Morc3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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65 records found for search term Morc3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156294244	CV2306398	single nucleotide variant	NM_015358.3(MORC3):c.19C>G (p.Arg7Gly)	not specified [RCV004163092]	uncertain significance	21	36320283	36320283	Human		name
401920083	CV2824732	single nucleotide variant	NM_015358.3(MORC3):c.1284A>G (p.Gln428=)	not provided [RCV003431489]	likely benign	21	36360030	36360030	Human		name
405705058	CV3361921	single nucleotide variant	NM_015358.3(MORC3):c.109A>G (p.Ile37Val)	not specified [RCV004492909]	uncertain significance	21	36333715	36333715	Human		name
405704363	CV3361955	single nucleotide variant	NM_015358.3(MORC3):c.179A>G (p.His60Arg)	not specified [RCV004492943]	uncertain significance	21	36336940	36336940	Human		name
405704835	CV3362014	single nucleotide variant	NM_015358.3(MORC3):c.283G>A (p.Val95Ile)	not specified [RCV004493002]	uncertain significance	21	36337769	36337769	Human		name
597637059	CV3563882	single nucleotide variant	NM_015358.3(MORC3):c.203A>G (p.Asn68Ser)	not specified [RCV004824676]	uncertain significance	21	36336964	36336964	Human		name
15184763	CV705680	single nucleotide variant	NM_015358.3(MORC3):c.1884A>G (p.Ser628=)	not provided [RCV000952788]	benign	21	36369252	36369252	Human		name
156045261	CV2318995	single nucleotide variant	NM_015358.3(MORC3):c.343G>T (p.Ala115Ser)	not specified [RCV004178088]	uncertain significance	21	36337829	36337829	Human		name
156208806	CV2370035	single nucleotide variant	NM_015358.3(MORC3):c.385C>G (p.Leu129Val)	not specified [RCV004210932]	uncertain significance	21	36337871	36337871	Human		name
329401621	CV2457229	single nucleotide variant	NM_015358.3(MORC3):c.892A>G (p.Thr298Ala)	not specified [RCV004265300]	uncertain significance	21	36344918	36344918	Human		name
405704940	CV3362027	single nucleotide variant	NM_015358.3(MORC3):c.452A>G (p.Asn151Ser)	not specified [RCV004493015]	uncertain significance	21	36337938	36337938	Human		name
405704988	CV3362034	single nucleotide variant	NM_015358.3(MORC3):c.529A>G (p.Thr177Ala)	not specified [RCV004493022]	uncertain significance	21	36338842	36338842	Human		name
597637048	CV3563879	single nucleotide variant	NM_015358.3(MORC3):c.419C>T (p.Ala140Val)	not specified [RCV004824674]	uncertain significance	21	36337905	36337905	Human		name
597637065	CV3563888	single nucleotide variant	NM_015358.3(MORC3):c.373A>G (p.Met125Val)	not specified [RCV004824677]	uncertain significance	21	36337859	36337859	Human		name
597660323	CV3563892	single nucleotide variant	NM_015358.3(MORC3):c.349G>A (p.Val117Ile)	not specified [RCV004828360]	uncertain significance	21	36337835	36337835	Human		name
155969071	CV2213268	single nucleotide variant	NM_015358.3(MORC3):c.2146C>G (p.Gln716Glu)	not specified [RCV004085487]	uncertain significance	21	36369514	36369514	Human		name
155974186	CV2221021	single nucleotide variant	NM_015358.3(MORC3):c.1517A>G (p.Glu506Gly)	not specified [RCV004092702]	uncertain significance	21	36364157	36364157	Human		name
155973296	CV2224595	single nucleotide variant	NM_015358.3(MORC3):c.2815A>G (p.Thr939Ala)	not specified [RCV004098164]	uncertain significance	21	36375291	36375291	Human		name
155920932	CV2240441	single nucleotide variant	NM_015358.3(MORC3):c.1336T>G (p.Cys446Gly)	not specified [RCV004117330]	uncertain significance	21	36360188	36360188	Human		name
156148918	CV2265312	single nucleotide variant	NM_015358.3(MORC3):c.2656G>T (p.Asp886Tyr)	not specified [RCV004128204]	uncertain significance	21	36372521	36372521	Human		name
156045936	CV2268638	single nucleotide variant	NM_015358.3(MORC3):c.1366G>C (p.Asp456His)	not specified [RCV004124044]	uncertain significance	21	36360218	36360218	Human		name
155906858	CV2302103	single nucleotide variant	NM_015358.3(MORC3):c.1278G>A (p.Met426Ile)	not specified [RCV004159126]	likely benign	21	36360024	36360024	Human		name
156299792	CV2306886	single nucleotide variant	NM_015358.3(MORC3):c.2740C>A (p.Gln914Lys)	not specified [RCV004157414]	uncertain significance	21	36375216	36375216	Human		name
156395282	CV2325386	single nucleotide variant	NM_015358.3(MORC3):c.2267T>C (p.Leu756Pro)	not specified [RCV004177755]	uncertain significance	21	36369635	36369635	Human		name
156064572	CV2376001	single nucleotide variant	NM_015358.3(MORC3):c.1993G>A (p.Ala665Thr)	not specified [RCV004220249]	likely benign	21	36369361	36369361	Human		name
156269198	CV2379233	single nucleotide variant	NM_015358.3(MORC3):c.2359T>C (p.Cys787Arg)	not specified [RCV004223712]	uncertain significance	21	36369727	36369727	Human		name
329382466	CV2424477	single nucleotide variant	NM_015358.3(MORC3):c.2546C>T (p.Ser849Leu)	not specified [RCV004252367]	uncertain significance	21	36372411	36372411	Human		name
329375906	CV2441196	single nucleotide variant	NM_015358.3(MORC3):c.2318A>G (p.Tyr773Cys)	not specified [RCV004263592]	uncertain significance	21	36369686	36369686	Human		name
329351816	CV2455346	single nucleotide variant	NM_015358.3(MORC3):c.2272A>G (p.Ser758Gly)	not specified [RCV004274848]	uncertain significance	21	36369640	36369640	Human		name
329394267	CV2460685	single nucleotide variant	NM_015358.3(MORC3):c.1684C>G (p.Gln562Glu)	not specified [RCV004271033]	uncertain significance	21	36369052	36369052	Human		name
401740734	CV2679792	single nucleotide variant	NM_015358.3(MORC3):c.1642C>T (p.Arg548Cys)	not specified [RCV004282255]	uncertain significance	21	36369010	36369010	Human		name
401752644	CV2682889	single nucleotide variant	NM_015358.3(MORC3):c.1534C>T (p.His512Tyr)	not specified [RCV004283685]	uncertain significance	21	36364174	36364174	Human		name
401752648	CV2682890	single nucleotide variant	NM_015358.3(MORC3):c.2153A>T (p.His718Leu)	not specified [RCV004283686]	uncertain significance	21	36369521	36369521	Human		name
401742479	CV2697787	single nucleotide variant	NM_015358.3(MORC3):c.1535A>G (p.His512Arg)	not specified [RCV004300511]	uncertain significance	21	36364175	36364175	Human		name
401735716	CV2702854	single nucleotide variant	NM_015358.3(MORC3):c.2642C>T (p.Ser881Phe)	not specified [RCV004321199]	uncertain significance	21	36372507	36372507	Human		name
401722295	CV2706458	single nucleotide variant	NM_015358.3(MORC3):c.1888T>C (p.Ser630Pro)	not specified [RCV004317278]	uncertain significance	21	36369256	36369256	Human		name
401773270	CV2709218	single nucleotide variant	NM_015358.3(MORC3):c.1620C>G (p.Ser540Arg)	not specified [RCV004316389]	uncertain significance	21	36368988	36368988	Human		name
401740059	CV2709788	single nucleotide variant	NM_015358.3(MORC3):c.1577A>C (p.Asn526Thr)	not specified [RCV004320769]	uncertain significance	21	36364217	36364217	Human		name
405704572	CV3361923	single nucleotide variant	NM_015358.3(MORC3):c.1213C>T (p.Arg405Cys)	not specified [RCV004492911]	uncertain significance	21	36359959	36359959	Human		name
405704407	CV3361960	single nucleotide variant	NM_015358.3(MORC3):c.1807G>A (p.Val603Ile)	not specified [RCV004492948]	likely benign	21	36369175	36369175	Human		name
405704441	CV3361965	single nucleotide variant	NM_015358.3(MORC3):c.1853C>G (p.Pro618Arg)	not specified [RCV004492953]	uncertain significance	21	36369221	36369221	Human		name
405704536	CV3361977	single nucleotide variant	NM_015358.3(MORC3):c.2042C>A (p.Thr681Asn)	not specified [RCV004492965]	uncertain significance	21	36369410	36369410	Human		name
405704561	CV3361980	single nucleotide variant	NM_015358.3(MORC3):c.2056G>A (p.Asp686Asn)	not specified [RCV004492968]	uncertain significance	21	36369424	36369424	Human		name
405704630	CV3361989	single nucleotide variant	NM_015358.3(MORC3):c.2228C>T (p.Thr743Ile)	not specified [RCV004492977]	uncertain significance	21	36369596	36369596	Human		name
405704678	CV3361994	single nucleotide variant	NM_015358.3(MORC3):c.2399G>T (p.Cys800Phe)	not specified [RCV004492982]	uncertain significance	21	36369767	36369767	Human		name
405704778	CV3362006	single nucleotide variant	NM_015358.3(MORC3):c.2718T>G (p.Ile906Met)	not specified [RCV004492994]	uncertain significance	21	36375194	36375194	Human		name
407495906	CV3453858	single nucleotide variant	NM_015358.3(MORC3):c.2243C>T (p.Thr748Ile)	not specified [RCV004643335]	uncertain significance	21	36369611	36369611	Human		name
407495910	CV3453859	single nucleotide variant	NM_015358.3(MORC3):c.1972G>A (p.Glu658Lys)	not specified [RCV004643336]	uncertain significance	21	36369340	36369340	Human		name
407518946	CV3453860	single nucleotide variant	NM_015358.3(MORC3):c.2005C>T (p.Pro669Ser)	not specified [RCV004629060]	uncertain significance	21	36369373	36369373	Human		name
407518948	CV3453861	single nucleotide variant	NM_015358.3(MORC3):c.2305A>G (p.Met769Val)	not specified [RCV004629061]	likely benign	21	36369673	36369673	Human		name
407495916	CV3453862	single nucleotide variant	NM_015358.3(MORC3):c.1595C>A (p.Pro532His)	not specified [RCV004643337]	uncertain significance	21	36364235	36364235	Human		name
407495921	CV3453863	single nucleotide variant	NM_015358.3(MORC3):c.1806C>A (p.His602Gln)	not specified [RCV004643338]	uncertain significance	21	36369174	36369174	Human		name
597660274	CV3563878	single nucleotide variant	NM_015358.3(MORC3):c.1974G>C (p.Glu658Asp)	not specified [RCV004828351]	uncertain significance	21	36369342	36369342	Human		name
597660278	CV3563880	single nucleotide variant	NM_015358.3(MORC3):c.2464C>G (p.Gln822Glu)	not specified [RCV004828352]	uncertain significance	21	36369832	36369832	Human		name
597637054	CV3563881	single nucleotide variant	NM_015358.3(MORC3):c.1907A>G (p.Asn636Ser)	not specified [RCV004824675]	uncertain significance	21	36369275	36369275	Human		name
597660283	CV3563883	single nucleotide variant	NM_015358.3(MORC3):c.2387A>C (p.Glu796Ala)	not specified [RCV004828353]	uncertain significance	21	36369755	36369755	Human		name
597660288	CV3563884	single nucleotide variant	NM_015358.3(MORC3):c.2116G>C (p.Val706Leu)	not specified [RCV004828354]	uncertain significance	21	36369484	36369484	Human		name
597660294	CV3563885	single nucleotide variant	NM_015358.3(MORC3):c.2405A>G (p.Asn802Ser)	not specified [RCV004828355]	likely benign	21	36369773	36369773	Human		name
597660299	CV3563886	single nucleotide variant	NM_015358.3(MORC3):c.1643G>A (p.Arg548His)	not specified [RCV004828356]	uncertain significance	21	36369011	36369011	Human		name
597660304	CV3563887	single nucleotide variant	NM_015358.3(MORC3):c.1436C>T (p.Pro479Leu)	not specified [RCV004828357]	likely benign	21	36362212	36362212	Human		name
597660310	CV3563889	single nucleotide variant	NM_015358.3(MORC3):c.2632A>C (p.Ile878Leu)	not specified [RCV004828358]	uncertain significance	21	36372497	36372497	Human		name
597660315	CV3563890	single nucleotide variant	NM_015358.3(MORC3):c.1616A>G (p.Asn539Ser)	not specified [RCV004828359]	uncertain significance	21	36364256	36364256	Human		name
597637070	CV3563891	single nucleotide variant	NM_015358.3(MORC3):c.2278A>C (p.Asn760His)	not specified [RCV004824678]	uncertain significance	21	36369646	36369646	Human		name
598167952	CV3986280	single nucleotide variant	NM_015358.3(MORC3):c.2414G>C (p.Ser805Thr)	not specified [RCV005369615]	uncertain significance	21	36369782	36369782	Human		name
598201170	CV3986281	single nucleotide variant	NM_015358.3(MORC3):c.1841G>C (p.Gly614Ala)	not specified [RCV005375981]	uncertain significance	21	36369209	36369209	Human		name

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