Spem1 Variant Search Result - Rat Genome Database

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49 records found for search term Spem1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156346027	CV2309009	single nucleotide variant	NM_199339.3(SPEM1):c.9G>C (p.Met3Ile)	not specified [RCV004171071]	uncertain significance	17	7420393	7420393	Human		name
597742817	CV3608278	single nucleotide variant	NM_199339.3(SPEM1):c.8T>C (p.Met3Thr)	not specified [RCV004865154]	uncertain significance	17	7420392	7420392	Human		name
405718479	CV3323018	single nucleotide variant	NM_199339.3(SPEM1):c.73C>G (p.Leu25Val)	not specified [RCV004462807]	uncertain significance	17	7420457	7420457	Human		name
407511225	CV3477777	single nucleotide variant	NM_199339.3(SPEM1):c.65G>T (p.Cys22Phe)	not specified [RCV004673012]	uncertain significance	17	7420449	7420449	Human		name
407525612	CV3477778	single nucleotide variant	NM_199339.3(SPEM1):c.43C>G (p.His15Asp)	not specified [RCV004679342]	uncertain significance	17	7420427	7420427	Human		name
156270197	CV2195144	single nucleotide variant	NM_199339.3(SPEM1):c.152G>T (p.Ser51Ile)	not specified [RCV004080093]	uncertain significance	17	7420634	7420634	Human		name
156326538	CV2219628	single nucleotide variant	NM_199339.3(SPEM1):c.101G>T (p.Gly34Val)	not specified [RCV004093739]	uncertain significance	17	7420485	7420485	Human		name
156146432	CV2357934	single nucleotide variant	NM_199339.3(SPEM1):c.179T>C (p.Val60Ala)	not specified [RCV004209717]	uncertain significance	17	7420661	7420661	Human	1	name
155989969	CV2371993	single nucleotide variant	NM_199339.3(SPEM1):c.257A>G (p.Gln86Arg)	not specified [RCV004221668]	uncertain significance	17	7420932	7420932	Human		name
405718416	CV3323012	single nucleotide variant	NM_199339.3(SPEM1):c.161G>A (p.Arg54His)	not specified [RCV004462801]	uncertain significance	17	7420643	7420643	Human		name
405852942	CV3393371	single nucleotide variant	NM_199339.3(SPEM1):c.118A>G (p.Asn40Asp)	not provided [RCV004546101]	likely benign	17	7420502	7420502	Human		name
156071350	CV2229176	single nucleotide variant	NM_199339.3(SPEM1):c.596G>C (p.Gly199Ala)	not specified [RCV004101003]	uncertain significance	17	7421271	7421271	Human		name
156199961	CV2237631	single nucleotide variant	NM_199339.3(SPEM1):c.314C>T (p.Ser105Phe)	not specified [RCV004106562]	uncertain significance	17	7420989	7420989	Human		name
156064306	CV2240217	single nucleotide variant	NM_199339.3(SPEM1):c.911G>A (p.Arg304His)	not specified [RCV004112791]	uncertain significance	17	7421586	7421586	Human		name
156235734	CV2245458	single nucleotide variant	NM_199339.3(SPEM1):c.643G>C (p.Glu215Gln)	not specified [RCV004109238]	likely benign	17	7421318	7421318	Human		name
155983879	CV2275242	single nucleotide variant	NM_199339.3(SPEM1):c.359G>A (p.Arg120His)	not specified [RCV004137027]	likely benign	17	7421034	7421034	Human		name
156001118	CV2296377	single nucleotide variant	NM_199339.3(SPEM1):c.663C>A (p.Asn221Lys)	not specified [RCV004148130]	uncertain significance	17	7421338	7421338	Human		name
156396469	CV2326289	single nucleotide variant	NM_199339.3(SPEM1):c.815G>A (p.Arg272Gln)	not specified [RCV004180535]	uncertain significance	17	7421490	7421490	Human		name
156326411	CV2335458	single nucleotide variant	NM_199339.3(SPEM1):c.340C>T (p.Arg114Cys)	not specified [RCV004187003]	uncertain significance	17	7421015	7421015	Human		name
156200428	CV2362944	single nucleotide variant	NM_199339.3(SPEM1):c.341G>A (p.Arg114His)	not specified [RCV004209046]	likely benign	17	7421016	7421016	Human		name
155986234	CV2363626	single nucleotide variant	NM_199339.3(SPEM1):c.305T>C (p.Met102Thr)	not specified [RCV004216579]	uncertain significance	17	7420980	7420980	Human		name
156034961	CV2376726	single nucleotide variant	NM_199339.3(SPEM1):c.575C>T (p.Thr192Ile)	not specified [RCV004227010]	uncertain significance	17	7421250	7421250	Human		name
329362511	CV2463952	single nucleotide variant	NM_199339.3(SPEM1):c.409C>T (p.Pro137Ser)	not specified [RCV004273671]	uncertain significance	17	7421084	7421084	Human		name
329353207	CV2468936	single nucleotide variant	NM_199339.3(SPEM1):c.898A>C (p.Asn300His)	not specified [RCV004274204]	uncertain significance	17	7421573	7421573	Human		name
401757527	CV2675358	single nucleotide variant	NM_199339.3(SPEM1):c.764G>A (p.Arg255His)	not specified [RCV004292166]	uncertain significance	17	7421439	7421439	Human		name
401736675	CV2683081	single nucleotide variant	NM_199339.3(SPEM1):c.639C>G (p.Ser213Arg)	not specified [RCV004283855]	uncertain significance	17	7421314	7421314	Human		name
401759924	CV2701786	single nucleotide variant	NM_199339.3(SPEM1):c.719C>T (p.Ala240Val)	not specified [RCV004314180]	uncertain significance	17	7421394	7421394	Human		name
401777516	CV2718231	single nucleotide variant	NM_199339.3(SPEM1):c.806G>C (p.Arg269Pro)	not specified [RCV004316223]	uncertain significance	17	7421481	7421481	Human		name
401781575	CV2731695	single nucleotide variant	NM_199339.3(SPEM1):c.763C>T (p.Arg255Cys)	not specified [RCV004331798]	uncertain significance	17	7421438	7421438	Human		name
405718428	CV3323013	single nucleotide variant	NM_199339.3(SPEM1):c.323C>A (p.Pro108Gln)	not specified [RCV004462802]	uncertain significance	17	7420998	7420998	Human		name
405718440	CV3323014	single nucleotide variant	NM_199339.3(SPEM1):c.331C>A (p.Arg111Ser)	not specified [RCV004462803]	uncertain significance	17	7421006	7421006	Human		name
405718449	CV3323015	single nucleotide variant	NM_199339.3(SPEM1):c.337C>T (p.Arg113Cys)	not specified [RCV004462804]	uncertain significance	17	7421012	7421012	Human		name
405718456	CV3323016	single nucleotide variant	NM_199339.3(SPEM1):c.365C>T (p.Ala122Val)	not specified [RCV004462805]	uncertain significance	17	7421040	7421040	Human		name
405718486	CV3323019	single nucleotide variant	NM_199339.3(SPEM1):c.758G>A (p.Arg253Gln)	not specified [RCV004462808]	likely benign	17	7421433	7421433	Human		name
405718495	CV3323020	single nucleotide variant	NM_199339.3(SPEM1):c.793C>T (p.Arg265Trp)	not specified [RCV004462809]	uncertain significance	17	7421468	7421468	Human		name
405718504	CV3323021	single nucleotide variant	NM_199339.3(SPEM1):c.892A>T (p.Ser298Cys)	not specified [RCV004462810]	uncertain significance	17	7421567	7421567	Human		name
405852852	CV3393278	single nucleotide variant	NM_199339.3(SPEM1):c.883G>A (p.Glu295Lys)	not provided [RCV004546008]	likely benign	17	7421558	7421558	Human		name
407511220	CV3477774	single nucleotide variant	NM_199339.3(SPEM1):c.826C>T (p.Arg276Trp)	not specified [RCV004673010]	uncertain significance	17	7421501	7421501	Human		name
407511223	CV3477775	single nucleotide variant	NM_199339.3(SPEM1):c.355A>C (p.Thr119Pro)	not specified [RCV004673011]	uncertain significance	17	7421030	7421030	Human		name
407525610	CV3477776	single nucleotide variant	NM_199339.3(SPEM1):c.358C>T (p.Arg120Cys)	not specified [RCV004679341]	uncertain significance	17	7421033	7421033	Human		name
597768209	CV3608275	single nucleotide variant	NM_199339.3(SPEM1):c.413A>G (p.His138Arg)	not specified [RCV004870993]	uncertain significance	17	7421088	7421088	Human		name
597768215	CV3608276	single nucleotide variant	NM_199339.3(SPEM1):c.629C>A (p.Pro210Gln)	not specified [RCV004870994]	uncertain significance	17	7421304	7421304	Human		name
597742811	CV3608277	single nucleotide variant	NM_199339.3(SPEM1):c.488C>T (p.Thr163Ile)	not specified [RCV004865153]	uncertain significance	17	7421163	7421163	Human		name
598262854	CV3919149	single nucleotide variant	NM_199339.3(SPEM1):c.403G>A (p.Glu135Lys)	not specified [RCV005280310]	uncertain significance	17	7421078	7421078	Human		name
598262857	CV3919150	single nucleotide variant	NM_199339.3(SPEM1):c.677C>T (p.Ala226Val)	not specified [RCV005280311]	uncertain significance	17	7421352	7421352	Human		name
598262860	CV3919151	single nucleotide variant	NM_199339.3(SPEM1):c.664G>A (p.Gly222Ser)	not specified [RCV005280312]	likely benign	17	7421339	7421339	Human		name
598262862	CV3919153	single nucleotide variant	NM_199339.3(SPEM1):c.490T>C (p.Trp164Arg)	not specified [RCV005280313]	uncertain significance	17	7421165	7421165	Human		name
15152377	CV715682	single nucleotide variant	NM_199339.3(SPEM1):c.553G>A (p.Val185Ile)	not provided [RCV000968338]	benign	17	7421228	7421228	Human		name
8636367	CV91590	single nucleotide variant	NM_199339.2(SPEM1):c.839C>T (p.Ala280Val)	Malignant melanoma [RCV000071688]	not provided	17	7421514	7421514	Human		name

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