Rundc3b Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

36 records found for search term Rundc3b

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8649522	CV126096	single nucleotide variant	NM_001134405.1(RUNDC3B):c.630-4676C>A	Lung cancer [RCV000106583]	uncertain significance	7	87765905	87765905	Human		name
405700758	CV3309959	single nucleotide variant	NM_001134405.2(RUNDC3B):c.239-6464A>T	not specified [RCV004447037]	uncertain significance	7	87693957	87693957	Human		name
598233437	CV3910003	single nucleotide variant	NM_001134405.2(RUNDC3B):c.5C>T (p.Ala2Val)	not specified [RCV005274867]	uncertain significance	7	87628828	87628828	Human		name
155985756	CV2233919	single nucleotide variant	NM_001134405.2(RUNDC3B):c.40G>A (p.Gly14Ser)	not specified [RCV004104272]	uncertain significance	7	87628863	87628863	Human		name
156347479	CV2315304	single nucleotide variant	NM_001134405.2(RUNDC3B):c.38G>C (p.Arg13Pro)	not specified [RCV004167289]	uncertain significance	7	87628861	87628861	Human		name
155906648	CV2379086	single nucleotide variant	NM_001134405.2(RUNDC3B):c.43G>A (p.Gly15Ser)	not specified [RCV004233840]	uncertain significance	7	87628866	87628866	Human		name
597687323	CV3597581	single nucleotide variant	NM_001134405.2(RUNDC3B):c.79C>G (p.Arg27Gly)	not specified [RCV004863306]	uncertain significance	7	87628902	87628902	Human		name
597687331	CV3597585	single nucleotide variant	NM_001134405.2(RUNDC3B):c.98G>A (p.Arg33Lys)	not specified [RCV004863310]	uncertain significance	7	87628921	87628921	Human		name
598233423	CV3910001	single nucleotide variant	NM_001134405.2(RUNDC3B):c.85G>A (p.Ala29Thr)	not specified [RCV005274865]	uncertain significance	7	87628908	87628908	Human		name
598233430	CV3910002	single nucleotide variant	NM_001134405.2(RUNDC3B):c.36C>G (p.Ile12Met)	not specified [RCV005274866]	uncertain significance	7	87628859	87628859	Human		name
8626471	CV81615	single nucleotide variant	NM_001134405.1(RUNDC3B):c.459G>A (p.Arg153=)	Malignant melanoma [RCV000061693]	not provided	7	87739791	87739791	Human		name
329349891	CV2454645	single nucleotide variant	NM_001134405.2(RUNDC3B):c.271C>T (p.Arg91Cys)	not specified [RCV004268104]	uncertain significance	7	87700453	87700453	Human		name
329349908	CV2460043	single nucleotide variant	NM_001134405.2(RUNDC3B):c.218T>G (p.Ile73Ser)	not specified [RCV004273168]	uncertain significance	7	87650917	87650917	Human		name
407450561	CV3473204	single nucleotide variant	NM_001134405.2(RUNDC3B):c.265A>T (p.Ser89Cys)	not specified [RCV004661194]	uncertain significance	7	87700447	87700447	Human		name
597687339	CV3597586	single nucleotide variant	NM_001134405.2(RUNDC3B):c.205A>G (p.Ile69Val)	not specified [RCV004863311]	uncertain significance	7	87650904	87650904	Human		name
8632677	CV87892	single nucleotide variant	NM_001134405.1(RUNDC3B):c.262G>A (p.Glu88Lys)	Malignant melanoma [RCV000067984]	not provided	7	87700444	87700444	Human		name
155931043	CV2220964	single nucleotide variant	NM_001134405.2(RUNDC3B):c.455C>A (p.Thr152Asn)	not specified [RCV004092651]	uncertain significance	7	87710652	87710652	Human		name
156346498	CV2300594	single nucleotide variant	NM_001134405.2(RUNDC3B):c.305G>A (p.Arg102Gln)	not specified [RCV004155555]	uncertain significance	7	87700487	87700487	Human		name
156188634	CV2328662	single nucleotide variant	NM_001134405.2(RUNDC3B):c.329G>A (p.Cys110Tyr)	not specified [RCV004177905]	uncertain significance	7	87700511	87700511	Human		name
401727878	CV2678543	single nucleotide variant	NM_001134405.2(RUNDC3B):c.892G>A (p.Asp298Asn)	not specified [RCV004292553]	uncertain significance	7	87777891	87777891	Human		name
401736139	CV2703053	single nucleotide variant	NM_001134405.2(RUNDC3B):c.774G>C (p.Lys258Asn)	not specified [RCV004321357]	uncertain significance	7	87770725	87770725	Human		name
401749509	CV2719864	single nucleotide variant	NM_001134405.2(RUNDC3B):c.378A>T (p.Arg126Ser)	not specified [RCV004329277]	uncertain significance	7	87710575	87710575	Human		name
401894220	CV2770446	single nucleotide variant	NM_001134405.2(RUNDC3B):c.989G>A (p.Arg330Lys)	not specified [RCV004358085]	uncertain significance	7	87807405	87807405	Human		name
401881966	CV2784021	single nucleotide variant	NM_001134405.2(RUNDC3B):c.713G>T (p.Gly238Val)	not specified [RCV004362428]	uncertain significance	7	87770664	87770664	Human		name
405700767	CV3309960	single nucleotide variant	NM_001134405.2(RUNDC3B):c.770A>T (p.Gln257Leu)	not specified [RCV004447038]	uncertain significance	7	87770721	87770721	Human		name
407468664	CV3473202	single nucleotide variant	NM_001134405.2(RUNDC3B):c.931A>G (p.Ile311Val)	not specified [RCV004661193]	uncertain significance	7	87777930	87777930	Human		name
407514123	CV3473203	single nucleotide variant	NM_001134405.2(RUNDC3B):c.901C>A (p.His301Asn)	not specified [RCV004674380]	uncertain significance	7	87777900	87777900	Human		name
597733312	CV3597583	single nucleotide variant	NM_001134405.2(RUNDC3B):c.485T>C (p.Val162Ala)	not specified [RCV004863308]	uncertain significance	7	87739817	87739817	Human		name
156322388	CV2205032	single nucleotide variant	NM_001134405.2(RUNDC3B):c.1084C>G (p.His362Asp)	not specified [RCV004077647]	uncertain significance	7	87807500	87807500	Human		name
156173045	CV2317082	single nucleotide variant	NM_001134405.2(RUNDC3B):c.1010T>C (p.Leu337Pro)	not specified [RCV004174566]	uncertain significance	7	87807426	87807426	Human		name
156199384	CV2362865	single nucleotide variant	NM_001134405.2(RUNDC3B):c.1144A>G (p.Ser382Gly)	not specified [RCV004208974]	uncertain significance	7	87816181	87816181	Human		name
329395347	CV2458288	single nucleotide variant	NM_001134405.2(RUNDC3B):c.1190A>T (p.Asp397Val)	not specified [RCV004265935]	uncertain significance	7	87816227	87816227	Human		name
401870954	CV2759351	single nucleotide variant	NM_001134405.2(RUNDC3B):c.1298C>G (p.Thr433Arg)	not specified [RCV004335934]	uncertain significance	7	87829957	87829957	Human		name
401893818	CV2759852	single nucleotide variant	NM_001134405.2(RUNDC3B):c.1156A>G (p.Thr386Ala)	not specified [RCV004345286]	uncertain significance	7	87816193	87816193	Human		name
401890696	CV2772123	single nucleotide variant	NM_001134405.2(RUNDC3B):c.1120C>T (p.Leu374Phe)	not specified [RCV004344774]	uncertain significance	7	87816157	87816157	Human		name
597733300	CV3597582	single nucleotide variant	NM_001134405.2(RUNDC3B):c.1037C>T (p.Ala346Val)	not specified [RCV004863307]	uncertain significance	7	87807453	87807453	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