Vash2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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31 records found for search term Vash2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156250339	CV2311213	single nucleotide variant	NM_001301056.2(VASH2):c.85C>A (p.Pro29Thr)	not specified [RCV004166300]	uncertain significance	1	212951627	212951627	Human		name
401936916	CV2816033	single nucleotide variant	NM_001301056.2(VASH2):c.717C>T (p.Tyr239=)	not provided [RCV003414759]	likely benign	1	212972799	212972799	Human		name
598240017	CV3929400	single nucleotide variant	NM_001301056.2(VASH2):c.83G>A (p.Arg28Gln)	not specified [RCV005296700]	uncertain significance	1	212951625	212951625	Human		name
401752948	CV2703545	single nucleotide variant	NM_001301056.2(VASH2):c.283A>G (p.Ile95Val)	not specified [RCV004317717]	likely benign	1	212961172	212961172	Human		name
405806263	CV3348798	single nucleotide variant	NM_001301056.2(VASH2):c.181C>T (p.His61Tyr)	not specified [RCV004480130]	uncertain significance	1	212951723	212951723	Human		name
407529385	CV3493321	single nucleotide variant	NM_001301056.2(VASH2):c.139G>C (p.Val47Leu)	not specified [RCV004680873]	uncertain significance	1	212951681	212951681	Human		name
597697789	CV3633156	single nucleotide variant	NM_001301056.2(VASH2):c.229G>A (p.Gly77Arg)	not specified [RCV004885307]	uncertain significance	1	212951771	212951771	Human		name
598240012	CV3929398	single nucleotide variant	NM_001301056.2(VASH2):c.291G>T (p.Gln97His)	not specified [RCV005296699]	uncertain significance	1	212961180	212961180	Human		name
156077164	CV2230270	single nucleotide variant	NM_001301056.2(VASH2):c.754G>A (p.Val252Ile)	not specified [RCV004099884]	uncertain significance	1	212972836	212972836	Human		name
156073228	CV2251542	single nucleotide variant	NM_001301056.2(VASH2):c.586C>G (p.Leu196Val)	not specified [RCV004117499]	uncertain significance	1	212972668	212972668	Human		name
155991556	CV2255684	single nucleotide variant	NM_001301056.2(VASH2):c.982C>T (p.Arg328Trp)	not specified [RCV004120085]	uncertain significance	1	212974057	212974057	Human		name
155977959	CV2321315	single nucleotide variant	NM_001301056.2(VASH2):c.326A>C (p.Asp109Ala)	not specified [RCV004177322]	uncertain significance	1	212961215	212961215	Human		name
155917853	CV2362433	single nucleotide variant	NM_001301056.2(VASH2):c.743T>C (p.Ile248Thr)	not specified [RCV004213054]	uncertain significance	1	212972825	212972825	Human		name
329367610	CV2456947	single nucleotide variant	NM_001301056.2(VASH2):c.925C>T (p.Arg309Trp)	not specified [RCV004270890]	uncertain significance	1	212974000	212974000	Human		name
401765076	CV2701811	single nucleotide variant	NM_001301056.2(VASH2):c.763G>A (p.Glu255Lys)	not specified [RCV004314201]	uncertain significance	1	212972845	212972845	Human		name
401765078	CV2701812	single nucleotide variant	NM_001301056.2(VASH2):c.765G>C (p.Glu255Asp)	not specified [RCV004314202]	uncertain significance	1	212972847	212972847	Human		name
401762934	CV2720134	single nucleotide variant	NM_001301056.2(VASH2):c.860C>A (p.Ala287Asp)	not specified [RCV004323695]	uncertain significance	1	212972942	212972942	Human		name
401762383	CV2723420	single nucleotide variant	NM_001301056.2(VASH2):c.685A>G (p.Ile229Val)	not specified [RCV004323495]	uncertain significance	1	212972767	212972767	Human		name
401857235	CV2762464	single nucleotide variant	NM_001301056.2(VASH2):c.574C>T (p.His192Tyr)	not specified [RCV004338001]	uncertain significance	1	212972656	212972656	Human		name
405806265	CV3348799	single nucleotide variant	NM_001301056.2(VASH2):c.338C>A (p.Ala113Glu)	not specified [RCV004480131]	uncertain significance	1	212961227	212961227	Human		name
405806267	CV3348800	single nucleotide variant	NM_001301056.2(VASH2):c.667C>T (p.Arg223Trp)	not specified [RCV004480132]	uncertain significance	1	212972749	212972749	Human		name
405806269	CV3348801	single nucleotide variant	NM_001301056.2(VASH2):c.739A>C (p.Lys247Gln)	not specified [RCV004480133]	uncertain significance	1	212972821	212972821	Human		name
405806271	CV3348802	single nucleotide variant	NM_001301056.2(VASH2):c.928G>A (p.Gly310Arg)	not specified [RCV004480134]	uncertain significance	1	212974003	212974003	Human		name
597803624	CV3633155	single nucleotide variant	NM_001301056.2(VASH2):c.686T>C (p.Ile229Thr)	not specified [RCV004881830]	uncertain significance	1	212972768	212972768	Human		name
597803626	CV3633157	single nucleotide variant	NM_001301056.2(VASH2):c.769C>T (p.His257Tyr)	not specified [RCV004881831]	uncertain significance	1	212972851	212972851	Human		name
597803629	CV3633159	single nucleotide variant	NM_001301056.2(VASH2):c.632G>T (p.Arg211Leu)	not specified [RCV004881833]	uncertain significance	1	212972714	212972714	Human		name
598205408	CV3929397	single nucleotide variant	NM_001301056.2(VASH2):c.926G>A (p.Arg309Gln)	not specified [RCV005290849]	uncertain significance	1	212974001	212974001	Human		name
598205417	CV3929399	single nucleotide variant	NM_001301056.2(VASH2):c.811G>A (p.Val271Ile)	not specified [RCV005290850]	uncertain significance	1	212972893	212972893	Human		name
598240022	CV3929401	single nucleotide variant	NM_001301056.2(VASH2):c.776T>C (p.Phe259Ser)	not specified [RCV005296701]	uncertain significance	1	212972858	212972858	Human		name
8629290	CV84435	single nucleotide variant	NM_001136474.2(VASH2):c.572C>T (p.Pro191Leu)	Malignant melanoma [RCV000064517]	not provided	1	212972849	212972849	Human		name
405806273	CV3348803	single nucleotide variant	NM_001301056.2(VASH2):c.1004T>C (p.Leu335Pro)	not specified [RCV004480135]	uncertain significance	1	212988520	212988520	Human		name

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