Ddx25 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 Ddx25

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
150499300	CV1235708	single nucleotide variant	NM_013264.5(DDX25):c.*280T>G	not provided [RCV001656391]	benign	11	125923161	125923161	Human		name
15192804	CV730744	single nucleotide variant	NM_013264.5(DDX25):c.508-6C>T	not provided [RCV000888765]	benign	11	125910358	125910358	Human		name
150334187	CV1172207	single nucleotide variant	NM_013264.5(DDX25):c.507+53T>A	not provided [RCV001539855]	benign	11	125908556	125908556	Human		name
150335114	CV1172208	single nucleotide variant	NM_013264.5(DDX25):c.508-65C>T	not provided [RCV001540411]	benign	11	125910299	125910299	Human		name
150494366	CV1238854	single nucleotide variant	NM_013264.5(DDX25):c.404+36T>C	not provided [RCV001655398]	benign	11	125908324	125908324	Human		name
150480022	CV1258353	single nucleotide variant	NM_013264.5(DDX25):c.507+55G>T	not provided [RCV001685772]	benign	11	125908558	125908558	Human		name
150433814	CV1217019	single nucleotide variant	NM_013264.5(DDX25):c.311+155G>C	not provided [RCV001608921]	benign	11	125906364	125906364	Human		name
150494900	CV1224978	single nucleotide variant	NM_013264.5(DDX25):c.1202-69C>T	not provided [RCV001619456]	benign	11	125921122	125921122	Human		name
150497979	CV1236449	single nucleotide variant	NM_013264.5(DDX25):c.508-343G>A	not provided [RCV001656174]	benign	11	125910021	125910021	Human		name
150469283	CV1249069	single nucleotide variant	NM_013264.5(DDX25):c.311+263C>T	not provided [RCV001670831]	benign	11	125906472	125906472	Human		name
150468649	CV1257081	single nucleotide variant	NM_013264.5(DDX25):c.508-154A>C	not provided [RCV001670727]	benign	11	125910210	125910210	Human		name
150455578	CV1268954	single nucleotide variant	NM_013264.5(DDX25):c.312-141G>T	not provided [RCV001692778]	benign	11	125908055	125908055	Human		name
150331829	CV1163555	single nucleotide variant	NM_013264.5(DDX25):c.1038+297C>T	not provided [RCV001527965]	benign	11	125917548	125917548	Human		name
150331164	CV1169438	single nucleotide variant	NM_013264.5(DDX25):c.1039-268C>A	not provided [RCV001536369]	benign	11	125918360	125918360	Human		name
150517497	CV1226947	single nucleotide variant	NM_013264.5(DDX25):c.1391-299T>C	not provided [RCV001640043]	benign	11	125922521	125922521	Human		name
150514104	CV1228056	single nucleotide variant	NM_013264.5(DDX25):c.1038+315G>A	not provided [RCV001638334]	benign	11	125917566	125917566	Human		name
150514138	CV1228072	single nucleotide variant	NM_013264.5(DDX25):c.1201+300G>A	not provided [RCV001638350]	benign	11	125919090	125919090	Human		name
150484939	CV1261991	single nucleotide variant	NM_013264.5(DDX25):c.1390+242C>T	not provided [RCV001686682]	benign	11	125921621	125921621	Human		name
150513414	CV1285158	single nucleotide variant	NM_013264.5(DDX25):c.1038+333A>C	not provided [RCV001722028]	benign	11	125917584	125917584	Human		name
150444040	CV1216575	microsatellite	NM_013264.5(DDX25):c.1202-271AC[15]	not provided [RCV001610874]	benign	11	125920920	125920923	Human		name
150467728	CV1255954	single nucleotide variant	NM_001330438.2(DDX25):c.-280+632G>C	not provided [RCV001670588]	benign	11	125904062	125904062	Human		name
150487178	CV1262696	single nucleotide variant	NM_001330438.2(DDX25):c.-280+761G>T	not provided [RCV001687094]	benign	11	125904191	125904191	Human		name
150444732	CV1266573	microsatellite	NM_013264.5(DDX25):c.1202-271AC[12]	not provided [RCV001691010]	benign	11	125920920	125920929	Human		name
150513445	CV1285168	single nucleotide variant	NM_001330438.2(DDX25):c.-280+726C>T	not provided [RCV001722038]	benign	11	125904156	125904156	Human		name
401747583	CV2688952	single nucleotide variant	NM_013264.5(DDX25):c.27C>G (p.Asp9Glu)	not specified [RCV004303952]	uncertain significance	11	125904544	125904544	Human		name
401724844	CV2693440	single nucleotide variant	NM_013264.5(DDX25):c.11T>C (p.Leu4Ser)	not specified [RCV004295390]	uncertain significance	11	125904528	125904528	Human		name
401722284	CV2706453	single nucleotide variant	NM_013264.5(DDX25):c.18G>C (p.Trp6Cys)	not specified [RCV004317273]	uncertain significance	11	125904535	125904535	Human		name
150476813	CV1239939	single nucleotide variant	NM_013264.5(DDX25):c.804T>G (p.Ala268=)	not provided [RCV001652117]	benign	11	125917017	125917017	Human		name
401883408	CV2785583	single nucleotide variant	NM_013264.5(DDX25):c.49C>T (p.Arg17Trp)	not specified [RCV004363095]	uncertain significance	11	125904566	125904566	Human		name
405704812	CV3243710	single nucleotide variant	NM_013264.5(DDX25):c.801A>G (p.Arg267=)	not specified [RCV004375766]	likely benign	11	125917014	125917014	Human		name
407458631	CV3426581	single nucleotide variant	NM_013264.5(DDX25):c.44G>C (p.Ser15Thr)	not specified [RCV004611627]	uncertain significance	11	125904561	125904561	Human		name
597805681	CV3662068	single nucleotide variant	NM_013264.5(DDX25):c.67T>C (p.Ser23Pro)	not specified [RCV004908733]	uncertain significance	11	125905215	125905215	Human		name
15160035	CV701649	single nucleotide variant	NM_013264.5(DDX25):c.414C>T (p.Asn138=)	not provided [RCV000947399]	benign	11	125908410	125908410	Human		name
150511503	CV1212762	single nucleotide variant	NM_013264.5(DDX25):c.1194T>C (p.Cys398=)	not provided [RCV001597994]	benign	11	125918783	125918783	Human		name
401731028	CV2707661	single nucleotide variant	NM_013264.5(DDX25):c.272C>G (p.Ser91Cys)	not specified [RCV004306923]	uncertain significance	11	125906170	125906170	Human		name
405704764	CV3243704	single nucleotide variant	NM_013264.5(DDX25):c.111T>A (p.Ser37Arg)	not specified [RCV004375760]	uncertain significance	11	125905259	125905259	Human		name
405704771	CV3243705	single nucleotide variant	NM_013264.5(DDX25):c.137C>T (p.Ser46Phe)	not specified [RCV004375761]	uncertain significance	11	125905559	125905559	Human		name
598263304	CV3960065	single nucleotide variant	NM_013264.5(DDX25):c.178G>C (p.Asp60His)	not specified [RCV005325662]	uncertain significance	11	125906076	125906076	Human		name
156342761	CV2222462	single nucleotide variant	NM_013264.5(DDX25):c.852C>G (p.Asp284Glu)	not specified [RCV004099314]	uncertain significance	11	125917065	125917065	Human		name
155917333	CV2236526	single nucleotide variant	NM_013264.5(DDX25):c.502C>T (p.Pro168Ser)	not specified [RCV004110523]	uncertain significance	11	125908498	125908498	Human		name
155963690	CV2254601	single nucleotide variant	NM_013264.5(DDX25):c.563A>G (p.Glu188Gly)	not specified [RCV004123945]	uncertain significance	11	125910419	125910419	Human		name
156144294	CV2268858	single nucleotide variant	NM_013264.5(DDX25):c.937C>T (p.Arg313Trp)	not specified [RCV004126144]	uncertain significance	11	125917150	125917150	Human		name
156053112	CV2269473	single nucleotide variant	NM_013264.5(DDX25):c.782A>C (p.His261Pro)	not specified [RCV004124586]	uncertain significance	11	125911470	125911470	Human		name
156160717	CV2272534	single nucleotide variant	NM_013264.5(DDX25):c.626C>T (p.Pro209Leu)	not specified [RCV004133433]	uncertain significance	11	125911314	125911314	Human		name
156135965	CV2357075	single nucleotide variant	NM_013264.5(DDX25):c.907C>T (p.Arg303Cys)	not specified [RCV004206875]	uncertain significance	11	125917120	125917120	Human		name
329388938	CV2448514	single nucleotide variant	NM_013264.5(DDX25):c.465G>C (p.Leu155Phe)	not specified [RCV004259200]	uncertain significance	11	125908461	125908461	Human		name
329395753	CV2454525	single nucleotide variant	NM_013264.5(DDX25):c.769G>A (p.Gly257Arg)	not specified [RCV004268014]	uncertain significance	11	125911457	125911457	Human		name
401729591	CV2690360	single nucleotide variant	NM_013264.5(DDX25):c.475A>G (p.Ser159Gly)	not specified [RCV004302354]	uncertain significance	11	125908471	125908471	Human		name
401886075	CV2771060	single nucleotide variant	NM_013264.5(DDX25):c.674C>T (p.Thr225Ile)	not specified [RCV004346069]	uncertain significance	11	125911362	125911362	Human		name
405704779	CV3243706	single nucleotide variant	NM_013264.5(DDX25):c.377T>C (p.Met126Thr)	not specified [RCV004375762]	uncertain significance	11	125908261	125908261	Human		name
405704786	CV3243707	single nucleotide variant	NM_013264.5(DDX25):c.490T>G (p.Leu164Val)	not specified [RCV004375763]	uncertain significance	11	125908486	125908486	Human		name
405704798	CV3243708	single nucleotide variant	NM_013264.5(DDX25):c.635C>A (p.Thr212Asn)	not specified [RCV004375764]	uncertain significance	11	125911323	125911323	Human		name
405704806	CV3243709	single nucleotide variant	NM_013264.5(DDX25):c.797A>G (p.Gln266Arg)	not specified [RCV004375765]	uncertain significance	11	125911485	125911485	Human		name
407458638	CV3426583	single nucleotide variant	NM_013264.5(DDX25):c.557T>G (p.Val186Gly)	not specified [RCV004611629]	uncertain significance	11	125910413	125910413	Human		name
597805677	CV3662064	single nucleotide variant	NM_013264.5(DDX25):c.474A>C (p.Leu158Phe)	not specified [RCV004908729]	uncertain significance	11	125908470	125908470	Human		name
597805680	CV3662067	single nucleotide variant	NM_013264.5(DDX25):c.959A>G (p.Glu320Gly)	not specified [RCV004908732]	uncertain significance	11	125917172	125917172	Human		name
597805682	CV3662069	single nucleotide variant	NM_013264.5(DDX25):c.665C>G (p.Thr222Ser)	not specified [RCV004908734]	uncertain significance	11	125911353	125911353	Human		name
598160590	CV3960066	single nucleotide variant	NM_013264.5(DDX25):c.960G>T (p.Glu320Asp)	not specified [RCV005328805]	uncertain significance	11	125917173	125917173	Human		name
598263306	CV3960067	single nucleotide variant	NM_013264.5(DDX25):c.481G>C (p.Val161Leu)	not specified [RCV005325663]	uncertain significance	11	125908477	125908477	Human		name
151236188	CV1319633	single nucleotide variant	NM_013264.5(DDX25):c.1129C>T (p.Arg377Ter)	Azoospermia [RCV001797569]	pathogenic	11	125918718	125918718	Human	2	name
156103858	CV2310830	single nucleotide variant	NM_013264.5(DDX25):c.1130G>C (p.Arg377Pro)	not specified [RCV004163878]	uncertain significance	11	125918719	125918719	Human		name
156287776	CV2327350	single nucleotide variant	NM_013264.5(DDX25):c.1324G>A (p.Gly442Ser)	not specified [RCV004174784]	uncertain significance	11	125921313	125921313	Human		name
156226386	CV2352736	single nucleotide variant	NM_013264.5(DDX25):c.1300C>T (p.Arg434Trp)	not specified [RCV004198758]	uncertain significance	11	125921289	125921289	Human		name
156402183	CV2368120	single nucleotide variant	NM_013264.5(DDX25):c.1062G>T (p.Leu354Phe)	not specified [RCV004216469]	uncertain significance	11	125918651	125918651	Human		name
329361375	CV2459405	single nucleotide variant	NM_013264.5(DDX25):c.1319A>T (p.Lys440Ile)	not specified [RCV004275099]	uncertain significance	11	125921308	125921308	Human		name
401719385	CV2679517	single nucleotide variant	NM_013264.5(DDX25):c.1043G>A (p.Arg348His)	not specified [RCV004287820]	uncertain significance	11	125918632	125918632	Human		name
401726962	CV2684409	single nucleotide variant	NM_013264.5(DDX25):c.1414G>A (p.Ala472Thr)	not specified [RCV004291487]	uncertain significance	11	125922843	125922843	Human		name
401893226	CV2766250	single nucleotide variant	NM_013264.5(DDX25):c.1120G>A (p.Val374Met)	not specified [RCV004340685]	uncertain significance	11	125918709	125918709	Human		name
407458635	CV3426582	single nucleotide variant	NM_013264.5(DDX25):c.1081G>T (p.Asp361Tyr)	not specified [RCV004611628]	uncertain significance	11	125918670	125918670	Human		name
597805678	CV3662065	single nucleotide variant	NM_013264.5(DDX25):c.1066G>A (p.Val356Met)	not specified [RCV004908730]	uncertain significance	11	125918655	125918655	Human		name
597805679	CV3662066	single nucleotide variant	NM_013264.5(DDX25):c.1204A>T (p.Ile402Phe)	not specified [RCV004908731]	uncertain significance	11	125921193	125921193	Human		name
598263302	CV3960064	single nucleotide variant	NM_013264.5(DDX25):c.1046G>A (p.Arg349Gln)	not specified [RCV005325661]	likely benign	11	125918635	125918635	Human		name
617150003	CV4021598	single nucleotide variant	NM_013264.5(DDX25):c.1216C>T (p.Gln406Ter)	not provided [RCV005425567]	uncertain significance	11	125921205	125921205	Human		name
150493568	CV1238695	microsatellite	NM_001330438.2(DDX25):c.-280+872_-280+890del	not provided [RCV001655239]	benign	11	125904266	125904284	Human		name

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