Shmt1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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58 records found for search term Shmt1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15111699	CV760559	single nucleotide variant	NM_004169.5(SHMT1):c.520-6C>G	not provided [RCV000916779]	likely benign	17	18340819	18340819	Human		name
15141093	CV780098	single nucleotide variant	NM_004169.5(SHMT1):c.815-3C>T	not provided [RCV000966250]	benign	17	18335678	18335678	Human		name
15097955	CV731134	single nucleotide variant	NM_004169.5(SHMT1):c.1054+6G>A	not provided [RCV000891623]	likely benign	17	18333160	18333160	Human		name
15119564	CV779921	single nucleotide variant	NM_004169.5(SHMT1):c.242+10T>C	not provided [RCV000962571]	benign	17	18353662	18353662	Human		name
8585272	CV119855	single nucleotide variant	NM_004169.4(SHMT1):c.519+2678C>G	Lung cancer [RCV000100375]	uncertain significance	17	18344818	18344818	Human		name
329392829	CV2439212	single nucleotide variant	NM_004169.5(SHMT1):c.7A>G (p.Met3Val)	not specified [RCV004266483]	uncertain significance	17	18355975	18355975	Human		name
15169129	CV704010	single nucleotide variant	NM_004169.5(SHMT1):c.2T>G (p.Met1Arg)	not provided [RCV000949398]	likely benign	17	18355980	18355980	Human		name
15153652	CV727048	single nucleotide variant	NM_004169.5(SHMT1):c.2T>A (p.Met1Lys)	not provided [RCV000880053]	benign	17	18355980	18355980	Human		name
15118267	CV771306	single nucleotide variant	NM_004169.5(SHMT1):c.40C>T (p.Leu14=)	not provided [RCV000939980]	likely benign	17	18355942	18355942	Human		name
15178773	CV715283	single nucleotide variant	NM_004169.5(SHMT1):c.753G>C (p.Val251=)	not provided [RCV000973746]	benign	17	18340104	18340104	Human		name
15194337	CV755698	single nucleotide variant	NM_004169.5(SHMT1):c.753G>A (p.Val251=)	not provided [RCV000911096]	benign	17	18340104	18340104	Human		name
8636043	CV91266	single nucleotide variant	NM_004169.4(SHMT1):c.594C>T (p.Ile198=)	Malignant melanoma [RCV000071364]	not provided	17	18340739	18340739	Human		name
401889302	CV2759769	single nucleotide variant	NM_004169.5(SHMT1):c.290A>T (p.Gln97Leu)	not specified [RCV004342813]	uncertain significance	17	18348393	18348393	Human		name
405732361	CV3314599	single nucleotide variant	NM_004169.5(SHMT1):c.266T>C (p.Ile89Thr)	not specified [RCV004451184]	uncertain significance	17	18348417	18348417	Human		name
597718606	CV3602683	single nucleotide variant	NM_004169.5(SHMT1):c.265A>G (p.Ile89Val)	not specified [RCV004861779]	uncertain significance	17	18348418	18348418	Human		name
597718675	CV3602690	single nucleotide variant	NM_004169.5(SHMT1):c.236G>A (p.Gly79Asp)	not specified [RCV004861786]	uncertain significance	17	18353678	18353678	Human		name
598242044	CV3914245	single nucleotide variant	NM_004169.5(SHMT1):c.240G>C (p.Gln80His)	not specified [RCV005276453]	uncertain significance	17	18353674	18353674	Human		name
15167134	CV704008	single nucleotide variant	NM_004169.5(SHMT1):c.1380C>T (p.Ala460=)	not provided [RCV000948991]	benign	17	18328822	18328822	Human		name
156333407	CV2214596	single nucleotide variant	NM_004169.5(SHMT1):c.410G>A (p.Arg137His)	not specified [RCV004090432]	uncertain significance	17	18347605	18347605	Human		name
156148508	CV2292746	single nucleotide variant	NM_004169.5(SHMT1):c.934G>A (p.Val312Ile)	not specified [RCV004154412]	uncertain significance	17	18333286	18333286	Human		name
329367863	CV2427617	single nucleotide variant	NM_004169.5(SHMT1):c.343G>A (p.Val115Ile)	not specified [RCV004250249]	uncertain significance	17	18348340	18348340	Human		name
401751426	CV2716383	single nucleotide variant	NM_004169.5(SHMT1):c.925A>G (p.Ile309Val)	not specified [RCV004325374]	uncertain significance	17	18335565	18335565	Human		name
404993559	CV2851007	single nucleotide variant	NM_004169.5(SHMT1):c.773C>T (p.Thr258Ile)	not provided [RCV003491478]\|not specified [RCV004364893]	uncertain significance	17	18340084	18340084	Human		name
405732363	CV3314600	single nucleotide variant	NM_004169.5(SHMT1):c.315G>C (p.Lys105Asn)	not specified [RCV004451185]	uncertain significance	17	18348368	18348368	Human		name
405732372	CV3314601	single nucleotide variant	NM_004169.5(SHMT1):c.322C>T (p.Pro108Ser)	not specified [RCV004451186]	uncertain significance	17	18348361	18348361	Human		name
405732382	CV3314602	single nucleotide variant	NM_004169.5(SHMT1):c.572G>A (p.Arg191His)	not specified [RCV004451187]	uncertain significance	17	18340761	18340761	Human		name
405732391	CV3314603	single nucleotide variant	NM_004169.5(SHMT1):c.665G>A (p.Gly222Glu)	not specified [RCV004451188]	uncertain significance	17	18340192	18340192	Human		name
405732394	CV3314604	single nucleotide variant	NM_004169.5(SHMT1):c.700G>A (p.Gly234Arg)	not specified [RCV004451189]	uncertain significance	17	18340157	18340157	Human		name
405732406	CV3314605	single nucleotide variant	NM_004169.5(SHMT1):c.710C>T (p.Ala237Val)	not specified [RCV004451190]	likely benign	17	18340147	18340147	Human		name
405732413	CV3314606	single nucleotide variant	NM_004169.5(SHMT1):c.788G>A (p.Arg263Gln)	not specified [RCV004451191]	uncertain significance	17	18340069	18340069	Human		name
405732424	CV3314607	single nucleotide variant	NM_004169.5(SHMT1):c.896G>T (p.Gly299Val)	not specified [RCV004451192]	uncertain significance	17	18335594	18335594	Human		name
407519188	CV3480549	single nucleotide variant	NM_004169.5(SHMT1):c.468C>G (p.Asp156Glu)	not specified [RCV004676381]	uncertain significance	17	18347547	18347547	Human		name
597718584	CV3602681	single nucleotide variant	NM_004169.5(SHMT1):c.958A>G (p.Met320Val)	not specified [RCV004861777]	uncertain significance	17	18333262	18333262	Human		name
597718595	CV3602682	single nucleotide variant	NM_004169.5(SHMT1):c.616T>C (p.Ser206Pro)	not specified [RCV004861778]	uncertain significance	17	18340241	18340241	Human		name
597718614	CV3602684	single nucleotide variant	NM_004169.5(SHMT1):c.394G>C (p.Val132Leu)	not specified [RCV004861780]	uncertain significance	17	18347621	18347621	Human		name
597718625	CV3602685	single nucleotide variant	NM_004169.5(SHMT1):c.508A>G (p.Met170Val)	not specified [RCV004861781]	uncertain significance	17	18347507	18347507	Human		name
597718654	CV3602688	single nucleotide variant	NM_004169.5(SHMT1):c.850A>G (p.Ile284Val)	not specified [RCV004861784]	uncertain significance	17	18335640	18335640	Human		name
597718665	CV3602689	single nucleotide variant	NM_004169.5(SHMT1):c.643C>T (p.Arg215Trp)	not specified [RCV004861785]	uncertain significance	17	18340214	18340214	Human		name
598242038	CV3914243	single nucleotide variant	NM_004169.5(SHMT1):c.806A>G (p.Tyr269Cys)	not specified [RCV005276452]	uncertain significance	17	18340051	18340051	Human		name
598199264	CV3914244	single nucleotide variant	NM_004169.5(SHMT1):c.646A>G (p.Lys216Glu)	not specified [RCV005268369]	uncertain significance	17	18340211	18340211	Human		name
598242054	CV3914247	single nucleotide variant	NM_004169.5(SHMT1):c.620G>A (p.Arg207Gln)	not specified [RCV005276455]	uncertain significance	17	18340237	18340237	Human		name
15200784	CV704009	single nucleotide variant	NM_004169.5(SHMT1):c.647A>G (p.Lys216Arg)	not provided [RCV000957429]	benign	17	18340210	18340210	Human		name
15194341	CV755699	single nucleotide variant	NM_004169.5(SHMT1):c.637C>T (p.Arg213Trp)	not provided [RCV000911097]	likely benign	17	18340220	18340220	Human		name
9684487	CV167454	single nucleotide variant	NM_004169.5(SHMT1):c.1420C>T (p.Leu474Phe)	Gastrointestinal stromal tumor [RCV000144920]	uncertain significance	17	18328782	18328782	Human	2	name
156236338	CV2224115	single nucleotide variant	NM_004169.5(SHMT1):c.1376C>T (p.Ala459Val)	not specified [RCV004095978]	uncertain significance	17	18328826	18328826	Human		name
156224080	CV2229707	single nucleotide variant	NM_004169.5(SHMT1):c.1421T>G (p.Leu474Arg)	not specified [RCV004103511]	uncertain significance	17	18328781	18328781	Human		name
156094368	CV2310007	single nucleotide variant	NM_004169.5(SHMT1):c.1046T>C (p.Ile349Thr)	not specified [RCV004163148]	uncertain significance	17	18333174	18333174	Human		name
156305610	CV2314667	single nucleotide variant	NM_004169.5(SHMT1):c.1135G>T (p.Ala379Ser)	not specified [RCV004170819]	uncertain significance	17	18330591	18330591	Human		name
156205764	CV2385246	single nucleotide variant	NM_004169.5(SHMT1):c.1030G>C (p.Glu344Gln)	not specified [RCV004228490]	uncertain significance	17	18333190	18333190	Human		name
329378375	CV2446986	single nucleotide variant	NM_004169.5(SHMT1):c.1316C>T (p.Thr439Ile)	not specified [RCV004257825]	likely benign	17	18328886	18328886	Human		name
401874224	CV2773701	single nucleotide variant	NM_004169.5(SHMT1):c.1433C>G (p.Pro478Arg)	not specified [RCV004356382]	uncertain significance	17	18328769	18328769	Human		name
405732338	CV3314596	single nucleotide variant	NM_004169.5(SHMT1):c.1189C>T (p.Arg397Trp)	not specified [RCV004451181]	uncertain significance	17	18329371	18329371	Human		name
405732344	CV3314597	single nucleotide variant	NM_004169.5(SHMT1):c.1204C>T (p.Arg402Trp)	not specified [RCV004451182]	uncertain significance	17	18329356	18329356	Human		name
405732353	CV3314598	single nucleotide variant	NM_004169.5(SHMT1):c.1341G>T (p.Glu447Asp)	not specified [RCV004451183]	uncertain significance	17	18328861	18328861	Human		name
407501267	CV3480548	single nucleotide variant	NM_004169.5(SHMT1):c.1231C>T (p.Arg411Cys)	not specified [RCV004669694]	uncertain significance	17	18329329	18329329	Human		name
597718645	CV3602687	single nucleotide variant	NM_004169.5(SHMT1):c.1063G>C (p.Asp355His)	not specified [RCV004861783]	uncertain significance	17	18330663	18330663	Human		name
598242033	CV3914242	single nucleotide variant	NM_004169.5(SHMT1):c.1248A>T (p.Lys416Asn)	not specified [RCV005276451]	uncertain significance	17	18329312	18329312	Human		name
15196501	CV727047	single nucleotide variant	NM_004169.5(SHMT1):c.1018G>C (p.Glu340Gln)	not provided [RCV000889792]	benign	17	18333202	18333202	Human		name

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