Vgll2 Variant Search Result - Rat Genome Database

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37 records found for search term Vgll2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15170845	CV699270	single nucleotide variant	NM_182645.3(VGLL2):c.99C>A (p.Ser33=)	not provided [RCV000949725]	benign	6	117268199	117268199	Human		name
156072626	CV2201353	single nucleotide variant	NM_182645.3(VGLL2):c.85C>G (p.Leu29Val)	not specified [RCV004077478]	uncertain significance	6	117268185	117268185	Human		name
401723086	CV2674705	single nucleotide variant	NM_182645.3(VGLL2):c.151G>A (p.Gly51Ser)	not specified [RCV004293993]	uncertain significance	6	117268251	117268251	Human		name
405806839	CV3345620	single nucleotide variant	NM_182645.3(VGLL2):c.250C>T (p.Arg84Cys)	not specified [RCV004480407]	uncertain significance	6	117268350	117268350	Human		name
405806841	CV3345621	single nucleotide variant	NM_182645.3(VGLL2):c.292G>C (p.Val98Leu)	not specified [RCV004480408]	uncertain significance	6	117268392	117268392	Human		name
597803881	CV3629613	single nucleotide variant	NM_182645.3(VGLL2):c.221G>T (p.Arg74Leu)	not specified [RCV004881994]	uncertain significance	6	117268321	117268321	Human		name
597803883	CV3629614	single nucleotide variant	NM_182645.3(VGLL2):c.220C>T (p.Arg74Cys)	not specified [RCV004881995]	uncertain significance	6	117268320	117268320	Human		name
598240672	CV3929589	single nucleotide variant	NM_182645.3(VGLL2):c.150C>A (p.Ser50Arg)	not specified [RCV005296803]	uncertain significance	6	117268250	117268250	Human		name
155989443	CV2282732	single nucleotide variant	NM_182645.3(VGLL2):c.647C>G (p.Ala216Gly)	not specified [RCV004141593]	uncertain significance	6	117270798	117270798	Human		name
156062447	CV2351414	single nucleotide variant	NM_182645.3(VGLL2):c.872C>T (p.Ser291Leu)	not specified [RCV004193102]	uncertain significance	6	117271023	117271023	Human		name
156346319	CV2382730	single nucleotide variant	NM_182645.3(VGLL2):c.551G>A (p.Gly184Asp)	not specified [RCV004224080]	uncertain significance	6	117270702	117270702	Human		name
156221308	CV2392437	single nucleotide variant	NM_182645.3(VGLL2):c.817G>A (p.Gly273Ser)	not specified [RCV004244016]	uncertain significance	6	117270968	117270968	Human		name
329383597	CV2425038	single nucleotide variant	NM_182645.3(VGLL2):c.594C>G (p.His198Gln)	not specified [RCV004250694]	uncertain significance	6	117270745	117270745	Human		name
405806843	CV3345622	single nucleotide variant	NM_182645.3(VGLL2):c.301G>A (p.Glu101Lys)	not specified [RCV004480409]	uncertain significance	6	117268401	117268401	Human		name
405806845	CV3345623	single nucleotide variant	NM_182645.3(VGLL2):c.421T>G (p.Phe141Val)	not specified [RCV004480410]	uncertain significance	6	117270572	117270572	Human		name
405806847	CV3345624	single nucleotide variant	NM_182645.3(VGLL2):c.509C>T (p.Pro170Leu)	not specified [RCV004480411]	uncertain significance	6	117270660	117270660	Human		name
405806849	CV3345625	single nucleotide variant	NM_182645.3(VGLL2):c.694G>C (p.Ala232Pro)	not specified [RCV004480412]	uncertain significance	6	117270845	117270845	Human		name
405806851	CV3345626	single nucleotide variant	NM_182645.3(VGLL2):c.739G>A (p.Ala247Thr)	not specified [RCV004480413]	uncertain significance	6	117270890	117270890	Human		name
405806853	CV3345627	single nucleotide variant	NM_182645.3(VGLL2):c.757C>G (p.Arg253Gly)	not specified [RCV004480414]	uncertain significance	6	117270908	117270908	Human		name
405806855	CV3345628	single nucleotide variant	NM_182645.3(VGLL2):c.769G>T (p.Ala257Ser)	not specified [RCV004480415]	uncertain significance	6	117270920	117270920	Human		name
405806858	CV3345629	single nucleotide variant	NM_182645.3(VGLL2):c.866G>T (p.Ser289Ile)	not specified [RCV004480416]	uncertain significance	6	117271017	117271017	Human		name
405806860	CV3345630	single nucleotide variant	NM_182645.3(VGLL2):c.887A>G (p.Gln296Arg)	not specified [RCV004480417]	uncertain significance	6	117271038	117271038	Human		name
407529622	CV3493480	single nucleotide variant	NM_182645.3(VGLL2):c.609C>G (p.His203Gln)	not specified [RCV004681008]	uncertain significance	6	117270760	117270760	Human		name
407529624	CV3493481	single nucleotide variant	NM_182645.3(VGLL2):c.608A>G (p.His203Arg)	not specified [RCV004681009]	uncertain significance	6	117270759	117270759	Human		name
407529626	CV3493482	single nucleotide variant	NM_182645.3(VGLL2):c.698C>G (p.Pro233Arg)	not specified [RCV004681010]	uncertain significance	6	117270849	117270849	Human		name
407529628	CV3493483	single nucleotide variant	NM_182645.3(VGLL2):c.357C>A (p.Ser119Arg)	not specified [RCV004681011]	uncertain significance	6	117268457	117268457	Human		name
597803879	CV3629612	single nucleotide variant	NM_182645.3(VGLL2):c.824C>G (p.Pro275Arg)	not specified [RCV004881993]	uncertain significance	6	117270975	117270975	Human		name
597698576	CV3629615	single nucleotide variant	NM_182645.3(VGLL2):c.609C>A (p.His203Gln)	not specified [RCV004885393]	uncertain significance	6	117270760	117270760	Human		name
597803885	CV3629616	single nucleotide variant	NM_182645.3(VGLL2):c.325C>G (p.Gln109Glu)	not specified [RCV004881996]	uncertain significance	6	117268425	117268425	Human		name
597803887	CV3629617	single nucleotide variant	NM_182645.3(VGLL2):c.353C>A (p.Thr118Asn)	not specified [RCV004881997]	uncertain significance	6	117268453	117268453	Human		name
598240680	CV3929590	single nucleotide variant	NM_182645.3(VGLL2):c.638C>T (p.Ala213Val)	not specified [RCV005296804]	uncertain significance	6	117270789	117270789	Human		name
598205970	CV3929591	single nucleotide variant	NM_182645.3(VGLL2):c.631G>A (p.Gly211Ser)	not specified [RCV005290937]	uncertain significance	6	117270782	117270782	Human		name
598240687	CV3929592	single nucleotide variant	NM_182645.3(VGLL2):c.380G>C (p.Gly127Ala)	not specified [RCV005296805]	uncertain significance	6	117268480	117268480	Human		name
598240694	CV3929593	single nucleotide variant	NM_182645.3(VGLL2):c.861C>G (p.Phe287Leu)	not specified [RCV005296806]	uncertain significance	6	117271012	117271012	Human		name
598205985	CV3929595	single nucleotide variant	NM_182645.3(VGLL2):c.523G>A (p.Asp175Asn)	not specified [RCV005290939]	uncertain significance	6	117270674	117270674	Human		name
15110384	CV710134	single nucleotide variant	NM_182645.3(VGLL2):c.382C>G (p.Pro128Ala)	not provided [RCV000960888]	benign	6	117268482	117268482	Human		name
15175826	CV735378	single nucleotide variant	NM_182645.3(VGLL2):c.467C>A (p.Pro156Gln)	not provided [RCV000906300]	benign	6	117270618	117270618	Human		name

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