Ddx10 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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104 records found for search term Ddx10

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405292046	CV3207860	single nucleotide variant	NM_004398.4(DDX10):c.378+7A>G	DDX10-related disorder [RCV003929536]	benign	11	108675733	108675733	Human		name , trait , alternate_id
405271968	CV3203019	single nucleotide variant	NM_004398.4(DDX10):c.1139-4G>A	DDX10-related disorder [RCV003914071]	likely benign	11	108693512	108693512	Human		name , trait , alternate_id
8652523	CV129098	single nucleotide variant	NM_004398.3(DDX10):c.1965+34057G>A	Lung cancer [RCV000109585]	uncertain significance	11	108757519	108757519	Human		name
405285374	CV3212423	single nucleotide variant	NM_004398.4(DDX10):c.240A>G (p.Thr80=)	DDX10-related disorder [RCV003959028]	likely benign	11	108673520	108673520	Human		name , trait , alternate_id
407458425	CV3430479	single nucleotide variant	NM_004398.4(DDX10):c.95A>T (p.Asn32Ile)	not specified [RCV004611580]	uncertain significance	11	108665248	108665248	Human		name
597805616	CV3661980	single nucleotide variant	NM_004398.4(DDX10):c.62A>G (p.Asn21Ser)	not specified [RCV004908668]	uncertain significance	11	108665215	108665215	Human		name
597805620	CV3661985	single nucleotide variant	NM_004398.4(DDX10):c.61A>C (p.Asn21His)	not specified [RCV004908672]	uncertain significance	11	108665214	108665214	Human		name
597805623	CV3661988	single nucleotide variant	NM_004398.4(DDX10):c.40C>T (p.Pro14Ser)	not specified [RCV004908675]	uncertain significance	11	108665193	108665193	Human		name
598160576	CV3959997	single nucleotide variant	NM_004398.4(DDX10):c.40C>G (p.Pro14Ala)	not specified [RCV005328802]	uncertain significance	11	108665193	108665193	Human		name
598263168	CV3960005	single nucleotide variant	NM_004398.4(DDX10):c.38G>C (p.Arg13Pro)	not specified [RCV005325603]	uncertain significance	11	108665191	108665191	Human		name
15176257	CV712593	single nucleotide variant	NM_004398.4(DDX10):c.846T>C (p.Tyr282=)	not provided [RCV000973145]	benign\|likely benign	11	108679558	108679558	Human		name
401741774	CV2697625	single nucleotide variant	NM_004398.4(DDX10):c.296C>T (p.Thr99Ile)	not specified [RCV004298371]	uncertain significance	11	108675644	108675644	Human		name
405286263	CV3192750	single nucleotide variant	NM_004398.4(DDX10):c.1761C>T (p.Asp587=)	DDX10-related disorder [RCV003981498]	likely benign	11	108723258	108723258	Human		name , trait , alternate_id
405272033	CV3203054	single nucleotide variant	NM_004398.4(DDX10):c.1698C>T (p.Leu566=)	DDX10-related disorder [RCV003914106]	benign	11	108723195	108723195	Human		name , trait , alternate_id
405289147	CV3204939	single nucleotide variant	NM_004398.4(DDX10):c.2505C>T (p.Asp835=)	DDX10-related disorder [RCV003961579]	likely benign	11	108940300	108940300	Human		name , trait , alternate_id
405291111	CV3215079	single nucleotide variant	NM_004398.4(DDX10):c.2514A>G (p.Pro838=)	DDX10-related disorder [RCV003927372]	benign	11	108940309	108940309	Human		name , trait , alternate_id
15097779	CV701552	single nucleotide variant	NM_004398.4(DDX10):c.131C>G (p.Pro44Arg)	DDX10-related disorder [RCV003960690]\|not provided [RCV000958392]	benign\|likely benign	11	108665284	108665284	Human		name , trait , alternate_id
15176261	CV712594	single nucleotide variant	NM_004398.4(DDX10):c.1563C>T (p.Thr521=)	DDX10-related disorder [RCV003936160]\|not provided [RCV000973146]	benign\|likely benign	11	108723060	108723060	Human		name , trait , alternate_id
156338513	CV2271284	single nucleotide variant	NM_004398.4(DDX10):c.446C>G (p.Pro149Arg)	not specified [RCV004136410]	uncertain significance	11	108677152	108677152	Human		name
156048390	CV2271720	single nucleotide variant	NM_004398.4(DDX10):c.691G>C (p.Gly231Arg)	not specified [RCV004130567]	uncertain significance	11	108679403	108679403	Human		name
155982301	CV2337144	single nucleotide variant	NM_004398.4(DDX10):c.602T>G (p.Leu201Arg)	not specified [RCV004192903]	uncertain significance	11	108678379	108678379	Human		name
156212826	CV2366993	single nucleotide variant	NM_004398.4(DDX10):c.478G>T (p.Val160Phe)	not specified [RCV004213397]	uncertain significance	11	108677184	108677184	Human		name
156034024	CV2376640	single nucleotide variant	NM_004398.4(DDX10):c.947G>A (p.Ser316Asn)	not specified [RCV004222841]	uncertain significance	11	108689034	108689034	Human		name
329362541	CV2463986	single nucleotide variant	NM_004398.4(DDX10):c.736A>G (p.Lys246Glu)	not specified [RCV004273702]	uncertain significance	11	108679448	108679448	Human		name
401773072	CV2698083	single nucleotide variant	NM_004398.4(DDX10):c.986T>G (p.Leu329Arg)	not specified [RCV004302880]	uncertain significance	11	108691886	108691886	Human		name
405704006	CV3243609	single nucleotide variant	NM_004398.4(DDX10):c.387A>C (p.Glu129Asp)	not specified [RCV004375665]	uncertain significance	11	108677093	108677093	Human		name
405704014	CV3243610	single nucleotide variant	NM_004398.4(DDX10):c.398G>A (p.Arg133His)	not specified [RCV004375666]	uncertain significance	11	108677104	108677104	Human		name
405704022	CV3243611	single nucleotide variant	NM_004398.4(DDX10):c.739C>T (p.Arg247Cys)	not specified [RCV004375667]	uncertain significance	11	108679451	108679451	Human		name
407458430	CV3430481	single nucleotide variant	NM_004398.4(DDX10):c.379G>A (p.Val127Met)	not specified [RCV004611582]	uncertain significance	11	108677085	108677085	Human		name
407458443	CV3430485	single nucleotide variant	NM_004398.4(DDX10):c.397C>T (p.Arg133Cys)	not specified [RCV004611586]	uncertain significance	11	108677103	108677103	Human		name
597805615	CV3661979	single nucleotide variant	NM_004398.4(DDX10):c.640A>G (p.Thr214Ala)	not specified [RCV004908667]	uncertain significance	11	108678417	108678417	Human		name
597805617	CV3661981	single nucleotide variant	NM_004398.4(DDX10):c.401T>G (p.Leu134Arg)	not specified [RCV004908669]	uncertain significance	11	108677107	108677107	Human		name
598263139	CV3959996	single nucleotide variant	NM_004398.4(DDX10):c.991C>G (p.Arg331Gly)	not specified [RCV005325596]	uncertain significance	11	108691891	108691891	Human		name
598263175	CV3960007	single nucleotide variant	NM_004398.4(DDX10):c.994G>C (p.Val332Leu)	not specified [RCV005325605]	uncertain significance	11	108691894	108691894	Human		name
152978485	CV1671659	single nucleotide variant	NM_004398.4(DDX10):c.1609G>A (p.Ala537Thr)	Neurodevelopmental disorder [RCV002227764]	uncertain significance	11	108723106	108723106	Human	1	name
10449788	CV215421	single nucleotide variant	NM_004398.4(DDX10):c.1334A>G (p.Glu445Gly)	DDX10-related disorder [RCV003917827]\|not provided [RCV004706659]\|not specified [RCV000202907]	benign\|likely benign	11	108715890	108715890	Human		name , trait , alternate_id
156397750	CV2197511	single nucleotide variant	NM_004398.4(DDX10):c.1100C>T (p.Ala367Val)	not specified [RCV004081237]	uncertain significance	11	108692000	108692000	Human		name
156143178	CV2208615	single nucleotide variant	NM_004398.4(DDX10):c.1613C>T (p.Pro538Leu)	not specified [RCV004091134]	uncertain significance	11	108723110	108723110	Human		name
156050880	CV2237865	single nucleotide variant	NM_004398.4(DDX10):c.1817C>A (p.Ser606Tyr)	not specified [RCV004109097]	uncertain significance	11	108723314	108723314	Human		name
156195075	CV2251806	single nucleotide variant	NM_004398.4(DDX10):c.1566A>T (p.Lys522Asn)	not specified [RCV004119796]	uncertain significance	11	108723063	108723063	Human		name
156237245	CV2265109	single nucleotide variant	NM_004398.4(DDX10):c.1784A>G (p.Lys595Arg)	not specified [RCV004126246]	uncertain significance	11	108723281	108723281	Human		name
155992796	CV2286232	single nucleotide variant	NM_004398.4(DDX10):c.2533A>G (p.Lys845Glu)	not specified [RCV004146195]	uncertain significance	11	108940328	108940328	Human		name
155992807	CV2286233	single nucleotide variant	NM_004398.4(DDX10):c.2534A>C (p.Lys845Thr)	not specified [RCV004146196]	uncertain significance	11	108940329	108940329	Human		name
156047586	CV2304350	single nucleotide variant	NM_004398.4(DDX10):c.2552T>C (p.Leu851Ser)	not specified [RCV004164464]	uncertain significance	11	108940347	108940347	Human		name
156040103	CV2310767	single nucleotide variant	NM_004398.4(DDX10):c.1796C>G (p.Ala599Gly)	not specified [RCV004157695]	uncertain significance	11	108723293	108723293	Human		name
156147978	CV2321632	single nucleotide variant	NM_004398.4(DDX10):c.2303A>G (p.Lys768Arg)	not specified [RCV004179647]	uncertain significance	11	108852208	108852208	Human		name
156182844	CV2327929	single nucleotide variant	NM_004398.4(DDX10):c.1645A>G (p.Arg549Gly)	not specified [RCV004179249]	uncertain significance	11	108723142	108723142	Human		name
155985205	CV2345038	single nucleotide variant	NM_004398.4(DDX10):c.1924A>G (p.Asn642Asp)	not specified [RCV004193321]	uncertain significance	11	108723421	108723421	Human		name
155924555	CV2352100	single nucleotide variant	NM_004398.4(DDX10):c.2122A>G (p.Ile708Val)	not specified [RCV004191192]	uncertain significance	11	108841351	108841351	Human		name
155928853	CV2363380	single nucleotide variant	NM_004398.4(DDX10):c.1978T>C (p.Ser660Pro)	not specified [RCV004213918]	uncertain significance	11	108838458	108838458	Human		name
155928947	CV2363397	single nucleotide variant	NM_004398.4(DDX10):c.1919G>A (p.Arg640Gln)	not specified [RCV004215982]	uncertain significance	11	108723416	108723416	Human		name
156179700	CV2374698	single nucleotide variant	NM_004398.4(DDX10):c.2147A>G (p.Asp716Gly)	not specified [RCV004225311]	uncertain significance	11	108841376	108841376	Human		name
155937661	CV2380060	single nucleotide variant	NM_004398.4(DDX10):c.2345A>T (p.Asp782Val)	not specified [RCV004222190]	uncertain significance	11	108917913	108917913	Human		name
156257759	CV2383609	single nucleotide variant	NM_004398.4(DDX10):c.1918C>T (p.Arg640Trp)	not specified [RCV004229500]	uncertain significance	11	108723415	108723415	Human		name
155907312	CV2389840	single nucleotide variant	NM_004398.4(DDX10):c.1010G>A (p.Arg337His)	not specified [RCV004236060]	uncertain significance	11	108691910	108691910	Human		name
156007776	CV2390017	single nucleotide variant	NM_004398.4(DDX10):c.1616C>G (p.Ser539Cys)	not specified [RCV004238631]	uncertain significance	11	108723113	108723113	Human		name
329359007	CV2425317	single nucleotide variant	NM_004398.4(DDX10):c.1343T>C (p.Ile448Thr)	not specified [RCV004250983]	uncertain significance	11	108715899	108715899	Human		name
401743373	CV2687935	single nucleotide variant	NM_004398.4(DDX10):c.1687G>A (p.Gly563Arg)	not specified [RCV004305023]	uncertain significance	11	108723184	108723184	Human		name
401742607	CV2697818	single nucleotide variant	NM_004398.4(DDX10):c.1170T>G (p.Phe390Leu)	not specified [RCV004300537]	uncertain significance	11	108693547	108693547	Human		name
401899845	CV2755460	single nucleotide variant	NM_004398.4(DDX10):c.2271A>C (p.Glu757Asp)	not specified [RCV004340049]	uncertain significance	11	108852176	108852176	Human		name
405273642	CV3192207	single nucleotide variant	NM_004398.4(DDX10):c.1723A>G (p.Asn575Asp)	DDX10-related disorder [RCV003914721]	benign	11	108723220	108723220	Human		name , trait , alternate_id
405294916	CV3214945	single nucleotide variant	NM_004398.4(DDX10):c.1964A>G (p.Gln655Arg)	DDX10-related disorder [RCV003936804]	likely benign	11	108723461	108723461	Human		name , trait , alternate_id
405703922	CV3243598	single nucleotide variant	NM_004398.4(DDX10):c.1121T>C (p.Ile374Thr)	not specified [RCV004375654]	uncertain significance	11	108692021	108692021	Human		name
405703929	CV3243599	single nucleotide variant	NM_004398.4(DDX10):c.1424A>G (p.Tyr475Cys)	not specified [RCV004375655]	uncertain significance	11	108719810	108719810	Human		name
405703943	CV3243601	single nucleotide variant	NM_004398.4(DDX10):c.1823C>T (p.Pro608Leu)	not specified [RCV004375657]	uncertain significance	11	108723320	108723320	Human		name
405703954	CV3243602	single nucleotide variant	NM_004398.4(DDX10):c.1831A>T (p.Ser611Cys)	not specified [RCV004375658]	uncertain significance	11	108723328	108723328	Human		name
405703962	CV3243603	single nucleotide variant	NM_004398.4(DDX10):c.1900G>A (p.Asp634Asn)	not specified [RCV004375659]	uncertain significance	11	108723397	108723397	Human		name
405703970	CV3243604	single nucleotide variant	NM_004398.4(DDX10):c.1933G>C (p.Gly645Arg)	not specified [RCV004375660]	uncertain significance	11	108723430	108723430	Human		name
405703976	CV3243605	single nucleotide variant	NM_004398.4(DDX10):c.1975C>A (p.Pro659Thr)	not specified [RCV004375661]	uncertain significance	11	108838455	108838455	Human		name
405703986	CV3243606	single nucleotide variant	NM_004398.4(DDX10):c.2257C>G (p.Leu753Val)	not specified [RCV004375662]	uncertain significance	11	108852162	108852162	Human		name
405703994	CV3243607	single nucleotide variant	NM_004398.4(DDX10):c.2332G>T (p.Asp778Tyr)	not specified [RCV004375663]	uncertain significance	11	108917900	108917900	Human		name
405703998	CV3243608	single nucleotide variant	NM_004398.4(DDX10):c.2615G>C (p.Arg872Thr)	not specified [RCV004375664]	uncertain significance	11	108940410	108940410	Human		name
407458419	CV3430477	single nucleotide variant	NM_004398.4(DDX10):c.1528G>A (p.Val510Ile)	not specified [RCV004611578]	likely benign	11	108723025	108723025	Human		name
407458428	CV3430480	single nucleotide variant	NM_004398.4(DDX10):c.1417G>A (p.Val473Ile)	not specified [RCV004611581]	uncertain significance	11	108719803	108719803	Human		name
407458433	CV3430482	single nucleotide variant	NM_004398.4(DDX10):c.1433C>G (p.Ser478Cys)	not specified [RCV004611583]	uncertain significance	11	108719819	108719819	Human		name
407458597	CV3430483	single nucleotide variant	NM_004398.4(DDX10):c.1193C>T (p.Thr398Ile)	not specified [RCV004611584]	uncertain significance	11	108693570	108693570	Human		name
407458440	CV3430484	single nucleotide variant	NM_004398.4(DDX10):c.2557C>A (p.Pro853Thr)	not specified [RCV004611585]	uncertain significance	11	108940352	108940352	Human		name
407458445	CV3430486	single nucleotide variant	NM_004398.4(DDX10):c.2167C>A (p.His723Asn)	not specified [RCV004611587]	uncertain significance	11	108841396	108841396	Human		name
407458448	CV3430487	single nucleotide variant	NM_004398.4(DDX10):c.2210A>C (p.Lys737Thr)	not specified [RCV004611588]	uncertain significance	11	108841439	108841439	Human		name
407458451	CV3430488	single nucleotide variant	NM_004398.4(DDX10):c.2348A>T (p.Asp783Val)	not specified [RCV004611589]	uncertain significance	11	108917916	108917916	Human		name
597805618	CV3661982	single nucleotide variant	NM_004398.4(DDX10):c.1402G>T (p.Ala468Ser)	not specified [RCV004908670]	uncertain significance	11	108715958	108715958	Human		name
597805619	CV3661983	single nucleotide variant	NM_004398.4(DDX10):c.1862C>T (p.Thr621Ile)	not specified [RCV004908671]	uncertain significance	11	108723359	108723359	Human		name
597805621	CV3661986	single nucleotide variant	NM_004398.4(DDX10):c.1612C>A (p.Pro538Thr)	not specified [RCV004908673]	uncertain significance	11	108723109	108723109	Human		name
597805622	CV3661987	single nucleotide variant	NM_004398.4(DDX10):c.1699G>A (p.Glu567Lys)	not specified [RCV004908674]	uncertain significance	11	108723196	108723196	Human		name
597805624	CV3661989	single nucleotide variant	NM_004398.4(DDX10):c.2288A>C (p.Asn763Thr)	not specified [RCV004908676]	uncertain significance	11	108852193	108852193	Human		name
597805625	CV3661990	single nucleotide variant	NM_004398.4(DDX10):c.2318A>G (p.Glu773Gly)	not specified [RCV004908677]	uncertain significance	11	108917886	108917886	Human		name
597805626	CV3661991	single nucleotide variant	NM_004398.4(DDX10):c.1733G>C (p.Gly578Ala)	not specified [RCV004908678]	uncertain significance	11	108723230	108723230	Human		name
597805627	CV3661992	single nucleotide variant	NM_004398.4(DDX10):c.2158A>T (p.Ile720Phe)	not specified [RCV004908679]	uncertain significance	11	108841387	108841387	Human		name
597805628	CV3661993	single nucleotide variant	NM_004398.4(DDX10):c.2185C>T (p.Leu729Phe)	not specified [RCV004908680]	uncertain significance	11	108841414	108841414	Human		name
597805629	CV3661995	single nucleotide variant	NM_004398.4(DDX10):c.2292G>C (p.Lys764Asn)	not specified [RCV004908681]	uncertain significance	11	108852197	108852197	Human		name
597805630	CV3661996	single nucleotide variant	NM_004398.4(DDX10):c.1927G>A (p.Val643Met)	not specified [RCV004908682]	uncertain significance	11	108723424	108723424	Human		name
597805631	CV3661997	single nucleotide variant	NM_004398.4(DDX10):c.1114A>G (p.Thr372Ala)	not specified [RCV004908683]	uncertain significance	11	108692014	108692014	Human		name
597805632	CV3661998	single nucleotide variant	NM_004398.4(DDX10):c.1039G>A (p.Gly347Ser)	not specified [RCV004908684]	uncertain significance	11	108691939	108691939	Human		name
597805633	CV3661999	single nucleotide variant	NM_004398.4(DDX10):c.1526G>A (p.Arg509His)	not specified [RCV004908685]	uncertain significance	11	108723023	108723023	Human		name
598263136	CV3959995	single nucleotide variant	NM_004398.4(DDX10):c.1652A>T (p.Tyr551Phe)	not specified [RCV005325595]	uncertain significance	11	108723149	108723149	Human		name
598263143	CV3959998	single nucleotide variant	NM_004398.4(DDX10):c.2540G>A (p.Arg847Lys)	not specified [RCV005325597]	likely benign	11	108940335	108940335	Human		name
598160581	CV3959999	single nucleotide variant	NM_004398.4(DDX10):c.1651T>C (p.Tyr551His)	not specified [RCV005328803]	uncertain significance	11	108723148	108723148	Human		name
598263150	CV3960001	single nucleotide variant	NM_004398.4(DDX10):c.2572C>G (p.Leu858Val)	not specified [RCV005325599]	uncertain significance	11	108940367	108940367	Human		name
598263153	CV3960002	single nucleotide variant	NM_004398.4(DDX10):c.1009C>T (p.Arg337Cys)	not specified [RCV005325600]	uncertain significance	11	108691909	108691909	Human		name
598263157	CV3960003	single nucleotide variant	NM_004398.4(DDX10):c.2366G>A (p.Gly789Glu)	not specified [RCV005325601]	uncertain significance	11	108917934	108917934	Human		name
598263160	CV3960004	single nucleotide variant	NM_004398.4(DDX10):c.2193A>C (p.Glu731Asp)	not specified [RCV005325602]	uncertain significance	11	108841422	108841422	Human		name
598263171	CV3960006	single nucleotide variant	NM_004398.4(DDX10):c.2266A>G (p.Arg756Gly)	not specified [RCV005325604]	uncertain significance	11	108852171	108852171	Human		name
598263178	CV3960008	single nucleotide variant	NM_004398.4(DDX10):c.2451T>A (p.Ser817Arg)	not specified [RCV005325606]	uncertain significance	11	108940246	108940246	Human		name
405273475	CV3192108	microsatellite	NM_004398.4(DDX10):c.1749AGA[3] (p.Glu586del)	DDX10-related disorder [RCV003914709]	likely benign	11	108723244	108723246	Human		name , trait , alternate_id

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