C (p.Phe165Leu)	not specified [RCV004625188]	uncertain significance	12	49890715	49890715	Human		name
597718813	CV3671820	single nucleotide variant	NM_012306.4(FAIM2):c.350C>T (p.Thr117Ile)	not specified [RCV004918566]	uncertain significance	12	49897549	49897549	Human		name
597718829	CV3671822	single nucleotide variant	NM_012306.4(FAIM2):c.631G>A (p.Val211Ile)	not specified [RCV004918568]	likely benign	12	49889501	49889501	Human		name
598223638	CV3965704	single nucleotide variant	NM_012306.4(FAIM2):c.668G>T (p.Cys223Phe)	not specified [RCV005341184]	uncertain significance	12	49889186	49889186	Human		name
598223644	CV3965705	single nucleotide variant	NM_012306.4(FAIM2):c.946G>A (p.Glu316Lys)	not specified [RCV005341185]	uncertain significance	12	49870509	49870509	Human		name
8627297	CV82441	single nucleotide variant	NM_012306.3(FAIM2):c.394G>A (p.Asp132Asn)	Malignant melanoma [RCV000062520]	not provided	12	49897071	49897071	Human		name

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