Vash2 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

31 records found for search term Vash2

Refine Term:

Sort By:

Export

CSV

TAB

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

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message