Gpr137c Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

32 records found for search term Gpr137c

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405716725	CV3255140	single nucleotide variant	NM_001099652.2(GPR137C):c.7G>A (p.Val3Met)	not specified [RCV004388288]	uncertain significance	14	52553154	52553154	Human		name
156166409	CV2398928	single nucleotide variant	NM_001099652.2(GPR137C):c.20G>C (p.Gly7Ala)	not specified [RCV004245242]	uncertain significance	14	52553167	52553167	Human		name
405716704	CV3255137	single nucleotide variant	NM_001099652.2(GPR137C):c.26C>T (p.Ala9Val)	not specified [RCV004388285]	uncertain significance	14	52553173	52553173	Human		name
155976128	CV2211350	single nucleotide variant	NM_001099652.2(GPR137C):c.56A>C (p.Glu19Ala)	not specified [RCV004090272]	uncertain significance	14	52553203	52553203	Human		name
155923168	CV2215486	single nucleotide variant	NM_001099652.2(GPR137C):c.58C>G (p.Pro20Ala)	not specified [RCV004089276]	uncertain significance	14	52553205	52553205	Human		name
155932356	CV2232064	single nucleotide variant	NM_001099652.2(GPR137C):c.41C>T (p.Pro14Leu)	not specified [RCV004093108]	uncertain significance	14	52553188	52553188	Human		name
597744545	CV3684737	single nucleotide variant	NM_001099652.2(GPR137C):c.43G>T (p.Ala15Ser)	not specified [RCV004922279]	uncertain significance	14	52553190	52553190	Human		name
597744548	CV3684738	single nucleotide variant	NM_001099652.2(GPR137C):c.28G>A (p.Ala10Thr)	not specified [RCV004922280]	uncertain significance	14	52553175	52553175	Human		name
598233618	CV3971010	single nucleotide variant	NM_001099652.2(GPR137C):c.52C>A (p.Arg18Ser)	not specified [RCV005342788]	uncertain significance	14	52553199	52553199	Human		name
156339628	CV2271443	single nucleotide variant	NM_001099652.2(GPR137C):c.185C>G (p.Ala62Gly)	not specified [RCV004136546]	uncertain significance	14	52553332	52553332	Human		name
156043321	CV2387967	single nucleotide variant	NM_001099652.2(GPR137C):c.217C>G (p.Leu73Val)	not specified [RCV004236505]	uncertain significance	14	52553364	52553364	Human		name
401767700	CV2681748	single nucleotide variant	NM_001099652.2(GPR137C):c.125C>T (p.Pro42Leu)	not specified [RCV004294289]	uncertain significance	14	52553272	52553272	Human		name
597790056	CV3684742	single nucleotide variant	NM_001099652.2(GPR137C):c.137A>G (p.Gln46Arg)	not specified [RCV004933019]	uncertain significance	14	52553284	52553284	Human		name
598274166	CV3971007	single nucleotide variant	NM_001099652.2(GPR137C):c.142G>T (p.Ala48Ser)	not specified [RCV005351285]	uncertain significance	14	52553289	52553289	Human		name
155973215	CV2224571	single nucleotide variant	NM_001099652.2(GPR137C):c.400C>T (p.Leu134Phe)	not specified [RCV004098145]	uncertain significance	14	52553547	52553547	Human		name
156148363	CV2394485	single nucleotide variant	NM_001099652.2(GPR137C):c.451T>C (p.Cys151Arg)	not specified [RCV004240847]	uncertain significance	14	52598278	52598278	Human		name
401748875	CV2706190	single nucleotide variant	NM_001099652.2(GPR137C):c.442G>A (p.Glu148Lys)	not specified [RCV004314868]	uncertain significance	14	52553589	52553589	Human		name
401870990	CV2756553	single nucleotide variant	NM_001099652.2(GPR137C):c.448A>T (p.Ile150Leu)	not specified [RCV004345080]	uncertain significance	14	52598275	52598275	Human		name
401856518	CV2764837	single nucleotide variant	NM_001099652.2(GPR137C):c.553G>T (p.Ala185Ser)	not specified [RCV004334935]	uncertain significance	14	52600177	52600177	Human		name
405716713	CV3255138	single nucleotide variant	NM_001099652.2(GPR137C):c.359A>G (p.His120Arg)	not specified [RCV004388286]	uncertain significance	14	52553506	52553506	Human		name
405716719	CV3255139	single nucleotide variant	NM_001099652.2(GPR137C):c.413C>T (p.Thr138Met)	not specified [RCV004388287]	uncertain significance	14	52553560	52553560	Human		name
597790060	CV3684740	single nucleotide variant	NM_001099652.2(GPR137C):c.440C>T (p.Ala147Val)	not specified [RCV004933018]	uncertain significance	14	52553587	52553587	Human		name
597744558	CV3684741	single nucleotide variant	NM_001099652.2(GPR137C):c.976A>G (p.Arg326Gly)	not specified [RCV004922282]	uncertain significance	14	52633638	52633638	Human		name
597744562	CV3684743	single nucleotide variant	NM_001099652.2(GPR137C):c.850G>A (p.Asp284Asn)	not specified [RCV004922283]	uncertain significance	14	52632292	52632292	Human		name
598274162	CV3971005	single nucleotide variant	NM_001099652.2(GPR137C):c.997C>A (p.Pro333Thr)	not specified [RCV005351283]	uncertain significance	14	52633831	52633831	Human		name
598274164	CV3971006	single nucleotide variant	NM_001099652.2(GPR137C):c.368C>T (p.Pro123Leu)	not specified [RCV005351284]	uncertain significance	14	52553515	52553515	Human		name
598274168	CV3971008	single nucleotide variant	NM_001099652.2(GPR137C):c.655T>G (p.Leu219Val)	not specified [RCV005351286]	uncertain significance	14	52600279	52600279	Human		name
598274169	CV3971009	single nucleotide variant	NM_001099652.2(GPR137C):c.505G>C (p.Gly169Arg)	not specified [RCV005351287]	uncertain significance	14	52600129	52600129	Human		name
156317478	CV2203990	single nucleotide variant	NM_001099652.2(GPR137C):c.1280C>A (p.Pro427Gln)	not specified [RCV004070031]	uncertain significance	14	52635105	52635105	Human		name
156061935	CV2392055	single nucleotide variant	NM_001099652.2(GPR137C):c.1166G>A (p.Ser389Asn)	not specified [RCV004237951]	uncertain significance	14	52634991	52634991	Human		name
405717669	CV3255135	single nucleotide variant	NM_001099652.2(GPR137C):c.1172G>A (p.Ser391Asn)	not specified [RCV004388283]	uncertain significance	14	52634997	52634997	Human		name
597744553	CV3684739	single nucleotide variant	NM_001099652.2(GPR137C):c.1048G>A (p.Asp350Asn)	not specified [RCV004922281]	uncertain significance	14	52633882	52633882	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