Rara Variant Search Result - Rat Genome Database

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34 records found for search term Rara

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15177870	CV778247	single nucleotide variant	NM_000964.4(RARA):c.469+9C>T	not provided [RCV000951141]	benign	17	40349934	40349934	Human		name
15100477	CV731147	single nucleotide variant	NM_000964.4(RARA):c.1013-6C>T	not provided [RCV000892114]	benign	17	40355257	40355257	Human		name
401903929	CV2811313	single nucleotide variant	NM_000964.4(RARA):c.179-3622C>T	not provided [RCV003419725]	benign	17	40344694	40344694	Human		name
15190586	CV727146	single nucleotide variant	NM_000964.4(RARA):c.72C>T (p.Tyr24=)	not provided [RCV000888141]	likely benign	17	40331290	40331290	Human		name
156223740	CV2355603	single nucleotide variant	NM_000964.4(RARA):c.58C>G (p.Pro20Ala)	not specified [RCV004205446]	uncertain significance	17	40331276	40331276	Human		name
329400480	CV2438381	single nucleotide variant	NM_000964.4(RARA):c.35G>C (p.Gly12Ala)	not specified [RCV004259539]	uncertain significance	17	40331253	40331253	Human		name
401874139	CV2754586	single nucleotide variant	NM_000964.4(RARA):c.50A>G (p.Asn17Ser)	not specified [RCV004339263]	uncertain significance	17	40331268	40331268	Human		name
15113425	CV715425	single nucleotide variant	NM_000964.4(RARA):c.837C>T (p.Pro279=)	not provided [RCV000961489]	benign	17	40354331	40354331	Human		name
15134328	CV740716	single nucleotide variant	NM_000964.4(RARA):c.543G>A (p.Thr181=)	not provided [RCV000898269]	likely benign	17	40351983	40351983	Human		name
401723984	CV2737922	single nucleotide variant	NM_000964.4(RARA):c.1011A>C (p.Gly337=)	Mendelian syndromes with cleft lip/palate [RCV003315094]	uncertain significance	17	40354505	40354505	Human		name
15140453	CV755819	single nucleotide variant	NM_000964.4(RARA):c.1299C>T (p.Asp433=)	not provided [RCV000921679]	likely benign	17	40356136	40356136	Human		name
10045346	CV189152	single nucleotide variant	NM_000964.4(RARA):c.826C>T (p.Arg276Trp)	Tretinoin response [RCV000171542]\|not provided [RCV001281697]	drug response\|uncertain significance	17	40354320	40354320	Human		name
329360192	CV2446634	single nucleotide variant	NM_000964.4(RARA):c.824C>T (p.Thr275Met)	not specified [RCV004251522]	uncertain significance	17	40354318	40354318	Human		name
401899981	CV2780143	single nucleotide variant	NM_000964.4(RARA):c.358A>G (p.Met120Val)	not specified [RCV004355799]	uncertain significance	17	40349814	40349814	Human		name
405659406	CV3312197	single nucleotide variant	NM_000964.4(RARA):c.332T>G (p.Phe111Cys)	not specified [RCV004438517]	uncertain significance	17	40349788	40349788	Human		name
405659410	CV3312198	single nucleotide variant	NM_000964.4(RARA):c.536C>T (p.Thr179Met)	not specified [RCV004438518]	uncertain significance	17	40351976	40351976	Human		name
405659412	CV3312199	single nucleotide variant	NM_000964.4(RARA):c.545C>T (p.Pro182Leu)	not specified [RCV004438519]	uncertain significance	17	40351985	40351985	Human		name
407466667	CV3472409	single nucleotide variant	NM_000964.4(RARA):c.703T>A (p.Cys235Ser)	not specified [RCV004660526]	uncertain significance	17	40352403	40352403	Human		name
597783576	CV3592905	single nucleotide variant	NM_000964.4(RARA):c.677A>T (p.Asp226Val)	not specified [RCV004854297]	uncertain significance	17	40352377	40352377	Human		name
597705785	CV3592906	single nucleotide variant	NM_000964.4(RARA):c.969T>G (p.Asp323Glu)	not specified [RCV004860436]	uncertain significance	17	40354463	40354463	Human		name
597783583	CV3592908	single nucleotide variant	NM_000964.4(RARA):c.464A>G (p.Lys155Arg)	not specified [RCV004854299]	uncertain significance	17	40349920	40349920	Human		name
597783685	CV3592909	single nucleotide variant	NM_000964.4(RARA):c.524C>T (p.Ser175Phe)	not specified [RCV004854300]	uncertain significance	17	40351964	40351964	Human		name
40887138	CV974048	single nucleotide variant	NM_000964.4(RARA):c.827G>A (p.Arg276Gln)	Inborn genetic diseases [RCV001266577]\|not provided [RCV002221619]	likely pathogenic\|uncertain significance	17	40354321	40354321	Human	1	name
151736315	CV1354836	single nucleotide variant	NM_000964.4(RARA):c.1181G>A (p.Arg394Gln)	not provided [RCV001892795]	uncertain significance	17	40356018	40356018	Human		name
156153307	CV2394954	single nucleotide variant	NM_000964.4(RARA):c.1283G>T (p.Gly428Val)	not specified [RCV004234602]	uncertain significance	17	40356120	40356120	Human		name
329379361	CV2456222	single nucleotide variant	NM_000964.4(RARA):c.1306G>A (p.Gly436Ser)	not specified [RCV004273406]	uncertain significance	17	40356143	40356143	Human		name
401860839	CV2776216	single nucleotide variant	NM_000964.4(RARA):c.1273G>A (p.Gly425Arg)	not specified [RCV004353293]	uncertain significance	17	40356110	40356110	Human		name
401885782	CV2783385	single nucleotide variant	NM_000964.4(RARA):c.1288G>C (p.Gly430Arg)	not specified [RCV004365738]	uncertain significance	17	40356125	40356125	Human		name
405659401	CV3312195	single nucleotide variant	NM_000964.4(RARA):c.1108C>T (p.Arg370Cys)	not specified [RCV004438515]	uncertain significance	17	40355358	40355358	Human		name
405659404	CV3312196	single nucleotide variant	NM_000964.4(RARA):c.1319C>T (p.Pro440Leu)	not specified [RCV004438516]	uncertain significance	17	40356156	40356156	Human		name
407500645	CV3472410	single nucleotide variant	NM_000964.4(RARA):c.1313C>T (p.Ala438Val)	not specified [RCV004669601]	uncertain significance	17	40356150	40356150	Human		name
597783579	CV3592907	single nucleotide variant	NM_000964.4(RARA):c.1280C>T (p.Pro427Leu)	not specified [RCV004854298]	uncertain significance	17	40356117	40356117	Human		name
598183652	CV3905481	single nucleotide variant	NM_000964.4(RARA):c.1239G>T (p.Met413Ile)	not specified [RCV005265633]	uncertain significance	17	40356076	40356076	Human		name
10045347	CV189153	deletion	NM_000964.4(RARA):c.1226_*1del (p.Leu409_Ter463delinsXaa)	Tretinoin response [RCV000171543]	drug response	17	40356062	40356226	Human		name

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