Parp9 Variant Search Result - Rat Genome Database

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63 records found for search term Parp9

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156329898	CV2216517	single nucleotide variant	NM_001146105.2(PARP9):c.49+10C>T	not specified [RCV004097315]	uncertain significance	3	122558424	122558424	Human		name
401753618	CV2685002	single nucleotide variant	NM_001146105.2(PARP9):c.49+27T>C	not specified [RCV004289587]	uncertain significance	3	122558407	122558407	Human		name
405773661	CV3374665	single nucleotide variant	NM_001146105.2(PARP9):c.49+15C>T	not specified [RCV004502724]	uncertain significance	3	122558419	122558419	Human		name
405773667	CV3374666	single nucleotide variant	NM_001146105.2(PARP9):c.49+21C>T	not specified [RCV004502725]	uncertain significance	3	122558413	122558413	Human		name
8625484	CV80607	single nucleotide variant	NM_001146102.1(PARP9):c.12C>T (p.Ser4=)	Malignant melanoma [RCV000060684]	not provided	3	122559609	122559609	Human		name
156044355	CV2397109	single nucleotide variant	NM_001146105.2(PARP9):c.91A>G (p.Ile31Val)	not specified [RCV004236611]	uncertain significance	3	122556080	122556080	Human		name
597670833	CV3568223	single nucleotide variant	NM_001146105.2(PARP9):c.38A>G (p.Asn13Ser)	not specified [RCV004836301]	likely benign	3	122558445	122558445	Human		name
156259667	CV2366342	single nucleotide variant	NM_001146105.2(PARP9):c.205A>T (p.Ser69Cys)	not specified [RCV004212398]	uncertain significance	3	122555966	122555966	Human		name
156071253	CV2381377	single nucleotide variant	NM_001146105.2(PARP9):c.155A>G (p.Asn52Ser)	not specified [RCV004227428]	uncertain significance	3	122556016	122556016	Human		name
329374414	CV2443894	single nucleotide variant	NM_001146105.2(PARP9):c.112A>C (p.Ile38Leu)	not specified [RCV004258227]	uncertain significance	3	122556059	122556059	Human		name
401759310	CV2708580	single nucleotide variant	NM_001146105.2(PARP9):c.211T>G (p.Ser71Ala)	not specified [RCV004307572]	uncertain significance	3	122555960	122555960	Human		name
405773636	CV3374661	single nucleotide variant	NM_001146105.2(PARP9):c.131G>A (p.Arg44His)	not specified [RCV004502720]	uncertain significance	3	122556040	122556040	Human		name
156229585	CV2199499	single nucleotide variant	NM_001146105.2(PARP9):c.674G>A (p.Arg225Gln)	not specified [RCV004071051]	uncertain significance	3	122555497	122555497	Human		name
156194934	CV2214415	single nucleotide variant	NM_001146105.2(PARP9):c.937G>T (p.Val313Leu)	not specified [RCV004088175]	uncertain significance	3	122552588	122552588	Human		name
155929752	CV2278288	single nucleotide variant	NM_001146105.2(PARP9):c.992C>T (p.Ala331Val)	not specified [RCV004147595]	uncertain significance	3	122552533	122552533	Human		name
156197456	CV2293571	single nucleotide variant	NM_001146105.2(PARP9):c.458T>A (p.Leu153His)	not specified [RCV004153095]	uncertain significance	3	122555713	122555713	Human		name
156013899	CV2300488	single nucleotide variant	NM_001146105.2(PARP9):c.924T>G (p.Ile308Met)	not specified [RCV004153673]	uncertain significance	3	122552601	122552601	Human		name
156252683	CV2311391	single nucleotide variant	NM_001146105.2(PARP9):c.892G>A (p.Val298Ile)	not specified [RCV004166451]	uncertain significance	3	122552633	122552633	Human		name
155913298	CV2341750	single nucleotide variant	NM_001146105.2(PARP9):c.884C>T (p.Thr295Met)	not specified [RCV004182665]	uncertain significance	3	122555287	122555287	Human		name
156345045	CV2372859	single nucleotide variant	NM_001146105.2(PARP9):c.452G>A (p.Gly151Glu)	not specified [RCV004223909]	uncertain significance	3	122555719	122555719	Human		name
401880376	CV2763019	single nucleotide variant	NM_001146105.2(PARP9):c.980C>T (p.Ser327Leu)	not specified [RCV004342762]	uncertain significance	3	122552545	122552545	Human		name
401879605	CV2764948	single nucleotide variant	NM_001146105.2(PARP9):c.824A>G (p.Asn275Ser)	not specified [RCV004335033]	uncertain significance	3	122555347	122555347	Human		name
401861324	CV2779631	single nucleotide variant	NM_001146105.2(PARP9):c.658A>G (p.Ile220Val)	not specified [RCV004351334]	uncertain significance	3	122555513	122555513	Human		name
405773655	CV3374664	single nucleotide variant	NM_001146105.2(PARP9):c.493C>T (p.Arg165Trp)	not specified [RCV004502723]	uncertain significance	3	122555678	122555678	Human		name
405773674	CV3374667	single nucleotide variant	NM_001146105.2(PARP9):c.734A>G (p.Asn245Ser)	not specified [RCV004502726]	uncertain significance	3	122555437	122555437	Human		name
598244309	CV4002160	single nucleotide variant	NM_001146105.2(PARP9):c.704G>A (p.Ser235Asn)	not specified [RCV005383725]	uncertain significance	3	122555467	122555467	Human		name
156141521	CV2199938	single nucleotide variant	NM_001146105.2(PARP9):c.1694T>C (p.Ile565Thr)	not specified [RCV004074114]	uncertain significance	3	122540543	122540543	Human		name
156099330	CV2250667	single nucleotide variant	NM_001146105.2(PARP9):c.1623T>G (p.Ile541Met)	not specified [RCV004129294]	likely benign	3	122540614	122540614	Human		name
156060023	CV2284394	single nucleotide variant	NM_001146105.2(PARP9):c.2213A>G (p.Gln738Arg)	not specified [RCV004146732]	uncertain significance	3	122528611	122528611	Human		name
156268549	CV2314798	single nucleotide variant	NM_001146105.2(PARP9):c.2252C>T (p.Pro751Leu)	not specified [RCV004170927]	uncertain significance	3	122528572	122528572	Human		name
156187658	CV2318913	single nucleotide variant	NM_001146105.2(PARP9):c.2260A>G (p.Ile754Val)	not specified [RCV004175809]	likely benign	3	122528564	122528564	Human		name
156274741	CV2334137	single nucleotide variant	NM_001146105.2(PARP9):c.1784A>C (p.Gln595Pro)	not specified [RCV004183649]	uncertain significance	3	122537055	122537055	Human		name
155915214	CV2339082	single nucleotide variant	NM_001146105.2(PARP9):c.1817T>A (p.Ile606Asn)	not specified [RCV004187128]	uncertain significance	3	122537022	122537022	Human		name
155938145	CV2364975	single nucleotide variant	NM_001146105.2(PARP9):c.2168T>C (p.Leu723Pro)	not specified [RCV004222268]	uncertain significance	3	122528656	122528656	Human		name
155936142	CV2380296	single nucleotide variant	NM_001146105.2(PARP9):c.1408A>C (p.Lys470Gln)	not specified [RCV004224646]	uncertain significance	3	122540829	122540829	Human		name
329369555	CV2424857	single nucleotide variant	NM_001146105.2(PARP9):c.1756C>T (p.Arg586Cys)	not specified [RCV004248742]	uncertain significance	3	122540481	122540481	Human		name
401732290	CV2708761	single nucleotide variant	NM_001146105.2(PARP9):c.1211A>G (p.Lys404Arg)	not specified [RCV004307727]	uncertain significance	3	122550699	122550699	Human		name
401767477	CV2727176	single nucleotide variant	NM_001146105.2(PARP9):c.1367G>A (p.Ser456Asn)	not specified [RCV004325530]	uncertain significance	3	122545449	122545449	Human		name
405773571	CV3374650	single nucleotide variant	NM_001146105.2(PARP9):c.1024T>A (p.Leu342Met)	not specified [RCV004502709]	uncertain significance	3	122552501	122552501	Human		name
405773577	CV3374651	single nucleotide variant	NM_001146105.2(PARP9):c.1108A>G (p.Ile370Val)	not specified [RCV004502710]	uncertain significance	3	122550802	122550802	Human		name
405773583	CV3374652	single nucleotide variant	NM_001146105.2(PARP9):c.1205T>C (p.Ile402Thr)	not specified [RCV004502711]	uncertain significance	3	122550705	122550705	Human		name
405773595	CV3374654	single nucleotide variant	NM_001146105.2(PARP9):c.1463A>G (p.Asn488Ser)	not specified [RCV004502713]	uncertain significance	3	122540774	122540774	Human		name
405773601	CV3374655	single nucleotide variant	NM_001146105.2(PARP9):c.1474A>G (p.Met492Val)	not specified [RCV004502714]	uncertain significance	3	122540763	122540763	Human		name
405773608	CV3374656	single nucleotide variant	NM_001146105.2(PARP9):c.1679A>T (p.Glu560Val)	not specified [RCV004502715]	uncertain significance	3	122540558	122540558	Human		name
405773613	CV3374657	single nucleotide variant	NM_001146105.2(PARP9):c.1745G>T (p.Arg582Leu)	not specified [RCV004502716]	uncertain significance	3	122540492	122540492	Human		name
405773618	CV3374658	single nucleotide variant	NM_001146105.2(PARP9):c.2222C>T (p.Pro741Leu)	not specified [RCV004502717]	uncertain significance	3	122528602	122528602	Human		name
405773624	CV3374659	single nucleotide variant	NM_001146105.2(PARP9):c.2227A>G (p.Asn743Asp)	not specified [RCV004502718]	uncertain significance	3	122528597	122528597	Human		name
405773632	CV3374660	single nucleotide variant	NM_001146105.2(PARP9):c.2234T>C (p.Val745Ala)	not specified [RCV004502719]	uncertain significance	3	122528590	122528590	Human		name
405773643	CV3374662	single nucleotide variant	NM_001146105.2(PARP9):c.2384A>G (p.Asp795Gly)	not specified [RCV004502721]	uncertain significance	3	122528440	122528440	Human		name
405773649	CV3374663	single nucleotide variant	NM_001146105.2(PARP9):c.2437G>A (p.Ala813Thr)	not specified [RCV004502722]	likely benign	3	122528387	122528387	Human		name
407479755	CV3466641	single nucleotide variant	NM_001146105.2(PARP9):c.1543C>T (p.His515Tyr)	not specified [RCV004664211]	uncertain significance	3	122540694	122540694	Human		name
597675387	CV3568220	single nucleotide variant	NM_001146105.2(PARP9):c.1757G>A (p.Arg586His)	not specified [RCV004830255]	uncertain significance	3	122540480	122540480	Human		name
597670814	CV3568221	single nucleotide variant	NM_001146105.2(PARP9):c.1704G>A (p.Met568Ile)	not specified [RCV004836299]	uncertain significance	3	122540533	122540533	Human		name
597670823	CV3568222	single nucleotide variant	NM_001146105.2(PARP9):c.1696G>C (p.Glu566Gln)	not specified [RCV004836300]	uncertain significance	3	122540541	122540541	Human		name
597670842	CV3568224	single nucleotide variant	NM_001146105.2(PARP9):c.2246T>C (p.Leu749Pro)	not specified [RCV004836302]	uncertain significance	3	122528578	122528578	Human		name
598244318	CV4002162	single nucleotide variant	NM_001146105.2(PARP9):c.1147A>C (p.Ile383Leu)	not specified [RCV005383726]	likely benign	3	122550763	122550763	Human		name
598244325	CV4002163	single nucleotide variant	NM_001146105.2(PARP9):c.2218C>T (p.His740Tyr)	not specified [RCV005383727]	uncertain significance	3	122528606	122528606	Human		name
598244332	CV4002164	single nucleotide variant	NM_001146105.2(PARP9):c.1055T>C (p.Phe352Ser)	not specified [RCV005383728]	likely benign	3	122552470	122552470	Human		name
15177102	CV708504	single nucleotide variant	NM_001146105.2(PARP9):c.1846A>G (p.Thr616Ala)	not provided [RCV000973344]	benign	3	122536993	122536993	Human		name
15121931	CV708505	single nucleotide variant	NM_001146105.2(PARP9):c.1213G>A (p.Glu405Lys)	not provided [RCV000962984]	benign	3	122550697	122550697	Human		name
41405204	CV981415	single nucleotide variant	NM_001146105.2(PARP9):c.2387A>C (p.Tyr796Ser)	not provided [RCV001812460]\|not specified [RCV004035534]	uncertain significance	3	122528437	122528437	Human		name
41405477	CV981416	single nucleotide variant	NM_001146105.2(PARP9):c.2385T>A (p.Asp795Glu)	not provided [RCV001813015]\|not specified [RCV004035538]	uncertain significance	3	122528439	122528439	Human		name
41407414	CV981417	single nucleotide variant	NM_001146105.2(PARP9):c.1652T>C (p.Ile551Thr)	not provided [RCV001810701]	uncertain significance	3	122540585	122540585	Human		name

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