Gpr174 Variant Search Result - Rat Genome Database

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31 records found for search term Gpr174

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150539243	CV1305236	single nucleotide variant	NM_032553.3(GPR174):c.-34C>T	not provided [RCV001766016]	benign	X	79170974	79170974	Human		name
150539245	CV1305238	single nucleotide variant	NM_032553.3(GPR174):c.-17T>C	not provided [RCV001766018]	benign	X	79170991	79170991	Human		name
405255705	CV3210804	single nucleotide variant	NM_032553.3(GPR174):c.222G>A (p.Leu74=)	GPR174-related disorder [RCV003939316]	likely benign	X	79171229	79171229	Human		name , trait , alternate_id
156149834	CV2201043	single nucleotide variant	NM_032553.3(GPR174):c.74C>T (p.Thr25Ile)	not specified [RCV004074805]	uncertain significance	X	79171081	79171081	Human		name
401929056	CV2826565	single nucleotide variant	NM_032553.3(GPR174):c.675A>G (p.Lys225=)	not provided [RCV003439704]	likely benign	X	79171682	79171682	Human		name
405262892	CV3189383	single nucleotide variant	NM_032553.3(GPR174):c.546C>T (p.Ser182=)	GPR174-related disorder [RCV003896617]	likely benign	X	79171553	79171553	Human		name , trait , alternate_id
405258224	CV3208281	single nucleotide variant	NM_032553.3(GPR174):c.606A>G (p.Leu202=)	GPR174-related disorder [RCV003941710]	benign	X	79171613	79171613	Human		name , trait , alternate_id
15154342	CV729717	single nucleotide variant	NM_032553.3(GPR174):c.483C>T (p.Thr161=)	GPR174-related disorder [RCV003948300]\|not provided [RCV000880196]	benign	X	79171490	79171490	Human		name , trait , alternate_id
15184206	CV774255	single nucleotide variant	NM_032553.3(GPR174):c.423C>T (p.Gly141=)	GPR174-related disorder [RCV003942901]\|not provided [RCV000930757]	likely benign	X	79171430	79171430	Human		name , trait , alternate_id
156050090	CV2271854	single nucleotide variant	NM_032553.3(GPR174):c.114A>G (p.Ile38Met)	not specified [RCV004130678]	uncertain significance	X	79171121	79171121	Human		name
156188425	CV2342210	single nucleotide variant	NM_032553.3(GPR174):c.177A>G (p.Ile59Met)	not specified [RCV004191793]	uncertain significance	X	79171184	79171184	Human		name
401775180	CV2692285	single nucleotide variant	NM_032553.3(GPR174):c.148G>A (p.Glu50Lys)	not specified [RCV004310283]	uncertain significance	X	79171155	79171155	Human		name
405292362	CV3192389	single nucleotide variant	NM_032553.3(GPR174):c.263C>A (p.Pro88His)	GPR174-related disorder [RCV003929659]	likely benign	X	79171270	79171270	Human		name , trait , alternate_id
597744952	CV3684908	single nucleotide variant	NM_032553.3(GPR174):c.276G>A (p.Met92Ile)	not specified [RCV004922368]	uncertain significance	X	79171283	79171283	Human		name
155917497	CV2198954	single nucleotide variant	NM_032553.3(GPR174):c.629T>C (p.Leu210Ser)	not specified [RCV004080370]	uncertain significance	X	79171636	79171636	Human		name
156148668	CV2292787	single nucleotide variant	NM_032553.3(GPR174):c.560C>G (p.Thr187Ser)	not specified [RCV004154448]	uncertain significance	X	79171567	79171567	Human		name
156077368	CV2318541	single nucleotide variant	NM_032553.3(GPR174):c.473G>C (p.Ser158Thr)	not specified [RCV004173449]	uncertain significance	X	79171480	79171480	Human		name
401888360	CV2788387	single nucleotide variant	NM_032553.3(GPR174):c.553A>G (p.Met185Val)	not specified [RCV004354924]	uncertain significance	X	79171560	79171560	Human		name
401929053	CV2826564	single nucleotide variant	NM_032553.3(GPR174):c.374G>A (p.Arg125His)	not provided [RCV003439703]	likely benign	X	79171381	79171381	Human		name
405284173	CV3196621	single nucleotide variant	NM_032553.3(GPR174):c.484T>C (p.Ser162Pro)	GPR174-related disorder [RCV003979534]	benign	X	79171491	79171491	Human		name , trait , alternate_id
405738370	CV3255325	single nucleotide variant	NM_032553.3(GPR174):c.841G>T (p.Ala281Ser)	not specified [RCV004390952]	uncertain significance	X	79171848	79171848	Human		name
405738378	CV3255326	single nucleotide variant	NM_032553.3(GPR174):c.873A>G (p.Ile291Met)	not specified [RCV004390953]	uncertain significance	X	79171880	79171880	Human		name
405738386	CV3255327	single nucleotide variant	NM_032553.3(GPR174):c.937C>A (p.Gln313Lys)	not specified [RCV004390954]	uncertain significance	X	79171944	79171944	Human		name
405738391	CV3255328	single nucleotide variant	NM_032553.3(GPR174):c.997T>C (p.Cys333Arg)	not specified [RCV004390955]	uncertain significance	X	79172004	79172004	Human		name
407526438	CV3436677	single nucleotide variant	NM_032553.3(GPR174):c.623C>T (p.Thr208Met)	not specified [RCV004632439]	uncertain significance	X	79171630	79171630	Human		name
407526441	CV3436678	single nucleotide variant	NM_032553.3(GPR174):c.389A>G (p.Lys130Arg)	not specified [RCV004632440]	uncertain significance	X	79171396	79171396	Human		name
597744947	CV3684906	single nucleotide variant	NM_032553.3(GPR174):c.706G>T (p.Ala236Ser)	not specified [RCV004922367]	uncertain significance	X	79171713	79171713	Human		name
597789877	CV3684907	single nucleotide variant	NM_032553.3(GPR174):c.397T>C (p.Tyr133His)	not specified [RCV004933097]	uncertain significance	X	79171404	79171404	Human		name
597744957	CV3684909	single nucleotide variant	NM_032553.3(GPR174):c.341T>C (p.Val114Ala)	not specified [RCV004922369]	uncertain significance	X	79171348	79171348	Human		name
598274414	CV3971164	single nucleotide variant	NM_032553.3(GPR174):c.706G>A (p.Ala236Thr)	not specified [RCV005351409]	uncertain significance	X	79171713	79171713	Human		name
598233879	CV3971165	single nucleotide variant	NM_032553.3(GPR174):c.463C>T (p.Leu155Phe)	not specified [RCV005342821]	uncertain significance	X	79171470	79171470	Human		name

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