Hdac10 Variant Search Result - Rat Genome Database

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78 records found for search term Hdac10

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155939490	CV2225540	single nucleotide variant	NM_032019.6(HDAC10):c.82C>A (p.Pro28Thr)	not specified [RCV004100922]	uncertain significance	22	50250883	50250883	Human		name
401775895	CV2724260	single nucleotide variant	NM_032019.6(HDAC10):c.35C>T (p.Thr12Met)	not specified [RCV004328139]	uncertain significance	22	50250998	50250998	Human		name
156341565	CV2225860	single nucleotide variant	NM_032019.6(HDAC10):c.158G>A (p.Arg53His)	not specified [RCV004103258]	uncertain significance	22	50250807	50250807	Human		name
156003397	CV2254176	single nucleotide variant	NM_032019.6(HDAC10):c.116G>A (p.Arg39Gln)	not specified [RCV004129858]	likely benign	22	50250849	50250849	Human		name
156291330	CV2324989	single nucleotide variant	NM_032019.6(HDAC10):c.241G>A (p.Glu81Lys)	not specified [RCV004175237]	uncertain significance	22	50250477	50250477	Human		name
156035743	CV2338957	single nucleotide variant	NM_032019.6(HDAC10):c.238A>G (p.Lys80Glu)	not specified [RCV004184546]	likely benign	22	50250480	50250480	Human		name
329390633	CV2437147	single nucleotide variant	NM_032019.6(HDAC10):c.289C>T (p.Pro97Ser)	not specified [RCV004262952]	uncertain significance	22	50250429	50250429	Human		name
401734883	CV2690703	single nucleotide variant	NM_032019.6(HDAC10):c.287A>G (p.His96Arg)	not specified [RCV004298432]	uncertain significance	22	50250431	50250431	Human		name
401864406	CV2773427	single nucleotide variant	NM_032019.6(HDAC10):c.229G>A (p.Val77Ile)	not specified [RCV004354067]	uncertain significance	22	50250489	50250489	Human		name
405790220	CV3266419	single nucleotide variant	NM_032019.6(HDAC10):c.136A>T (p.Arg46Trp)	not specified [RCV004399429]	uncertain significance	22	50250829	50250829	Human		name
405795947	CV3266423	single nucleotide variant	NM_032019.6(HDAC10):c.150G>T (p.Leu50Phe)	not specified [RCV004401415]	uncertain significance	22	50250815	50250815	Human		name
597781565	CV3679059	single nucleotide variant	NM_032019.6(HDAC10):c.227A>G (p.Gln76Arg)	not specified [RCV004930929]	uncertain significance	22	50250491	50250491	Human		name
597710368	CV3679069	single nucleotide variant	NM_032019.6(HDAC10):c.167C>T (p.Ser56Leu)	not specified [RCV004917449]	uncertain significance	22	50250798	50250798	Human		name
156243115	CV2246319	single nucleotide variant	NM_032019.6(HDAC10):c.854T>C (p.Leu285Pro)	not specified [RCV004107763]	uncertain significance	22	50248714	50248714	Human		name
156308206	CV2249480	single nucleotide variant	NM_032019.6(HDAC10):c.908G>A (p.Gly303Asp)	not specified [RCV004120529]	uncertain significance	22	50248471	50248471	Human		name
156270471	CV2315535	single nucleotide variant	NM_032019.6(HDAC10):c.610C>A (p.Pro204Thr)	not specified [RCV004169582]	uncertain significance	22	50249408	50249408	Human		name
156057396	CV2343542	single nucleotide variant	NM_032019.6(HDAC10):c.685A>C (p.Asn229His)	not specified [RCV004190576]	uncertain significance	22	50249333	50249333	Human		name
156183179	CV2353212	single nucleotide variant	NM_032019.6(HDAC10):c.899T>C (p.Val300Ala)	not specified [RCV004203680]	uncertain significance	22	50248669	50248669	Human		name
156169654	CV2354805	single nucleotide variant	NM_032019.6(HDAC10):c.308C>T (p.Ala103Val)	not specified [RCV004198332]	uncertain significance	22	50250144	50250144	Human		name
155927194	CV2365890	single nucleotide variant	NM_032019.6(HDAC10):c.397G>A (p.Gly133Arg)	not specified [RCV004214419]	uncertain significance	22	50249957	50249957	Human		name
329394108	CV2450085	single nucleotide variant	NM_032019.6(HDAC10):c.469G>A (p.Ala157Thr)	not specified [RCV004269131]	uncertain significance	22	50249885	50249885	Human		name
401736563	CV2683053	single nucleotide variant	NM_032019.6(HDAC10):c.730C>T (p.His244Tyr)	not specified [RCV004283830]	uncertain significance	22	50249129	50249129	Human		name
401856217	CV2761320	single nucleotide variant	NM_032019.6(HDAC10):c.782C>T (p.Ser261Leu)	not specified [RCV004341187]	uncertain significance	22	50248865	50248865	Human		name
401899027	CV2785958	single nucleotide variant	NM_032019.6(HDAC10):c.614T>C (p.Phe205Ser)	not specified [RCV004359802]	uncertain significance	22	50249404	50249404	Human		name
405795959	CV3266427	single nucleotide variant	NM_032019.6(HDAC10):c.448G>A (p.Val150Met)	not specified [RCV004401419]	uncertain significance	22	50249906	50249906	Human		name
405795966	CV3266429	single nucleotide variant	NM_032019.6(HDAC10):c.646C>T (p.Arg216Trp)	not specified [RCV004401421]	uncertain significance	22	50249372	50249372	Human		name
405795969	CV3266430	single nucleotide variant	NM_032019.6(HDAC10):c.797C>T (p.Ser266Leu)	not specified [RCV004401422]	uncertain significance	22	50248850	50248850	Human		name
405795972	CV3266431	single nucleotide variant	NM_032019.6(HDAC10):c.946A>C (p.Met316Leu)	not specified [RCV004401423]	uncertain significance	22	50248433	50248433	Human		name
405795975	CV3266432	single nucleotide variant	NM_032019.6(HDAC10):c.983C>G (p.Pro328Arg)	not specified [RCV004401424]	uncertain significance	22	50248396	50248396	Human		name
407514416	CV3440216	single nucleotide variant	NM_032019.6(HDAC10):c.977C>T (p.Ala326Val)	not specified [RCV004627601]	uncertain significance	22	50248402	50248402	Human		name
597710293	CV3679056	single nucleotide variant	NM_032019.6(HDAC10):c.875T>C (p.Leu292Pro)	not specified [RCV004917441]	uncertain significance	22	50248693	50248693	Human		name
597710302	CV3679057	single nucleotide variant	NM_032019.6(HDAC10):c.427G>A (p.Gly143Arg)	not specified [RCV004917442]	uncertain significance	22	50249927	50249927	Human		name
597710311	CV3679058	single nucleotide variant	NM_032019.6(HDAC10):c.565G>A (p.Val189Ile)	not specified [RCV004917443]	uncertain significance	22	50249453	50249453	Human		name
597781575	CV3679063	single nucleotide variant	NM_032019.6(HDAC10):c.616C>G (p.Leu206Val)	not specified [RCV004930931]	uncertain significance	22	50249402	50249402	Human		name
597710343	CV3679065	single nucleotide variant	NM_032019.6(HDAC10):c.520C>T (p.His174Tyr)	not specified [RCV004917446]	uncertain significance	22	50249678	50249678	Human		name
597781579	CV3679066	single nucleotide variant	NM_032019.6(HDAC10):c.835C>A (p.Pro279Thr)	not specified [RCV004930932]	uncertain significance	22	50248733	50248733	Human		name
597710383	CV3679071	single nucleotide variant	NM_032019.6(HDAC10):c.310C>T (p.Arg104Trp)	not specified [RCV004917451]	uncertain significance	22	50250142	50250142	Human		name
598266232	CV3971632	single nucleotide variant	NM_032019.6(HDAC10):c.715G>A (p.Val239Met)	not specified [RCV005349231]	uncertain significance	22	50249144	50249144	Human		name
598266240	CV3971634	single nucleotide variant	NM_032019.6(HDAC10):c.490C>T (p.His164Tyr)	not specified [RCV005349233]	uncertain significance	22	50249864	50249864	Human		name
598266243	CV3971635	single nucleotide variant	NM_032019.6(HDAC10):c.838G>C (p.Glu280Gln)	not specified [RCV005349234]	uncertain significance	22	50248730	50248730	Human		name
156366328	CV2203305	single nucleotide variant	NM_032019.6(HDAC10):c.1605G>C (p.Glu535Asp)	not specified [RCV004071336]	uncertain significance	22	50246343	50246343	Human		name
156400948	CV2213626	single nucleotide variant	NM_032019.6(HDAC10):c.1016C>T (p.Ala339Val)	not specified [RCV004089710]	uncertain significance	22	50248290	50248290	Human		name
155907783	CV2302288	single nucleotide variant	NM_032019.6(HDAC10):c.1072C>G (p.Gln358Glu)	not specified [RCV004161054]	uncertain significance	22	50248234	50248234	Human		name
156055224	CV2320519	single nucleotide variant	NM_032019.6(HDAC10):c.1987T>C (p.Cys663Arg)	not specified [RCV004172149]	uncertain significance	22	50245530	50245530	Human		name
156277169	CV2328161	single nucleotide variant	NM_032019.6(HDAC10):c.1726C>G (p.Leu576Val)	not specified [RCV004173260]	uncertain significance	22	50246017	50246017	Human		name
156278304	CV2328449	single nucleotide variant	NM_032019.6(HDAC10):c.1748A>G (p.His583Arg)	not specified [RCV004175545]	uncertain significance	22	50245995	50245995	Human		name
156035734	CV2338956	single nucleotide variant	NM_032019.6(HDAC10):c.1462G>A (p.Ala488Thr)	not specified [RCV004184545]	uncertain significance	22	50246927	50246927	Human		name
156146581	CV2357944	single nucleotide variant	NM_032019.6(HDAC10):c.1232G>T (p.Arg411Leu)	not specified [RCV004209727]	uncertain significance	22	50247995	50247995	Human		name
329373088	CV2434101	single nucleotide variant	NM_032019.6(HDAC10):c.1546C>T (p.Arg516Trp)	not specified [RCV004249999]	uncertain significance	22	50246704	50246704	Human		name
329373555	CV2434531	single nucleotide variant	NM_032019.6(HDAC10):c.1055C>T (p.Pro352Leu)	not specified [RCV004254234]	uncertain significance	22	50248251	50248251	Human		name
329367126	CV2442117	single nucleotide variant	NM_032019.6(HDAC10):c.1792C>T (p.Arg598Trp)	not specified [RCV004264313]	uncertain significance	22	50245951	50245951	Human		name
401742774	CV2673870	single nucleotide variant	NM_032019.6(HDAC10):c.1575G>T (p.Arg525Ser)	not specified [RCV004293250]	uncertain significance	22	50246373	50246373	Human		name
401742778	CV2673871	single nucleotide variant	NM_032019.6(HDAC10):c.1576A>C (p.Ser526Arg)	not specified [RCV004293251]	uncertain significance	22	50246372	50246372	Human		name
401758538	CV2700576	single nucleotide variant	NM_032019.6(HDAC10):c.1639C>G (p.Pro547Ala)	not specified [RCV004313312]	uncertain significance	22	50246309	50246309	Human		name
401770283	CV2711046	single nucleotide variant	NM_032019.6(HDAC10):c.1963G>C (p.Glu655Gln)	not specified [RCV004310742]	uncertain significance	22	50245698	50245698	Human		name
401782940	CV2716053	single nucleotide variant	NM_032019.6(HDAC10):c.1597G>A (p.Gly533Ser)	not specified [RCV004323302]	uncertain significance	22	50246351	50246351	Human		name
401879650	CV2755219	single nucleotide variant	NM_032019.6(HDAC10):c.1147C>A (p.Pro383Thr)	not specified [RCV004337408]	uncertain significance	22	50248080	50248080	Human		name
401864414	CV2777834	single nucleotide variant	NM_032019.6(HDAC10):c.1018C>G (p.Leu340Val)	not specified [RCV004346021]	uncertain significance	22	50248288	50248288	Human		name
401886454	CV2780365	single nucleotide variant	NM_032019.6(HDAC10):c.1256C>G (p.Pro419Arg)	not specified [RCV004357767]	uncertain significance	22	50247971	50247971	Human		name
401876595	CV2782975	single nucleotide variant	NM_032019.6(HDAC10):c.1265C>A (p.Thr422Lys)	not specified [RCV004361766]	uncertain significance	22	50247962	50247962	Human		name
401876599	CV2782976	single nucleotide variant	NM_032019.6(HDAC10):c.1612G>C (p.Ala538Pro)	not specified [RCV004361767]	uncertain significance	22	50246336	50246336	Human		name
405790215	CV3266417	single nucleotide variant	NM_032019.6(HDAC10):c.1153G>C (p.Gly385Arg)	not specified [RCV004399427]	uncertain significance	22	50248074	50248074	Human		name
405790217	CV3266418	single nucleotide variant	NM_032019.6(HDAC10):c.1289T>C (p.Ile430Thr)	not specified [RCV004399428]	uncertain significance	22	50247938	50247938	Human		name
405790223	CV3266420	single nucleotide variant	NM_032019.6(HDAC10):c.1384A>G (p.Lys462Glu)	not specified [RCV004399430]	uncertain significance	22	50247730	50247730	Human		name
405795944	CV3266422	single nucleotide variant	NM_032019.6(HDAC10):c.1466C>A (p.Ala489Asp)	not specified [RCV004401414]	uncertain significance	22	50246923	50246923	Human		name
405795950	CV3266424	single nucleotide variant	NM_032019.6(HDAC10):c.1541T>C (p.Leu514Pro)	not specified [RCV004401416]	uncertain significance	22	50246709	50246709	Human		name
405795956	CV3266426	single nucleotide variant	NM_032019.6(HDAC10):c.1774C>T (p.Leu592Phe)	not specified [RCV004401418]	uncertain significance	22	50245969	50245969	Human		name
407514419	CV3440217	single nucleotide variant	NM_032019.6(HDAC10):c.1408A>G (p.Met470Val)	not specified [RCV004627602]	uncertain significance	22	50247706	50247706	Human		name
407514421	CV3440218	single nucleotide variant	NM_032019.6(HDAC10):c.1219G>A (p.Ala407Thr)	not specified [RCV004627603]	likely benign	22	50248008	50248008	Human		name
597710285	CV3679055	single nucleotide variant	NM_032019.6(HDAC10):c.1043C>T (p.Ala348Val)	not specified [RCV004917440]	uncertain significance	22	50248263	50248263	Human		name
597781569	CV3679060	single nucleotide variant	NM_032019.6(HDAC10):c.1838C>G (p.Ser613Cys)	not specified [RCV004930930]	uncertain significance	22	50245823	50245823	Human		name
597710332	CV3679064	single nucleotide variant	NM_032019.6(HDAC10):c.1555G>C (p.Asp519His)	not specified [RCV004917445]	uncertain significance	22	50246695	50246695	Human		name
597710351	CV3679067	single nucleotide variant	NM_032019.6(HDAC10):c.1561G>A (p.Ala521Thr)	not specified [RCV004917447]	uncertain significance	22	50246689	50246689	Human		name
597710359	CV3679068	single nucleotide variant	NM_032019.6(HDAC10):c.1894A>G (p.Ser632Gly)	not specified [RCV004917448]	uncertain significance	22	50245767	50245767	Human		name
597710376	CV3679070	single nucleotide variant	NM_032019.6(HDAC10):c.1922C>T (p.Pro641Leu)	not specified [RCV004917450]	uncertain significance	22	50245739	50245739	Human		name
597781583	CV3679072	single nucleotide variant	NM_032019.6(HDAC10):c.1178C>A (p.Ser393Tyr)	not specified [RCV004930933]	uncertain significance	22	50248049	50248049	Human		name
598266227	CV3971631	single nucleotide variant	NM_032019.6(HDAC10):c.1763C>T (p.Pro588Leu)	not specified [RCV005349230]	uncertain significance	22	50245980	50245980	Human		name
598266236	CV3971633	single nucleotide variant	NM_032019.6(HDAC10):c.1507G>A (p.Ala503Thr)	not specified [RCV005349232]	uncertain significance	22	50246882	50246882	Human		name

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