Ptgdr Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

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

87 records found for search term Ptgdr

Refine Term:

Assembly:

Chr

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8558672	CV20444	variation	PTGDR, HAPLOTYPE TCT	Asthma-related traits, susceptibility to, 1 [RCV000005736]	risk factor				Human		name
8558673	CV20445	variation	PTGDR, HAPLOTYPE CCC	Asthma-related traits, susceptibility to, 1 [RCV000005737]	risk factor				Human		name
598124331	CV3883422	variation	PTGDR, HAPLOTYPE CCC	Asthma-related traits, susceptibility to, 1 [RCV005235800]	risk factor				Human		name
405672987	CV3377713	single nucleotide variant	NM_000953.3(PTGDR):c.17A>T (p.Tyr6Phe)	not specified [RCV004515573]	uncertain significance	14	52267831	52267831	Human		name
597751371	CV3588668	single nucleotide variant	NM_000953.3(PTGDR):c.11C>T (p.Pro4Leu)	not specified [RCV004846642]	uncertain significance	14	52267825	52267825	Human		name
15177809	CV714160	single nucleotide variant	NM_000953.3(PTGDR):c.19C>T (p.Arg7Cys)	not provided [RCV000973516]	benign	14	52267833	52267833	Human		name
156357541	CV2318319	single nucleotide variant	NM_000953.3(PTGDR):c.32C>T (p.Thr11Ile)	not specified [RCV004179486]	uncertain significance	14	52267846	52267846	Human		name
155981824	CV2208539	single nucleotide variant	NM_000953.3(PTGDR):c.290C>T (p.Ala97Val)	not specified [RCV004091069]	likely benign	14	52268104	52268104	Human		name
156384902	CV2371641	single nucleotide variant	NM_000953.3(PTGDR):c.187A>G (p.Met63Val)	not specified [RCV004216882]	likely benign	14	52268001	52268001	Human		name
401764137	CV2725450	single nucleotide variant	NM_000953.3(PTGDR):c.154C>T (p.Arg52Cys)	not specified [RCV004320084]	uncertain significance	14	52267968	52267968	Human		name
405672990	CV3377714	single nucleotide variant	NM_000953.3(PTGDR):c.283G>A (p.Val95Met)	not specified [RCV004515574]	uncertain significance	14	52268097	52268097	Human		name
407491435	CV3468258	single nucleotide variant	NM_000953.3(PTGDR):c.107T>C (p.Leu36Pro)	not specified [RCV004666853]	uncertain significance	14	52267921	52267921	Human		name
597751367	CV3588667	single nucleotide variant	NM_000953.3(PTGDR):c.176C>T (p.Ser59Leu)	not specified [RCV004846641]	uncertain significance	14	52267990	52267990	Human		name
597751381	CV3588670	single nucleotide variant	NM_000953.3(PTGDR):c.295G>T (p.Ala99Ser)	not specified [RCV004846644]	uncertain significance	14	52268109	52268109	Human		name
598172365	CV3908508	single nucleotide variant	NM_000953.3(PTGDR):c.281G>C (p.Arg94Pro)	not specified [RCV005263536]	uncertain significance	14	52268095	52268095	Human		name
598172372	CV3908510	single nucleotide variant	NM_000953.3(PTGDR):c.101A>G (p.Asn34Ser)	not specified [RCV005263537]	uncertain significance	14	52267915	52267915	Human		name
126914046	CV1038284	single nucleotide variant	NM_000953.3(PTGDR):c.928C>T (p.Arg310Ter)	not provided [RCV001357921]	uncertain significance	14	52274812	52274812	Human		name
156034991	CV2208028	single nucleotide variant	NM_000953.3(PTGDR):c.740G>A (p.Arg247His)	not specified [RCV004086727]	uncertain significance	14	52268554	52268554	Human		name
156001237	CV2257832	single nucleotide variant	NM_000953.3(PTGDR):c.873G>T (p.Lys291Asn)	not specified [RCV004127881]	uncertain significance	14	52274757	52274757	Human		name
156069579	CV2355854	single nucleotide variant	NM_000953.3(PTGDR):c.743C>T (p.Ala248Val)	not specified [RCV004201250]	uncertain significance	14	52268557	52268557	Human		name
329351946	CV2455516	single nucleotide variant	NM_000953.3(PTGDR):c.484G>A (p.Ala162Thr)	not specified [RCV004276779]	uncertain significance	14	52268298	52268298	Human		name
401729815	CV2683806	single nucleotide variant	NM_000953.3(PTGDR):c.514G>A (p.Gly172Arg)	not specified [RCV004284535]	uncertain significance	14	52268328	52268328	Human		name
401742734	CV2697851	single nucleotide variant	NM_000953.3(PTGDR):c.796C>A (p.Leu266Met)	not specified [RCV004300564]	uncertain significance	14	52268610	52268610	Human		name
401759815	CV2701733	single nucleotide variant	NM_000953.3(PTGDR):c.710G>A (p.Arg237His)	not specified [RCV004314138]	uncertain significance	14	52268524	52268524	Human		name
401863654	CV2777060	single nucleotide variant	NM_000953.3(PTGDR):c.988G>C (p.Val330Leu)	not specified [RCV004351851]	uncertain significance	14	52274872	52274872	Human		name
401902014	CV2810423	single nucleotide variant	NM_000953.3(PTGDR):c.995G>A (p.Arg332Gln)	not provided [RCV003393432]	likely benign	14	52274879	52274879	Human		name
405699208	CV3227084	single nucleotide variant	NM_000953.3(PTGDR):c.828G>A (p.Met276Ile)	not provided [RCV003993478]	uncertain significance	14	52268642	52268642	Human		name
405672994	CV3377715	single nucleotide variant	NM_000953.3(PTGDR):c.571G>A (p.Glu191Lys)	not specified [RCV004515575]	uncertain significance	14	52268385	52268385	Human		name
405672999	CV3377716	single nucleotide variant	NM_000953.3(PTGDR):c.596A>T (p.Tyr199Phe)	not specified [RCV004515576]	uncertain significance	14	52268410	52268410	Human		name
405673002	CV3377717	single nucleotide variant	NM_000953.3(PTGDR):c.808A>G (p.Met270Val)	not specified [RCV004515577]	uncertain significance	14	52268622	52268622	Human		name
407425085	CV3409344	single nucleotide variant	NM_000953.3(PTGDR):c.758C>G (p.Ala253Gly)	not provided [RCV004585275]	likely benign	14	52268572	52268572	Human		name
407491341	CV3468259	single nucleotide variant	NM_000953.3(PTGDR):c.803C>A (p.Ala268Glu)	not specified [RCV004666854]	uncertain significance	14	52268617	52268617	Human		name
407491267	CV3468260	single nucleotide variant	NM_000953.3(PTGDR):c.904G>A (p.Glu302Lys)	not specified [RCV004666855]	uncertain significance	14	52274788	52274788	Human		name
407532063	CV3468261	single nucleotide variant	NM_000953.3(PTGDR):c.610T>C (p.Ser204Pro)	not specified [RCV004657949]	uncertain significance	14	52268424	52268424	Human		name
597751362	CV3588666	single nucleotide variant	NM_000953.3(PTGDR):c.584C>T (p.Ser195Leu)	not specified [RCV004846640]	uncertain significance	14	52268398	52268398	Human		name
597751376	CV3588669	single nucleotide variant	NM_000953.3(PTGDR):c.721A>G (p.Arg241Gly)	not specified [RCV004846643]	uncertain significance	14	52268535	52268535	Human		name
598172357	CV3908507	single nucleotide variant	NM_000953.3(PTGDR):c.686A>G (p.His229Arg)	not specified [RCV005263535]	uncertain significance	14	52268500	52268500	Human		name
598203212	CV3908509	single nucleotide variant	NM_000953.3(PTGDR):c.511T>G (p.Phe171Val)	not specified [RCV005269338]	uncertain significance	14	52268325	52268325	Human		name
598172378	CV3908511	single nucleotide variant	NM_000953.3(PTGDR):c.994C>T (p.Arg332Trp)	not specified [RCV005263538]	uncertain significance	14	52274878	52274878	Human		name
598172387	CV3908512	single nucleotide variant	NM_000953.3(PTGDR):c.410C>T (p.Pro137Leu)	not specified [RCV005263539]	uncertain significance	14	52268224	52268224	Human		name
598172394	CV3908513	single nucleotide variant	NM_000953.3(PTGDR):c.561G>A (p.Met187Ile)	not specified [RCV005263540]	uncertain significance	14	52268375	52268375	Human		name
8627536	CV82680	single nucleotide variant	NM_000953.2(PTGDR):c.568G>A (p.Glu190Lys)	Malignant melanoma [RCV000062760]	not provided	14	52268382	52268382	Human		name
156316852	CV2193115	single nucleotide variant	NM_000953.3(PTGDR):c.1055C>T (p.Ser352Phe)	not specified [RCV004071119]	uncertain significance	14	52274939	52274939	Human		name
401730088	CV2700421	single nucleotide variant	NM_000953.3(PTGDR):c.1063A>G (p.Met355Val)	not specified [RCV004311066]	likely benign	14	52274947	52274947	Human		name
401877291	CV2769403	single nucleotide variant	NM_000953.3(PTGDR):c.1064T>C (p.Met355Thr)	not specified [RCV004357390]	uncertain significance	14	52274948	52274948	Human		name
405672982	CV3377712	single nucleotide variant	NM_000953.3(PTGDR):c.1072A>T (p.Ser358Cys)	not specified [RCV004515572]	uncertain significance	14	52274956	52274956	Human		name
597751391	CV3588672	single nucleotide variant	NM_000953.3(PTGDR):c.1018A>T (p.Ile340Phe)	not specified [RCV004846646]	uncertain significance	14	52274902	52274902	Human		name
156381054	CV2219113	single nucleotide variant	NM_004778.3(PTGDR2):c.41T>C (p.Leu14Pro)	not specified [RCV004087271]	uncertain significance	11	60853682	60853682	Human		name
597751699	CV3588674	single nucleotide variant	NM_004778.3(PTGDR2):c.56G>C (p.Arg19Pro)	not specified [RCV004846648]	uncertain significance	11	60853667	60853667	Human		name
401756713	CV2696449	single nucleotide variant	NM_004778.3(PTGDR2):c.154G>C (p.Val52Leu)	not specified [RCV004312528]	likely benign	11	60853569	60853569	Human		name
401756715	CV2696450	single nucleotide variant	NM_004778.3(PTGDR2):c.241T>A (p.Ser81Thr)	not specified [RCV004312529]	likely benign	11	60853482	60853482	Human		name
598172426	CV3908517	single nucleotide variant	NM_004778.3(PTGDR2):c.166G>A (p.Val56Met)	not specified [RCV005263544]	uncertain significance	11	60853557	60853557	Human		name
156314658	CV2196675	single nucleotide variant	NM_004778.3(PTGDR2):c.851G>A (p.Arg284His)	not specified [RCV004073935]	uncertain significance	11	60852872	60852872	Human		name
156036065	CV2253276	single nucleotide variant	NM_004778.3(PTGDR2):c.922T>G (p.Cys308Gly)	not specified [RCV004122810]	uncertain significance	11	60852801	60852801	Human		name
156001249	CV2257833	single nucleotide variant	NM_004778.3(PTGDR2):c.965T>C (p.Val322Ala)	not specified [RCV004127882]	uncertain significance	11	60852758	60852758	Human		name
156148797	CV2321800	single nucleotide variant	NM_004778.3(PTGDR2):c.454T>G (p.Cys152Gly)	not specified [RCV004179788]	uncertain significance	11	60853269	60853269	Human		name
156307523	CV2332017	single nucleotide variant	NM_004778.3(PTGDR2):c.812G>A (p.Arg271Gln)	not specified [RCV004189073]	uncertain significance	11	60852911	60852911	Human		name
155920729	CV2350556	single nucleotide variant	NM_004778.3(PTGDR2):c.404G>C (p.Arg135Pro)	not specified [RCV004204910]	uncertain significance	11	60853319	60853319	Human		name
156346186	CV2377940	single nucleotide variant	NM_004778.3(PTGDR2):c.949C>T (p.Arg317Cys)	not specified [RCV004230506]	uncertain significance	11	60852774	60852774	Human		name
329369446	CV2424823	single nucleotide variant	NM_004778.3(PTGDR2):c.765C>A (p.Phe255Leu)	not specified [RCV004248711]	uncertain significance	11	60852958	60852958	Human		name
401735451	CV2672656	single nucleotide variant	NM_004778.3(PTGDR2):c.541A>G (p.Met181Val)	not specified [RCV004287677]	uncertain significance	11	60853182	60853182	Human		name
401750331	CV2701154	single nucleotide variant	NM_004778.3(PTGDR2):c.922T>C (p.Cys308Arg)	not specified [RCV004309737]	uncertain significance	11	60852801	60852801	Human		name
401750918	CV2712272	single nucleotide variant	NM_004778.3(PTGDR2):c.434T>G (p.Val145Gly)	not specified [RCV004313768]	uncertain significance	11	60853289	60853289	Human		name
401765698	CV2717819	single nucleotide variant	NM_004778.3(PTGDR2):c.824A>G (p.Asn275Ser)	not specified [RCV004321800]	uncertain significance	11	60852899	60852899	Human		name
401855536	CV2757337	single nucleotide variant	NM_004778.3(PTGDR2):c.695G>T (p.Arg232Leu)	not specified [RCV004340745]	uncertain significance	11	60853028	60853028	Human		name
401893978	CV2770180	single nucleotide variant	NM_004778.3(PTGDR2):c.740T>C (p.Leu247Pro)	not specified [RCV004356074]	uncertain significance	11	60852983	60852983	Human		name
405673007	CV3377718	single nucleotide variant	NM_004778.3(PTGDR2):c.365T>C (p.Leu122Pro)	not specified [RCV004515578]	uncertain significance	11	60853358	60853358	Human		name
405673011	CV3377719	single nucleotide variant	NM_004778.3(PTGDR2):c.404G>A (p.Arg135Gln)	not specified [RCV004515579]	uncertain significance	11	60853319	60853319	Human		name
405673015	CV3377720	single nucleotide variant	NM_004778.3(PTGDR2):c.443C>T (p.Ala148Val)	not specified [RCV004515580]	uncertain significance	11	60853280	60853280	Human		name
405673019	CV3377721	single nucleotide variant	NM_004778.3(PTGDR2):c.559C>G (p.Leu187Val)	not specified [RCV004515581]	uncertain significance	11	60853164	60853164	Human		name
405673021	CV3377722	single nucleotide variant	NM_004778.3(PTGDR2):c.628A>G (p.Lys210Glu)	not specified [RCV004515582]	uncertain significance	11	60853095	60853095	Human		name
405673025	CV3377723	single nucleotide variant	NM_004778.3(PTGDR2):c.789C>A (p.His263Gln)	not specified [RCV004515583]	uncertain significance	11	60852934	60852934	Human		name
405673028	CV3377724	single nucleotide variant	NM_004778.3(PTGDR2):c.979C>A (p.Leu327Met)	not specified [RCV004515584]	uncertain significance	11	60852744	60852744	Human		name
405673032	CV3377725	single nucleotide variant	NM_004778.3(PTGDR2):c.994G>C (p.Glu332Gln)	not specified [RCV004515585]	uncertain significance	11	60852729	60852729	Human		name
407491273	CV3468263	single nucleotide variant	NM_004778.3(PTGDR2):c.448A>C (p.Lys150Gln)	not specified [RCV004666856]	uncertain significance	11	60853275	60853275	Human		name
597751704	CV3588673	single nucleotide variant	NM_004778.3(PTGDR2):c.427C>T (p.Arg143Cys)	not specified [RCV004846647]	uncertain significance	11	60853296	60853296	Human		name
597751694	CV3588675	single nucleotide variant	NM_004778.3(PTGDR2):c.893T>C (p.Val298Ala)	not specified [RCV004846649]	uncertain significance	11	60852830	60852830	Human		name
597751686	CV3588677	single nucleotide variant	NM_004778.3(PTGDR2):c.535C>A (p.Arg179Ser)	not specified [RCV004846651]	uncertain significance	11	60853188	60853188	Human		name
598172409	CV3908515	single nucleotide variant	NM_004778.3(PTGDR2):c.544T>C (p.Cys182Arg)	not specified [RCV005263542]	uncertain significance	11	60853179	60853179	Human		name
598172418	CV3908516	single nucleotide variant	NM_004778.3(PTGDR2):c.439G>A (p.Ala147Thr)	not specified [RCV005263543]	uncertain significance	11	60853284	60853284	Human		name
15151608	CV752718	single nucleotide variant	NM_004778.3(PTGDR2):c.841C>T (p.Leu281Phe)	not provided [RCV000923710]	likely benign	11	60852882	60852882	Human		name
156371486	CV2200782	single nucleotide variant	NM_004778.3(PTGDR2):c.1086A>C (p.Glu362Asp)	not specified [RCV004081421]	uncertain significance	11	60852637	60852637	Human		name
156069169	CV2318045	single nucleotide variant	NM_004778.3(PTGDR2):c.1001G>A (p.Gly334Asp)	not specified [RCV004177148]	uncertain significance	11	60852722	60852722	Human		name
156193211	CV2344201	single nucleotide variant	NM_004778.3(PTGDR2):c.1036T>A (p.Ser346Thr)	not specified [RCV004197841]	uncertain significance	11	60852687	60852687	Human		name
401767573	CV2729767	single nucleotide variant	NM_004778.3(PTGDR2):c.1111G>C (p.Gly371Arg)	not specified [RCV004332786]	uncertain significance	11	60852612	60852612	Human		name
597751689	CV3588676	single nucleotide variant	NM_004778.3(PTGDR2):c.1076G>T (p.Arg359Leu)	not specified [RCV004846650]	uncertain significance	11	60852647	60852647	Human		name
15165927	CV712908	deletion	NM_004778.3(PTGDR2):c.449_450del (p.Lys150fs)	not provided [RCV000971057]	benign	11	60853273	60853274	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