Ptgs1 Variant Search Result - Rat Genome Database

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59 records found for search term Ptgs1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
11087737	CV227768	single nucleotide variant	NM_000962.3(PTGS1):c.-842A>G	aspirin response - Efficacy [RCV000211226]	drug response	9	122370243	122370243	Human		name
15184895	CV779571	single nucleotide variant	NM_000962.4(PTGS1):c.762+10G>A	not provided [RCV000975223]	benign	9	122381757	122381757	Human		name
150449959	CV1232617	single nucleotide variant	NM_000962.4(PTGS1):c.123G>A (p.Gln41=)	not provided [RCV001647692]	benign	9	122377927	122377927	Human		name
15153991	CV711746	single nucleotide variant	NM_000962.4(PTGS1):c.204C>T (p.Cys68=)	PTGS1-related disorder [RCV003905954]\|not provided [RCV000968651]	benign	9	122378008	122378008	Human		name , trait , alternate_id
401911130	CV2826374	single nucleotide variant	NM_000962.4(PTGS1):c.786G>A (p.Pro262=)	not provided [RCV003425779]	likely benign	9	122383532	122383532	Human		name
401918437	CV2826375	single nucleotide variant	NM_000962.4(PTGS1):c.960C>G (p.Pro320=)	not provided [RCV003430235]	likely benign	9	122383706	122383706	Human		name
407491336	CV3468311	single nucleotide variant	NM_000962.4(PTGS1):c.61G>A (p.Val21Ile)	not specified [RCV004666870]	uncertain significance	9	122371239	122371239	Human		name
15099832	CV767081	single nucleotide variant	NM_000962.4(PTGS1):c.906G>A (p.Thr302=)	not provided [RCV000936541]	likely benign	9	122383652	122383652	Human		name
156225249	CV2399604	single nucleotide variant	NM_000962.4(PTGS1):c.179G>A (p.Arg60His)	not specified [RCV004244123]	uncertain significance	9	122377983	122377983	Human		name
405673578	CV3377864	single nucleotide variant	NM_000962.4(PTGS1):c.245G>A (p.Arg82Gln)	not specified [RCV004515724]	uncertain significance	9	122378466	122378466	Human		name
407491332	CV3468310	single nucleotide variant	NM_000962.4(PTGS1):c.291G>T (p.Trp97Cys)	not specified [RCV004666869]	uncertain significance	9	122378512	122378512	Human		name
596932450	CV3539070	single nucleotide variant	NM_000962.4(PTGS1):c.211C>T (p.Pro71Ser)	not provided [RCV004793196]	uncertain significance	9	122378015	122378015	Human		name
598180838	CV3904694	single nucleotide variant	NM_000962.4(PTGS1):c.182C>T (p.Thr61Met)	not specified [RCV005265089]	uncertain significance	9	122377986	122377986	Human		name
598180844	CV3904695	single nucleotide variant	NM_000962.4(PTGS1):c.113A>T (p.Tyr38Phe)	not specified [RCV005265090]	uncertain significance	9	122377917	122377917	Human		name
15193557	CV700783	single nucleotide variant	NM_000962.4(PTGS1):c.1497G>A (p.Ala499=)	not provided [RCV000955405]	benign	9	122392241	122392241	Human		name
15195894	CV767082	single nucleotide variant	NM_000962.4(PTGS1):c.1098C>T (p.Phe366=)	not provided [RCV000934067]	likely benign	9	122386534	122386534	Human		name
8633221	CV88434	single nucleotide variant	NM_000962.3(PTGS1):c.1587C>T (p.Ser529=)	Malignant melanoma [RCV000068526]	not provided	9	122392331	122392331	Human		name
156197332	CV2259258	single nucleotide variant	NM_000962.4(PTGS1):c.731G>A (p.Arg244Gln)	not specified [RCV004122278]	uncertain significance	9	122381716	122381716	Human		name
156253550	CV2325536	single nucleotide variant	NM_000962.4(PTGS1):c.532C>T (p.Arg178Cys)	not specified [RCV004179973]	uncertain significance	9	122381406	122381406	Human		name
156353404	CV2327531	single nucleotide variant	NM_000962.4(PTGS1):c.716G>A (p.Arg239His)	not specified [RCV004176837]	uncertain significance	9	122381701	122381701	Human		name
155972587	CV2335816	single nucleotide variant	NM_000962.4(PTGS1):c.730C>T (p.Arg244Trp)	not specified [RCV004196051]	uncertain significance	9	122381715	122381715	Human		name
156209046	CV2382576	single nucleotide variant	NM_000962.4(PTGS1):c.989C>T (p.Thr330Met)	not specified [RCV004232904]	uncertain significance	9	122383735	122383735	Human		name
401734407	CV2723334	single nucleotide variant	NM_000962.4(PTGS1):c.719A>C (p.Gln240Pro)	Hemorrhage [RCV003313823]\|not specified [RCV004329552]	uncertain significance	9	122381704	122381704	Human	1	name
401721484	CV2737598	single nucleotide variant	NM_000962.4(PTGS1):c.412T>C (p.Trp138Arg)	Hemorrhage [RCV003314539]	uncertain significance	9	122378834	122378834	Human	1	name
401871645	CV2759961	single nucleotide variant	NM_000962.4(PTGS1):c.821A>G (p.Tyr274Cys)	not specified [RCV004345383]	uncertain significance	9	122383567	122383567	Human		name
401872766	CV2779999	single nucleotide variant	NM_000962.4(PTGS1):c.769G>T (p.Asp257Tyr)	not specified [RCV004353586]	uncertain significance	9	122383515	122383515	Human		name
401894639	CV2785068	single nucleotide variant	NM_000962.4(PTGS1):c.568C>A (p.Pro190Thr)	not specified [RCV004355084]	uncertain significance	9	122381442	122381442	Human		name
405008977	CV2853151	single nucleotide variant	NM_000962.4(PTGS1):c.994C>T (p.Arg332Cys)	not specified [RCV003494345]	uncertain significance	9	122383740	122383740	Human		name
405673582	CV3377865	single nucleotide variant	NM_000962.4(PTGS1):c.707A>G (p.Asn236Ser)	not specified [RCV004515725]	uncertain significance	9	122381692	122381692	Human		name
405673585	CV3377866	single nucleotide variant	NM_000962.4(PTGS1):c.928C>G (p.Arg310Gly)	not specified [RCV004515726]	uncertain significance	9	122383674	122383674	Human		name
598172882	CV3904693	single nucleotide variant	NM_000962.4(PTGS1):c.742G>T (p.Asp248Tyr)	not specified [RCV005263608]	uncertain significance	9	122381727	122381727	Human		name
598180851	CV3904696	single nucleotide variant	NM_000962.4(PTGS1):c.597C>A (p.Phe199Leu)	not specified [RCV005265091]	uncertain significance	9	122381471	122381471	Human		name
598180858	CV3904697	single nucleotide variant	NM_000962.4(PTGS1):c.484A>G (p.Met162Val)	not specified [RCV005265092]	uncertain significance	9	122378906	122378906	Human		name
598180863	CV3904698	single nucleotide variant	NM_000962.4(PTGS1):c.359C>G (p.Ser120Cys)	not specified [RCV005265093]	uncertain significance	9	122378781	122378781	Human		name
155987209	CV2234076	single nucleotide variant	NM_000962.4(PTGS1):c.1169T>C (p.Met390Thr)	not specified [RCV004106182]	uncertain significance	9	122386605	122386605	Human		name
156088084	CV2337861	single nucleotide variant	NM_000962.4(PTGS1):c.1396C>A (p.Arg466Ser)	not specified [RCV004183871]	uncertain significance	9	122390297	122390297	Human		name
156135140	CV2347195	single nucleotide variant	NM_000962.4(PTGS1):c.1654G>A (p.Glu552Lys)	not specified [RCV004204666]	uncertain significance	9	122392398	122392398	Human		name
156268398	CV2372029	single nucleotide variant	NM_000962.4(PTGS1):c.1118G>A (p.Arg373His)	not specified [RCV004221701]	uncertain significance	9	122386554	122386554	Human		name
156073633	CV2376915	single nucleotide variant	NM_000962.4(PTGS1):c.1699G>A (p.Val567Ile)	not specified [RCV004229605]	uncertain significance	9	122392443	122392443	Human		name
401734758	CV2737079	single nucleotide variant	NM_000962.4(PTGS1):c.1571T>C (p.Ile524Thr)	Hemorrhage [RCV003313871]	uncertain significance	9	122392315	122392315	Human	1	name
401857398	CV2759153	single nucleotide variant	NM_000962.4(PTGS1):c.1729G>A (p.Val577Ile)	not specified [RCV004342449]	uncertain significance	9	122392473	122392473	Human		name
401892435	CV2781947	single nucleotide variant	NM_000962.4(PTGS1):c.1777G>A (p.Glu593Lys)	not specified [RCV004357183]	uncertain significance	9	122392521	122392521	Human		name
401892381	CV2785360	single nucleotide variant	NM_000962.4(PTGS1):c.1739G>A (p.Arg580His)	not specified [RCV004357109]	likely benign	9	122392483	122392483	Human		name
405264211	CV3185198	single nucleotide variant	NM_000962.4(PTGS1):c.1441G>A (p.Val481Ile)	not provided [RCV003885762]	likely benign	9	122390342	122390342	Human		name
405291579	CV3205875	single nucleotide variant	NM_000962.4(PTGS1):c.1342G>A (p.Val448Met)	PTGS1-related disorder [RCV003963993]	likely benign	9	122390243	122390243	Human		name , trait , alternate_id
405673551	CV3377858	single nucleotide variant	NM_000962.4(PTGS1):c.1178C>A (p.Ser393Tyr)	not specified [RCV004515718]	uncertain significance	9	122386614	122386614	Human		name
405673556	CV3377859	single nucleotide variant	NM_000962.4(PTGS1):c.1198G>C (p.Glu400Gln)	not specified [RCV004515719]	uncertain significance	9	122386634	122386634	Human		name
405673561	CV3377860	single nucleotide variant	NM_000962.4(PTGS1):c.1295G>A (p.Arg432Gln)	not specified [RCV004515720]	uncertain significance	9	122386731	122386731	Human		name
405673565	CV3377861	single nucleotide variant	NM_000962.4(PTGS1):c.1372C>T (p.Arg458Trp)	not specified [RCV004515721]	uncertain significance	9	122390273	122390273	Human		name
405673576	CV3377863	single nucleotide variant	NM_000962.4(PTGS1):c.1753A>G (p.Ser585Gly)	not specified [RCV004515723]	uncertain significance	9	122392497	122392497	Human		name
597781492	CV3588781	single nucleotide variant	NM_000962.4(PTGS1):c.1716G>T (p.Lys572Asn)	not specified [RCV004853754]	uncertain significance	9	122392460	122392460	Human		name
597781499	CV3588783	single nucleotide variant	NM_000962.4(PTGS1):c.1789A>G (p.Thr597Ala)	not specified [RCV004853756]	uncertain significance	9	122392533	122392533	Human		name
597781505	CV3588784	single nucleotide variant	NM_000962.4(PTGS1):c.1396C>T (p.Arg466Cys)	not specified [RCV004853757]	uncertain significance	9	122390297	122390297	Human		name
597781509	CV3588785	single nucleotide variant	NM_000962.4(PTGS1):c.1603G>A (p.Gly535Arg)	not specified [RCV004853758]	uncertain significance	9	122392347	122392347	Human		name
597781513	CV3588786	single nucleotide variant	NM_000962.4(PTGS1):c.1525G>C (p.Glu509Gln)	not specified [RCV004853759]	uncertain significance	9	122392269	122392269	Human		name
598180871	CV3904699	single nucleotide variant	NM_000962.4(PTGS1):c.1781G>A (p.Arg594Gln)	not specified [RCV005265094]	uncertain significance	9	122392525	122392525	Human		name
8626659	CV81803	single nucleotide variant	NM_000962.3(PTGS1):c.1610C>T (p.Pro537Leu)	Malignant melanoma [RCV000061881]	not provided	9	122392354	122392354	Human		name
8633222	CV88435	single nucleotide variant	NM_000962.3(PTGS1):c.1733C>T (p.Ser578Phe)	Malignant melanoma [RCV000068527]	not provided	9	122392477	122392477	Human		name
15165318	CV723314	microsatellite	NM_000962.4(PTGS1):c.38TGCTCC[1] (p.Leu15_Leu16del)	not provided [RCV000882385]	likely benign	9	122371213	122371218	Human		name

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