Rad9 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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74 records found for search term Rad9

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15199723	CV702110	deletion	NM_001286535.2(RAD9B):c.934_937del	not provided [RCV000957120]	benign	12	110531584	110531587	Human		name
405266096	CV3201885	single nucleotide variant	NM_001286535.2(RAD9B):c.331A>C (p.Arg111=)	RAD9B-related disorder [RCV003911375]	likely benign	12	110506636	110506636	Human		name , trait , alternate_id
405271983	CV3206369	single nucleotide variant	NM_001286535.2(RAD9B):c.176C>T (p.Pro59Leu)	RAD9B-related disorder [RCV003971985]	likely benign	12	110505675	110505675	Human		name , trait , alternate_id
405276474	CV3206710	single nucleotide variant	NM_001286535.2(RAD9B):c.526C>G (p.Gln176Glu)	RAD9B-related disorder [RCV003917147]	likely benign	12	110515087	110515087	Human		name , trait , alternate_id
407485434	CV3472110	single nucleotide variant	NM_004584.3(RAD9A):c.13G>C (p.Val5Leu)	not specified [RCV004665296]	uncertain significance	11	67392057	67392057	Human		name
597753339	CV3582419	single nucleotide variant	NM_004584.3(RAD9A):c.49G>A (p.Val17Ile)	not specified [RCV004847057]	uncertain significance	11	67392175	67392175	Human		name
598173991	CV3905098	single nucleotide variant	NM_004584.3(RAD9A):c.53A>G (p.His18Arg)	not specified [RCV005263784]	uncertain significance	11	67392179	67392179	Human		name
156082397	CV2292916	single nucleotide variant	NM_004584.3(RAD9A):c.262G>A (p.Ala88Thr)	not specified [RCV004148412]	uncertain significance	11	67393523	67393523	Human		name
405691921	CV3319066	single nucleotide variant	NM_004584.3(RAD9A):c.221A>G (p.Lys74Arg)	not specified [RCV004445507]	uncertain significance	11	67392769	67392769	Human		name
597684477	CV3582420	single nucleotide variant	NM_004584.3(RAD9A):c.209T>A (p.Leu70Gln)	not specified [RCV004858178]	uncertain significance	11	67392757	67392757	Human		name
156165070	CV2243437	single nucleotide variant	NM_004584.3(RAD9A):c.818A>G (p.Gln273Arg)	not specified [RCV004112408]	uncertain significance	11	67396346	67396346	Human		name
156060643	CV2263066	single nucleotide variant	NM_004584.3(RAD9A):c.311G>A (p.Arg104Gln)	not specified [RCV004131321]	uncertain significance	11	67393572	67393572	Human		name
156175113	CV2299520	single nucleotide variant	NM_004584.3(RAD9A):c.409G>A (p.Asp137Asn)	not specified [RCV004154864]	uncertain significance	11	67393750	67393750	Human		name
156255258	CV2325730	single nucleotide variant	NM_001286535.2(RAD9B):c.10A>G (p.Met4Val)	not specified [RCV004173626]	uncertain significance	12	110502347	110502347	Human		name
156079246	CV2337257	single nucleotide variant	NM_004584.3(RAD9A):c.695C>T (p.Ala232Val)	not specified [RCV004185711]	uncertain significance	11	67396136	67396136	Human		name
156145871	CV2357894	single nucleotide variant	NM_004584.3(RAD9A):c.536G>A (p.Arg179His)	not specified [RCV004209684]	uncertain significance	11	67395802	67395802	Human		name
329384637	CV2435158	single nucleotide variant	NM_004584.3(RAD9A):c.941T>C (p.Ile314Thr)	not specified [RCV004252797]	uncertain significance	11	67397247	67397247	Human		name
329398797	CV2442835	single nucleotide variant	NM_004584.3(RAD9A):c.772G>A (p.Gly258Ser)	not specified [RCV004253449]	uncertain significance	11	67396300	67396300	Human		name
329396665	CV2462860	single nucleotide variant	NM_004584.3(RAD9A):c.412C>T (p.Pro138Ser)	not specified [RCV004272415]	uncertain significance	11	67393753	67393753	Human		name
401738418	CV2676277	single nucleotide variant	NM_004584.3(RAD9A):c.341G>C (p.Cys114Ser)	not specified [RCV004286315]	uncertain significance	11	67393602	67393602	Human		name
401742235	CV2676924	single nucleotide variant	NM_004584.3(RAD9A):c.310C>T (p.Arg104Trp)	not specified [RCV004291082]	uncertain significance	11	67393571	67393571	Human		name
401724899	CV2715018	single nucleotide variant	NM_004584.3(RAD9A):c.427C>T (p.His143Tyr)	not specified [RCV004322332]	uncertain significance	11	67393768	67393768	Human		name
401898534	CV2788034	single nucleotide variant	NM_004584.3(RAD9A):c.355C>T (p.Arg119Trp)	not specified [RCV004358685]	uncertain significance	11	67393696	67393696	Human		name
401896862	CV2788883	single nucleotide variant	NM_004584.3(RAD9A):c.521G>A (p.Arg174His)	not specified [RCV004362923]	uncertain significance	11	67395787	67395787	Human		name
405691926	CV3319067	single nucleotide variant	NM_004584.3(RAD9A):c.419C>T (p.Ser140Leu)	not specified [RCV004445508]	likely benign	11	67393760	67393760	Human		name
405691933	CV3319068	single nucleotide variant	NM_004584.3(RAD9A):c.437G>A (p.Arg146His)	not specified [RCV004445509]	uncertain significance	11	67393778	67393778	Human		name
405691938	CV3319069	single nucleotide variant	NM_004584.3(RAD9A):c.884C>T (p.Pro295Leu)	not specified [RCV004445510]	likely benign	11	67397190	67397190	Human		name
405691943	CV3319070	single nucleotide variant	NM_004584.3(RAD9A):c.985C>T (p.Pro329Ser)	not specified [RCV004445511]	uncertain significance	11	67397291	67397291	Human		name
405691950	CV3319071	single nucleotide variant	NM_001286535.2(RAD9B):c.26T>C (p.Met9Thr)	not specified [RCV004445512]	uncertain significance	12	110502363	110502363	Human		name
407485429	CV3472109	single nucleotide variant	NM_004584.3(RAD9A):c.542A>G (p.Tyr181Cys)	not specified [RCV004665295]	uncertain significance	11	67395808	67395808	Human		name
597684452	CV3582414	single nucleotide variant	NM_004584.3(RAD9A):c.991C>T (p.Pro331Ser)	not specified [RCV004858175]	uncertain significance	11	67397297	67397297	Human		name
597684459	CV3582415	single nucleotide variant	NM_004584.3(RAD9A):c.914C>T (p.Ser305Phe)	not specified [RCV004858176]	uncertain significance	11	67397220	67397220	Human		name
597753332	CV3582416	single nucleotide variant	NM_004584.3(RAD9A):c.554A>C (p.Glu185Ala)	not specified [RCV004847055]	uncertain significance	11	67395820	67395820	Human		name
598173983	CV3905097	single nucleotide variant	NM_004584.3(RAD9A):c.403G>A (p.Val135Ile)	not specified [RCV005263783]	uncertain significance	11	67393744	67393744	Human		name
598173999	CV3905099	single nucleotide variant	NM_004584.3(RAD9A):c.446C>T (p.Ala149Val)	not specified [RCV005263785]	uncertain significance	11	67393787	67393787	Human		name
155976506	CV2211399	single nucleotide variant	NM_001286535.2(RAD9B):c.77G>A (p.Arg26Gln)	not specified [RCV004090314]	uncertain significance	12	110503836	110503836	Human		name
156379993	CV2218018	single nucleotide variant	NM_004584.3(RAD9A):c.1120C>T (p.Arg374Cys)	not specified [RCV004086463]	uncertain significance	11	67397503	67397503	Human		name
156075509	CV2248252	single nucleotide variant	NM_004584.3(RAD9A):c.1127C>T (p.Pro376Leu)	not specified [RCV004119423]	uncertain significance	11	67397510	67397510	Human		name
156253246	CV2390139	single nucleotide variant	NM_001286535.2(RAD9B):c.91T>C (p.Phe31Leu)	not specified [RCV004240527]	likely benign	12	110503850	110503850	Human		name
401899809	CV2758836	single nucleotide variant	NM_004584.3(RAD9A):c.1084C>T (p.Arg362Cys)	not specified [RCV004339929]	uncertain significance	11	67397467	67397467	Human		name
401884240	CV2761607	single nucleotide variant	NM_004584.3(RAD9A):c.1039G>A (p.Ala347Thr)	not specified [RCV004337233]	uncertain significance	11	67397345	67397345	Human		name
597753335	CV3582417	single nucleotide variant	NM_004584.3(RAD9A):c.1136C>A (p.Pro379His)	not specified [RCV004847056]	uncertain significance	11	67397519	67397519	Human		name
597684469	CV3582418	single nucleotide variant	NM_004584.3(RAD9A):c.1151C>T (p.Ala384Val)	not specified [RCV004858177]	uncertain significance	11	67397534	67397534	Human		name
597684485	CV3582421	single nucleotide variant	NM_004584.3(RAD9A):c.1097T>C (p.Phe366Ser)	not specified [RCV004858179]	uncertain significance	11	67397480	67397480	Human		name
15040571	CV682324	single nucleotide variant	NM_001286535.2(RAD9B):c.28A>G (p.Ser10Gly)	Neural tube defect [RCV000855731]	likely pathogenic	12	110502365	110502365	Human	2	name
329361003	CV2439931	single nucleotide variant	NM_001286535.2(RAD9B):c.124C>G (p.Leu42Val)	not specified [RCV004257964]	uncertain significance	12	110505623	110505623	Human		name
329366494	CV2445779	single nucleotide variant	NM_001286535.2(RAD9B):c.220A>C (p.Ser74Arg)	not specified [RCV004259837]	uncertain significance	12	110505719	110505719	Human		name
401781722	CV2722241	single nucleotide variant	NM_001286535.2(RAD9B):c.173C>G (p.Ser58Cys)	not specified [RCV004328799]	uncertain significance	12	110505672	110505672	Human		name
401894397	CV2777130	single nucleotide variant	NM_001286535.2(RAD9B):c.224A>C (p.Glu75Ala)	not specified [RCV004354180]	uncertain significance	12	110505723	110505723	Human		name
597753348	CV3582424	single nucleotide variant	NM_001286535.2(RAD9B):c.137A>C (p.Asn46Thr)	not specified [RCV004847059]	uncertain significance	12	110505636	110505636	Human		name
598174011	CV3905101	single nucleotide variant	NM_001286535.2(RAD9B):c.169T>C (p.Phe57Leu)	not specified [RCV005263787]	uncertain significance	12	110505668	110505668	Human		name
26902523	CV682326	deletion	NM_001286535.2(RAD9B):c.960del (p.Ala321fs)	Neural tube defect [RCV001089480]	pathogenic	12	110522240	110522240	Human	2	name
155936846	CV2379916	single nucleotide variant	NM_001286535.2(RAD9B):c.665T>G (p.Met222Arg)	not specified [RCV004222064]	uncertain significance	12	110518745	110518745	Human		name
329380115	CV2466430	single nucleotide variant	NM_001286535.2(RAD9B):c.596A>C (p.Asp199Ala)	not specified [RCV004273987]	uncertain significance	12	110518676	110518676	Human		name
401731855	CV2674500	single nucleotide variant	NM_001286535.2(RAD9B):c.389G>T (p.Gly130Val)	not specified [RCV004291383]	uncertain significance	12	110512779	110512779	Human		name
401726946	CV2674612	single nucleotide variant	NM_001286535.2(RAD9B):c.335T>C (p.Ile112Thr)	not specified [RCV004291482]	uncertain significance	12	110506640	110506640	Human		name
401731592	CV2712058	single nucleotide variant	NM_001286535.2(RAD9B):c.623T>C (p.Met208Thr)	not specified [RCV004311798]	uncertain significance	12	110518703	110518703	Human		name
401865693	CV2778892	single nucleotide variant	NM_001286535.2(RAD9B):c.574A>G (p.Ser192Gly)	not specified [RCV004346775]	uncertain significance	12	110515135	110515135	Human		name
405691955	CV3319072	single nucleotide variant	NM_001286535.2(RAD9B):c.605A>G (p.Asn202Ser)	not specified [RCV004445513]	likely benign	12	110518685	110518685	Human		name
405691961	CV3319073	single nucleotide variant	NM_001286535.2(RAD9B):c.977T>C (p.Leu326Pro)	not specified [RCV004445514]	uncertain significance	12	110522263	110522263	Human		name
407485443	CV3472116	single nucleotide variant	NM_001286535.2(RAD9B):c.847G>A (p.Ala283Thr)	not specified [RCV004665298]	uncertain significance	12	110519873	110519873	Human		name
597684508	CV3582425	single nucleotide variant	NM_001286535.2(RAD9B):c.860A>G (p.Gln287Arg)	not specified [RCV004858181]	uncertain significance	12	110519886	110519886	Human		name
598174005	CV3905100	single nucleotide variant	NM_001286535.2(RAD9B):c.646G>A (p.Asp216Asn)	not specified [RCV005263786]	uncertain significance	12	110518726	110518726	Human		name
15040568	CV682205	single nucleotide variant	NM_001286535.2(RAD9B):c.661G>A (p.Gly221Arg)	Neural tube defect [RCV000855674]	likely pathogenic	12	110518741	110518741	Human	2	name
15040569	CV682207	single nucleotide variant	NM_001286535.2(RAD9B):c.336A>G (p.Ile112Met)	Neural tube defect [RCV000855676]	likely pathogenic	12	110506641	110506641	Human	2	name
15040572	CV682325	single nucleotide variant	NM_001286535.2(RAD9B):c.645T>A (p.Phe215Leu)	Neural tube defect [RCV000855732]	likely pathogenic	12	110518725	110518725	Human	2	name
15040565	CV682345	duplication	NM_001286535.2(RAD9B):c.1199dup (p.Arg401fs)	Neural tube defect [RCV000855752]	pathogenic	12	110530597	110530598	Human	2	name
156116627	CV2282959	single nucleotide variant	NM_001286535.2(RAD9B):c.1178A>C (p.Asn393Thr)	not specified [RCV004143595]	uncertain significance	12	110530577	110530577	Human		name
407500232	CV3472113	single nucleotide variant	NM_001286535.2(RAD9B):c.1140C>A (p.Phe380Leu)	not specified [RCV004669508]	uncertain significance	12	110530539	110530539	Human		name
407500236	CV3472114	single nucleotide variant	NM_001286535.2(RAD9B):c.1090A>T (p.Thr364Ser)	not specified [RCV004669509]	uncertain significance	12	110522376	110522376	Human		name
407500241	CV3472115	single nucleotide variant	NM_001286535.2(RAD9B):c.1030C>T (p.Pro344Ser)	not specified [RCV004669510]	uncertain significance	12	110522316	110522316	Human		name
597684496	CV3582423	single nucleotide variant	NM_001286535.2(RAD9B):c.1124A>T (p.Lys375Met)	not specified [RCV004858180]	uncertain significance	12	110522410	110522410	Human		name
597684518	CV3582426	single nucleotide variant	NM_001286535.2(RAD9B):c.1145G>A (p.Gly382Glu)	not specified [RCV004858182]	uncertain significance	12	110530544	110530544	Human		name
15040570	CV682208	single nucleotide variant	NM_001286535.2(RAD9B):c.1060A>G (p.Ser354Gly)	Neural tube defect [RCV000855677]	likely pathogenic	12	110522346	110522346	Human	2	name

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