Armc8 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

33 records found for search term Armc8

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155972358	CV2228164	single nucleotide variant	NM_001363941.2(ARMC8):c.274A>G (p.Met92Val)	not specified [RCV004096376]	uncertain significance	3	138223468	138223468	Human		name
598165488	CV3908724	single nucleotide variant	NM_001363941.2(ARMC8):c.123A>G (p.Ile41Met)	not specified [RCV005261879]	uncertain significance	3	138221926	138221926	Human		name
156003978	CV2254242	single nucleotide variant	NM_001363941.2(ARMC8):c.330A>C (p.Leu110Phe)	not specified [RCV004129918]	uncertain significance	3	138223524	138223524	Human		name
155965197	CV2286892	single nucleotide variant	NM_001363941.2(ARMC8):c.356T>C (p.Leu119Pro)	not specified [RCV004144506]	uncertain significance	3	138223654	138223654	Human		name
155953377	CV2303023	single nucleotide variant	NM_001363941.2(ARMC8):c.811A>G (p.Thr271Ala)	not specified [RCV004156815]	uncertain significance	3	138239502	138239502	Human		name
156040312	CV2310791	single nucleotide variant	NM_001363941.2(ARMC8):c.363T>A (p.Phe121Leu)	not specified [RCV004157716]	uncertain significance	3	138223661	138223661	Human		name
156200311	CV2313064	single nucleotide variant	NM_001363941.2(ARMC8):c.877T>G (p.Leu293Val)	not specified [RCV004161340]	uncertain significance	3	138241822	138241822	Human		name
156204411	CV2314143	single nucleotide variant	NM_001363941.2(ARMC8):c.917A>G (p.Tyr306Cys)	not specified [RCV004166229]	uncertain significance	3	138241862	138241862	Human		name
156087960	CV2337831	single nucleotide variant	NM_001363941.2(ARMC8):c.886G>C (p.Glu296Gln)	not specified [RCV004183842]	uncertain significance	3	138241831	138241831	Human		name
329387665	CV2470879	single nucleotide variant	NM_001363941.2(ARMC8):c.659C>T (p.Pro220Leu)	not specified [RCV004276081]	uncertain significance	3	138237358	138237358	Human		name
401770854	CV2686047	single nucleotide variant	NM_001363941.2(ARMC8):c.809G>A (p.Arg270Gln)	not specified [RCV004297060]	uncertain significance	3	138239500	138239500	Human		name
401860213	CV2768517	single nucleotide variant	NM_001363941.2(ARMC8):c.482G>A (p.Arg161His)	not specified [RCV004344397]	uncertain significance	3	138228964	138228964	Human		name
401895843	CV2768940	single nucleotide variant	NM_001363941.2(ARMC8):c.395T>C (p.Ile132Thr)	not specified [RCV004347038]	uncertain significance	3	138223693	138223693	Human		name
405663372	CV3290246	single nucleotide variant	NM_001363941.2(ARMC8):c.322C>G (p.Pro108Ala)	not specified [RCV004418019]	uncertain significance	3	138223516	138223516	Human		name
405663379	CV3290247	single nucleotide variant	NM_001363941.2(ARMC8):c.808C>T (p.Arg270Trp)	not specified [RCV004418020]	uncertain significance	3	138239499	138239499	Human		name
405663384	CV3290248	single nucleotide variant	NM_001363941.2(ARMC8):c.929C>G (p.Pro310Arg)	not specified [RCV004418021]	uncertain significance	3	138241874	138241874	Human		name
407468534	CV3473141	single nucleotide variant	NM_001363941.2(ARMC8):c.593C>T (p.Thr198Ile)	not specified [RCV004661151]	uncertain significance	3	138235098	138235098	Human		name
597708056	CV3589680	single nucleotide variant	NM_001363941.2(ARMC8):c.745C>T (p.Pro249Ser)	not specified [RCV004860681]	uncertain significance	3	138237541	138237541	Human		name
598165522	CV3908730	single nucleotide variant	NM_001363941.2(ARMC8):c.812C>G (p.Thr271Arg)	not specified [RCV005261885]	uncertain significance	3	138239503	138239503	Human		name
598165596	CV3908744	single nucleotide variant	NM_001363941.2(ARMC8):c.934G>T (p.Val312Phe)	not specified [RCV005261899]	uncertain significance	3	138241879	138241879	Human		name
151350311	CV1322337	single nucleotide variant	NM_001363941.2(ARMC8):c.1998G>C (p.Met666Ile)	not provided [RCV001806961]	uncertain significance	3	138295868	138295868	Human		name
156365631	CV2272146	single nucleotide variant	NM_001363941.2(ARMC8):c.1996A>G (p.Met666Val)	not specified [RCV004124924]	uncertain significance	3	138295866	138295866	Human		name
155974474	CV2341437	single nucleotide variant	NM_001363941.2(ARMC8):c.1408G>A (p.Val470Ile)	not specified [RCV004188834]	uncertain significance	3	138270061	138270061	Human		name
405663360	CV3290243	single nucleotide variant	NM_001363941.2(ARMC8):c.1126C>T (p.Arg376Trp)	not specified [RCV004418016]	uncertain significance	3	138245175	138245175	Human		name
405663363	CV3290244	single nucleotide variant	NM_001363941.2(ARMC8):c.1528A>G (p.Ser510Gly)	not specified [RCV004418017]	uncertain significance	3	138273015	138273015	Human		name
405663367	CV3290245	single nucleotide variant	NM_001363941.2(ARMC8):c.1648A>G (p.Ser550Gly)	not specified [RCV004418018]	uncertain significance	3	138274467	138274467	Human		name
407451263	CV3473150	single nucleotide variant	NM_001363941.2(ARMC8):c.1735A>C (p.Ile579Leu)	not specified [RCV004674362]	uncertain significance	3	138284440	138284440	Human		name
597686567	CV3589673	single nucleotide variant	NM_001363941.2(ARMC8):c.1678G>A (p.Val560Ile)	not specified [RCV004854550]	uncertain significance	3	138274497	138274497	Human		name
597686577	CV3589690	single nucleotide variant	NM_001363941.2(ARMC8):c.1881G>C (p.Trp627Cys)	not specified [RCV004854561]	uncertain significance	3	138289107	138289107	Human		name
597687132	CV3589701	single nucleotide variant	NM_001363941.2(ARMC8):c.1624C>T (p.Arg542Cys)	not specified [RCV004860691]	uncertain significance	3	138273111	138273111	Human		name
597687471	CV3589712	single nucleotide variant	NM_001363941.2(ARMC8):c.1862G>A (p.Cys621Tyr)	not specified [RCV004860697]	uncertain significance	3	138289088	138289088	Human		name
598165482	CV3908723	single nucleotide variant	NM_001363941.2(ARMC8):c.1688T>C (p.Ile563Thr)	not specified [RCV005261878]	uncertain significance	3	138274507	138274507	Human		name
598165549	CV3908735	single nucleotide variant	NM_001363941.2(ARMC8):c.1654C>T (p.His552Tyr)	not specified [RCV005261890]	uncertain significance	3	138274473	138274473	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