Tarbp2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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28 records found for search term Tarbp2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15118972	CV779674	single nucleotide variant	NM_134323.2(TARBP2):c.423-3C>G	not provided [RCV000962472]	benign	12	53504394	53504394	Human		name
401857804	CV2759913	single nucleotide variant	NM_134323.2(TARBP2):c.25G>A (p.Gly9Ser)	not specified [RCV004345339]	uncertain significance	12	53501433	53501433	Human		name
156055194	CV2361355	single nucleotide variant	NM_134323.2(TARBP2):c.52A>G (p.Ser18Gly)	not specified [RCV004218558]	uncertain significance	12	53501460	53501460	Human		name
155904795	CV2385603	single nucleotide variant	NM_134323.2(TARBP2):c.47T>C (p.Leu16Pro)	not specified [RCV004233238]	uncertain significance	12	53501455	53501455	Human		name
405764231	CV3327916	single nucleotide variant	NM_134323.2(TARBP2):c.44G>A (p.Gly15Glu)	not specified [RCV004469160]	uncertain significance	12	53501452	53501452	Human		name
407451164	CV3475237	single nucleotide variant	NM_134323.2(TARBP2):c.37G>A (p.Gly13Ser)	not specified [RCV004673217]	uncertain significance	12	53501445	53501445	Human		name
597687873	CV3612418	single nucleotide variant	NM_134323.2(TARBP2):c.40T>A (p.Cys14Ser)	not specified [RCV004866442]	uncertain significance	12	53501448	53501448	Human		name
597687883	CV3612420	single nucleotide variant	NM_134323.2(TARBP2):c.42C>G (p.Cys14Trp)	not specified [RCV004866444]	uncertain significance	12	53501450	53501450	Human		name
15199549	CV702394	single nucleotide variant	NM_134323.2(TARBP2):c.942T>C (p.Ile314=)	not provided [RCV000957070]	benign	12	53505849	53505849	Human		name
401749172	CV2692979	single nucleotide variant	NM_134323.2(TARBP2):c.269T>A (p.Val90Glu)	not specified [RCV004306492]	uncertain significance	12	53503072	53503072	Human		name
407511749	CV3475234	single nucleotide variant	NM_134323.2(TARBP2):c.215G>A (p.Ser72Asn)	not specified [RCV004673214]	uncertain significance	12	53502176	53502176	Human		name
156257927	CV2264915	single nucleotide variant	NM_134323.2(TARBP2):c.977T>C (p.Leu326Pro)	not specified [RCV004134660]	uncertain significance	12	53506024	53506024	Human		name
329374770	CV2440021	single nucleotide variant	NM_134323.2(TARBP2):c.298A>G (p.Met100Val)	not specified [RCV004260495]	uncertain significance	12	53503101	53503101	Human		name
329381435	CV2471132	single nucleotide variant	NM_134323.2(TARBP2):c.520C>T (p.Arg174Trp)	not specified [RCV004278385]	uncertain significance	12	53504722	53504722	Human		name
401891757	CV2780732	single nucleotide variant	NM_134323.2(TARBP2):c.983A>T (p.Glu328Val)	not specified [RCV004352065]	uncertain significance	12	53506030	53506030	Human		name
405764236	CV3327917	single nucleotide variant	NM_134323.2(TARBP2):c.599G>A (p.Arg200His)	not specified [RCV004469161]	uncertain significance	12	53504801	53504801	Human		name
405764243	CV3327918	single nucleotide variant	NM_134323.2(TARBP2):c.886C>T (p.Arg296Cys)	not specified [RCV004469162]	uncertain significance	12	53505793	53505793	Human		name
405764247	CV3327919	single nucleotide variant	NM_134323.2(TARBP2):c.998C>T (p.Pro333Leu)	not specified [RCV004469163]	uncertain significance	12	53506045	53506045	Human		name
407511751	CV3475235	single nucleotide variant	NM_134323.2(TARBP2):c.430C>T (p.Pro144Ser)	not specified [RCV004673215]	uncertain significance	12	53504404	53504404	Human		name
407511755	CV3475236	single nucleotide variant	NM_134323.2(TARBP2):c.515G>C (p.Gly172Ala)	not specified [RCV004673216]	uncertain significance	12	53504717	53504717	Human		name
597749356	CV3612419	single nucleotide variant	NM_134323.2(TARBP2):c.367C>G (p.Pro123Ala)	not specified [RCV004866443]	uncertain significance	12	53503753	53503753	Human		name
597749373	CV3612423	single nucleotide variant	NM_134323.2(TARBP2):c.839G>T (p.Arg280Leu)	not specified [RCV004866447]	uncertain significance	12	53505746	53505746	Human		name
598194574	CV3920166	single nucleotide variant	NM_134323.2(TARBP2):c.345C>G (p.Asp115Glu)	not specified [RCV005289095]	uncertain significance	12	53503731	53503731	Human		name
156268189	CV2305737	single nucleotide variant	NM_134323.2(TARBP2):c.1050G>C (p.Glu350Asp)	not specified [RCV004167553]	uncertain significance	12	53506097	53506097	Human		name
401768617	CV2735366	single nucleotide variant	NM_134323.2(TARBP2):c.1000G>A (p.Ala334Thr)	not specified [RCV004334021]	uncertain significance	12	53506047	53506047	Human		name
405764226	CV3327915	single nucleotide variant	NM_134323.2(TARBP2):c.1057C>T (p.Arg353Cys)	not specified [RCV004469159]	uncertain significance	12	53506104	53506104	Human		name
597749362	CV3612421	single nucleotide variant	NM_134323.2(TARBP2):c.1060C>T (p.Arg354Cys)	not specified [RCV004866445]	uncertain significance	12	53506107	53506107	Human		name
597749367	CV3612422	single nucleotide variant	NM_134323.2(TARBP2):c.1045G>A (p.Gly349Ser)	not specified [RCV004866446]	uncertain significance	12	53506092	53506092	Human		name

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