Tarm1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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27 records found for search term Tarm1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156194036	CV2398155	single nucleotide variant	NM_001135686.3(TARM1):c.86C>T (p.Pro29Leu)	not specified [RCV004241731]	uncertain significance	19	54075099	54075099	Human		name
401778966	CV2733020	single nucleotide variant	NM_001135686.3(TARM1):c.43G>A (p.Val15Met)	not specified [RCV004331192]	likely benign	19	54075910	54075910	Human		name
405764261	CV3327921	single nucleotide variant	NM_001135686.3(TARM1):c.28T>C (p.Cys10Arg)	not specified [RCV004469165]	uncertain significance	19	54081313	54081313	Human		name
597794786	CV3612427	single nucleotide variant	NM_001135686.3(TARM1):c.89C>T (p.Ser30Phe)	not specified [RCV004877971]	uncertain significance	19	54075096	54075096	Human		name
598264985	CV3920170	single nucleotide variant	NM_001135686.3(TARM1):c.94A>C (p.Ser32Arg)	not specified [RCV005280884]	uncertain significance	19	54075091	54075091	Human		name
155987751	CV2251149	single nucleotide variant	NM_001135686.3(TARM1):c.143G>A (p.Arg48Gln)	not specified [RCV004115385]	uncertain significance	19	54075042	54075042	Human		name
156099595	CV2367405	single nucleotide variant	NM_001135686.3(TARM1):c.152C>T (p.Thr51Ile)	not specified [RCV004209306]	uncertain significance	19	54075033	54075033	Human		name
155917704	CV2199080	single nucleotide variant	NM_001135686.3(TARM1):c.494C>T (p.Thr165Met)	not specified [RCV004080480]	uncertain significance	19	54074084	54074084	Human		name
156038633	CV2214992	single nucleotide variant	NM_001135686.3(TARM1):c.524C>T (p.Ala175Val)	not specified [RCV004084769]	uncertain significance	19	54074054	54074054	Human		name
156272811	CV2277599	single nucleotide variant	NM_001135686.3(TARM1):c.575G>C (p.Gly192Ala)	not specified [RCV004147068]	uncertain significance	19	54074003	54074003	Human		name
155975387	CV2327772	single nucleotide variant	NM_001135686.3(TARM1):c.670A>G (p.Thr224Ala)	not specified [RCV004179118]	uncertain significance	19	54070149	54070149	Human		name
156402151	CV2368078	single nucleotide variant	NM_001135686.3(TARM1):c.556G>A (p.Val186Met)	not specified [RCV004216431]	uncertain significance	19	54074022	54074022	Human		name
156049733	CV2391109	single nucleotide variant	NM_001135686.3(TARM1):c.709C>G (p.Leu237Val)	not specified [RCV004235091]	uncertain significance	19	54070110	54070110	Human		name
156006848	CV2394258	single nucleotide variant	NM_001135686.3(TARM1):c.502C>T (p.Pro168Ser)	not specified [RCV004238491]	uncertain significance	19	54074076	54074076	Human		name
329395290	CV2457900	single nucleotide variant	NM_001135686.3(TARM1):c.619G>A (p.Ala207Thr)	not specified [RCV004271491]	uncertain significance	19	54073959	54073959	Human		name
401742318	CV2677558	single nucleotide variant	NM_001135686.3(TARM1):c.446G>A (p.Arg149Gln)	not specified [RCV004291662]	uncertain significance	19	54074132	54074132	Human		name
401899271	CV2783799	single nucleotide variant	NM_001135686.3(TARM1):c.596A>G (p.Tyr199Cys)	not specified [RCV004360711]	uncertain significance	19	54073982	54073982	Human		name
405764268	CV3327922	single nucleotide variant	NM_001135686.3(TARM1):c.413C>T (p.Ala138Val)	not specified [RCV004469166]	uncertain significance	19	54074165	54074165	Human		name
405764272	CV3327923	single nucleotide variant	NM_001135686.3(TARM1):c.659T>C (p.Val220Ala)	not specified [RCV004469167]	uncertain significance	19	54070160	54070160	Human		name
405764279	CV3327924	single nucleotide variant	NM_001135686.3(TARM1):c.676T>C (p.Ser226Pro)	not specified [RCV004469168]	uncertain significance	19	54070143	54070143	Human		name
405764285	CV3327925	single nucleotide variant	NM_001135686.3(TARM1):c.760G>A (p.Ala254Thr)	not specified [RCV004469169]	uncertain significance	19	54070059	54070059	Human		name
597749378	CV3612428	single nucleotide variant	NM_001135686.3(TARM1):c.422G>T (p.Arg141Met)	not specified [RCV004866448]	uncertain significance	19	54074156	54074156	Human		name
598194580	CV3920167	single nucleotide variant	NM_001135686.3(TARM1):c.316C>T (p.His106Tyr)	not specified [RCV005289096]	uncertain significance	19	54074869	54074869	Human		name
598194587	CV3920169	single nucleotide variant	NM_001135686.3(TARM1):c.568G>A (p.Asp190Asn)	not specified [RCV005289097]	uncertain significance	19	54074010	54074010	Human		name
598194594	CV3920171	single nucleotide variant	NM_001135686.3(TARM1):c.628C>G (p.Pro210Ala)	not specified [RCV005289098]	uncertain significance	19	54073950	54073950	Human		name
598194601	CV3920172	single nucleotide variant	NM_001135686.3(TARM1):c.740T>G (p.Met247Arg)	not specified [RCV005289099]	uncertain significance	19	54070079	54070079	Human		name
598194609	CV3920173	single nucleotide variant	NM_001135686.3(TARM1):c.335G>A (p.Ser112Asn)	not specified [RCV005289100]	uncertain significance	19	54074850	54074850	Human		name

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