Mreg Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

22 records found for search term Mreg

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597662244	CV3560870	single nucleotide variant	NM_018000.3(MREG):c.13G>A (p.Asp5Asn)	not specified [RCV004828609]	uncertain significance	2	216013315	216013315	Human		name
329355535	CV2445529	single nucleotide variant	NM_018000.3(MREG):c.31T>C (p.Cys11Arg)	not specified [RCV004257581]	uncertain significance	2	216013297	216013297	Human		name
598168822	CV3982664	single nucleotide variant	NM_018000.3(MREG):c.85C>T (p.Pro29Ser)	not specified [RCV005369773]	uncertain significance	2	216013243	216013243	Human		name
156375003	CV2195006	single nucleotide variant	NM_018000.3(MREG):c.229C>T (p.Arg77Cys)	not specified [RCV004077569]	uncertain significance	2	215996332	215996332	Human		name
155918124	CV2362506	single nucleotide variant	NM_018000.3(MREG):c.184A>G (p.Thr62Ala)	not specified [RCV004213126]	uncertain significance	2	215996377	215996377	Human		name
401899680	CV2764986	single nucleotide variant	NM_018000.3(MREG):c.212A>G (p.Tyr71Cys)	not specified [RCV004337111]	uncertain significance	2	215996349	215996349	Human		name
405750275	CV3370359	single nucleotide variant	NM_018000.3(MREG):c.209T>C (p.Leu70Pro)	not specified [RCV004499024]	uncertain significance	2	215996352	215996352	Human		name
405750340	CV3370367	single nucleotide variant	NM_018000.3(MREG):c.245A>G (p.Lys82Arg)	not specified [RCV004499032]	uncertain significance	2	215996316	215996316	Human		name
405751154	CV3370370	single nucleotide variant	NM_018000.3(MREG):c.293G>A (p.Arg98Gln)	not specified [RCV004499035]	uncertain significance	2	215947076	215947076	Human		name
407496628	CV3450170	single nucleotide variant	NM_018000.3(MREG):c.223G>A (p.Val75Ile)	not specified [RCV004643541]	uncertain significance	2	215996338	215996338	Human		name
408367691	CV3511033	single nucleotide variant	NM_018000.3(MREG):c.113C>T (p.Ser38Phe)	MREG-related condition [RCV004759057]	likely benign	2	215996448	215996448	Human		name , trait
598168816	CV3982663	single nucleotide variant	NM_018000.3(MREG):c.230G>A (p.Arg77His)	not specified [RCV005369772]	uncertain significance	2	215996331	215996331	Human		name
155947759	CV2262777	single nucleotide variant	NM_018000.3(MREG):c.514C>T (p.Arg172Cys)	not specified [RCV004130948]	uncertain significance	2	215944994	215944994	Human		name
156075356	CV2281514	single nucleotide variant	NM_018000.3(MREG):c.314G>C (p.Arg105Thr)	not specified [RCV004153826]	uncertain significance	2	215947055	215947055	Human		name
329380221	CV2444266	single nucleotide variant	NM_018000.3(MREG):c.546C>G (p.Phe182Leu)	not specified [RCV004263034]	uncertain significance	2	215944962	215944962	Human		name
401718945	CV2679359	single nucleotide variant	NM_018000.3(MREG):c.493A>G (p.Arg165Gly)	not specified [RCV004285894]	uncertain significance	2	215945588	215945588	Human		name
401736249	CV2689295	single nucleotide variant	NM_018000.3(MREG):c.563G>A (p.Arg188Gln)	not specified [RCV004306128]	likely benign	2	215944945	215944945	Human		name
401740234	CV2705925	single nucleotide variant	NM_018000.3(MREG):c.419G>A (p.Arg140Lys)	not specified [RCV004320853]	uncertain significance	2	215945662	215945662	Human		name
401893099	CV2762870	single nucleotide variant	NM_018000.3(MREG):c.416C>A (p.Thr139Lys)	not specified [RCV004340414]	uncertain significance	2	215945665	215945665	Human		name
405751103	CV3370377	single nucleotide variant	NM_018000.3(MREG):c.371T>C (p.Leu124Ser)	not specified [RCV004499042]	uncertain significance	2	215945710	215945710	Human		name
597637558	CV3560869	single nucleotide variant	NM_018000.3(MREG):c.560G>A (p.Arg187His)	not specified [RCV004824749]	uncertain significance	2	215944948	215944948	Human		name
598202008	CV3982662	single nucleotide variant	NM_018000.3(MREG):c.425C>T (p.Ala142Val)	not specified [RCV005376154]	uncertain significance	2	215945656	215945656	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