Mgrn1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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82 records found for search term Mgrn1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15150190	CV760482	single nucleotide variant	NM_015246.4(MGRN1):c.1618+9C>G	not provided [RCV000923427]	likely benign	16	4683941	4683941	Human		name
15196332	CV760439	single nucleotide variant	NM_015246.4(MGRN1):c.1618+10T>G	not provided [RCV000911666]	likely benign	16	4683942	4683942	Human		name
156010188	CV2290984	single nucleotide variant	NM_015246.4(MGRN1):c.7T>A (p.Ser3Thr)	not specified [RCV004151535]	uncertain significance	16	4624967	4624967	Human		name
15123990	CV714918	single nucleotide variant	NM_015246.4(MGRN1):c.141C>A (p.Pro47=)	not provided [RCV000963341]	benign	16	4650417	4650417	Human		name
401911463	CV2811035	single nucleotide variant	NM_015246.4(MGRN1):c.657G>C (p.Val219=)	not provided [RCV003426567]	likely benign	16	4665130	4665130	Human		name
401938500	CV2811036	single nucleotide variant	NM_015246.4(MGRN1):c.849C>T (p.Ser283=)	not provided [RCV003417621]	likely benign	16	4673551	4673551	Human		name
156320669	CV2197367	single nucleotide variant	NM_015246.4(MGRN1):c.137C>T (p.Thr46Ile)	not specified [RCV004081109]	uncertain significance	16	4650413	4650413	Human		name
329390397	CV2450261	single nucleotide variant	NM_015246.4(MGRN1):c.172A>G (p.Met58Val)	not specified [RCV004271360]	uncertain significance	16	4650448	4650448	Human		name
401736643	CV2683072	single nucleotide variant	NM_015246.4(MGRN1):c.232C>A (p.His78Asn)	not specified [RCV004283847]	uncertain significance	16	4651987	4651987	Human		name
401745368	CV2693241	single nucleotide variant	NM_015246.4(MGRN1):c.248C>T (p.Thr83Met)	not specified [RCV004295214]	uncertain significance	16	4652003	4652003	Human		name
401744299	CV2696976	single nucleotide variant	NM_015246.4(MGRN1):c.272G>A (p.Arg91His)	not specified [RCV004292968]	uncertain significance	16	4652027	4652027	Human		name
401884258	CV2789630	single nucleotide variant	NM_015246.4(MGRN1):c.190G>A (p.Gly64Ser)	not specified [RCV004360230]	uncertain significance	16	4650466	4650466	Human		name
401938501	CV2811037	single nucleotide variant	NM_015246.4(MGRN1):c.1713C>T (p.Ala571=)	not provided [RCV003417622]	likely benign	16	4688890	4688890	Human		name
597635523	CV3563397	single nucleotide variant	NM_015246.4(MGRN1):c.210T>G (p.Phe70Leu)	not specified [RCV004824358]	uncertain significance	16	4651965	4651965	Human		name
598253587	CV3982403	single nucleotide variant	NM_015246.4(MGRN1):c.104C>T (p.Ser35Leu)	not specified [RCV005367067]	uncertain significance	16	4650380	4650380	Human		name
15112780	CV755187	single nucleotide variant	NM_015246.4(MGRN1):c.1413C>T (p.Ser471=)	not provided [RCV000916976]	likely benign	16	4682877	4682877	Human		name
156265856	CV2198695	single nucleotide variant	NM_015246.4(MGRN1):c.385C>T (p.Arg129Cys)	not specified [RCV004075705]	uncertain significance	16	4652766	4652766	Human		name
156116426	CV2209084	single nucleotide variant	NM_015246.4(MGRN1):c.439G>A (p.Ala147Thr)	not specified [RCV004093316]	uncertain significance	16	4652820	4652820	Human		name
156231248	CV2227585	single nucleotide variant	NM_015246.4(MGRN1):c.625G>A (p.Asp209Asn)	not specified [RCV004094008]	uncertain significance	16	4664772	4664772	Human		name
156293257	CV2233527	single nucleotide variant	NM_015246.4(MGRN1):c.688G>A (p.Gly230Ser)	not specified [RCV004100007]	uncertain significance	16	4668274	4668274	Human		name
155993535	CV2253594	single nucleotide variant	NM_015246.4(MGRN1):c.479C>G (p.Thr160Ser)	not specified [RCV004125282]	uncertain significance	16	4657281	4657281	Human		name
156356500	CV2257426	single nucleotide variant	NM_015246.4(MGRN1):c.481G>A (p.Val161Ile)	not specified [RCV004125507]	uncertain significance	16	4657283	4657283	Human		name
156016097	CV2270137	single nucleotide variant	NM_015246.4(MGRN1):c.580C>G (p.Arg194Gly)	not specified [RCV004129084]	uncertain significance	16	4664727	4664727	Human		name
156366443	CV2272299	single nucleotide variant	NM_015246.4(MGRN1):c.488A>G (p.Tyr163Cys)	not specified [RCV004126960]	uncertain significance	16	4657290	4657290	Human		name
156232207	CV2273662	single nucleotide variant	NM_015246.4(MGRN1):c.313G>A (p.Asp105Asn)	not specified [RCV004132326]	uncertain significance	16	4652694	4652694	Human		name
156061257	CV2280369	single nucleotide variant	NM_015246.4(MGRN1):c.455A>G (p.Lys152Arg)	not specified [RCV004140555]	uncertain significance	16	4657257	4657257	Human		name
156340717	CV2348023	single nucleotide variant	NM_015246.4(MGRN1):c.376G>A (p.Ala126Thr)	not specified [RCV004197705]	uncertain significance	16	4652757	4652757	Human		name
401724342	CV2681389	single nucleotide variant	NM_015246.4(MGRN1):c.988C>T (p.Arg330Trp)	not specified [RCV004291934]	uncertain significance	16	4677495	4677495	Human		name
401857569	CV2760250	single nucleotide variant	NM_015246.4(MGRN1):c.379G>A (p.Asp127Asn)	not specified [RCV004347419]	uncertain significance	16	4652760	4652760	Human		name
405661009	CV3289184	single nucleotide variant	NM_015246.4(MGRN1):c.386G>A (p.Arg129His)	not specified [RCV004417305]	uncertain significance	16	4652767	4652767	Human		name
405661014	CV3289186	single nucleotide variant	NM_015246.4(MGRN1):c.586G>A (p.Val196Met)	not specified [RCV004417307]	uncertain significance	16	4664733	4664733	Human		name
405661017	CV3289187	single nucleotide variant	NM_015246.4(MGRN1):c.796C>T (p.Pro266Ser)	not specified [RCV004417308]	uncertain significance	16	4673498	4673498	Human		name
407503762	CV3446791	single nucleotide variant	NM_015246.4(MGRN1):c.649G>A (p.Ala217Thr)	not specified [RCV004645579]	uncertain significance	16	4665122	4665122	Human		name
597635529	CV3563402	single nucleotide variant	NM_015246.4(MGRN1):c.416C>T (p.Ser139Leu)	not specified [RCV004824359]	uncertain significance	16	4652797	4652797	Human		name
597635538	CV3563408	single nucleotide variant	NM_015246.4(MGRN1):c.613G>A (p.Val205Met)	not specified [RCV004824361]	uncertain significance	16	4664760	4664760	Human		name
597644975	CV3563410	single nucleotide variant	NM_015246.4(MGRN1):c.308A>C (p.Asp103Ala)	not specified [RCV004832867]	uncertain significance	16	4652689	4652689	Human		name
598253551	CV3982396	single nucleotide variant	NM_015246.4(MGRN1):c.733C>T (p.Arg245Trp)	not specified [RCV005367062]	uncertain significance	16	4671397	4671397	Human		name
598253560	CV3982397	single nucleotide variant	NM_015246.4(MGRN1):c.509A>T (p.Gln170Leu)	not specified [RCV005367063]	uncertain significance	16	4657311	4657311	Human		name
598185503	CV3982399	single nucleotide variant	NM_015246.4(MGRN1):c.559G>A (p.Glu187Lys)	not specified [RCV005373263]	uncertain significance	16	4657361	4657361	Human		name
598253595	CV3982404	single nucleotide variant	NM_015246.4(MGRN1):c.350T>C (p.Leu117Pro)	not specified [RCV005367068]	uncertain significance	16	4652731	4652731	Human		name
155920677	CV2210863	single nucleotide variant	NM_015246.4(MGRN1):c.1331G>A (p.Gly444Asp)	not specified [RCV004085949]	uncertain significance	16	4681749	4681749	Human		name
156160478	CV2262670	single nucleotide variant	NM_015246.4(MGRN1):c.1642G>A (p.Ala548Thr)	not specified [RCV004130864]	uncertain significance	16	4688819	4688819	Human		name
156147047	CV2289318	single nucleotide variant	NM_015246.4(MGRN1):c.1259C>T (p.Ser420Leu)	not specified [RCV004152293]	uncertain significance	16	4681677	4681677	Human		name
155932242	CV2364359	single nucleotide variant	NM_015246.4(MGRN1):c.1666C>T (p.Pro556Ser)	not specified [RCV004223577]	uncertain significance	16	4688843	4688843	Human		name
156207892	CV2382429	single nucleotide variant	NM_015246.4(MGRN1):c.1337C>T (p.Pro446Leu)	not specified [RCV004230768]	uncertain significance	16	4681755	4681755	Human		name
329376157	CV2437999	single nucleotide variant	NM_015246.4(MGRN1):c.1621C>T (p.Arg541Trp)	not specified [RCV004263710]	likely benign	16	4688798	4688798	Human		name
329358198	CV2450215	single nucleotide variant	NM_015246.4(MGRN1):c.1087C>G (p.Pro363Ala)	not specified [RCV004271322]	uncertain significance	16	4680053	4680053	Human		name
329402734	CV2451301	single nucleotide variant	NM_015246.4(MGRN1):c.1547T>C (p.Ile516Thr)	not specified [RCV004271995]	uncertain significance	16	4683861	4683861	Human		name
329397112	CV2456606	single nucleotide variant	NM_015246.4(MGRN1):c.1367G>A (p.Arg456Gln)	not specified [RCV004277797]	uncertain significance	16	4682831	4682831	Human		name
329398017	CV2466549	single nucleotide variant	NM_015246.4(MGRN1):c.1300G>A (p.Asp434Asn)	not specified [RCV004274086]	uncertain significance	16	4681718	4681718	Human		name
401726773	CV2674538	single nucleotide variant	NM_015246.4(MGRN1):c.1330G>T (p.Gly444Cys)	not specified [RCV004291416]	uncertain significance	16	4681748	4681748	Human		name
401756701	CV2696436	single nucleotide variant	NM_015246.4(MGRN1):c.1096G>A (p.Ala366Thr)	not specified [RCV004312520]	uncertain significance	16	4680062	4680062	Human		name
401750507	CV2715662	single nucleotide variant	NM_015246.4(MGRN1):c.1253G>C (p.Gly418Ala)	not specified [RCV004327038]	uncertain significance	16	4681671	4681671	Human		name
401767170	CV2730852	single nucleotide variant	NM_015246.4(MGRN1):c.1183C>G (p.Leu395Val)	not specified [RCV004331647]	uncertain significance	16	4681601	4681601	Human		name
401887708	CV2772105	single nucleotide variant	NM_015246.4(MGRN1):c.1699G>C (p.Asp567His)	not specified [RCV004344760]	uncertain significance	16	4688876	4688876	Human		name
405660984	CV3289175	single nucleotide variant	NM_015246.4(MGRN1):c.1030G>A (p.Val344Ile)	not specified [RCV004417296]	uncertain significance	16	4677537	4677537	Human		name
405660986	CV3289176	single nucleotide variant	NM_015246.4(MGRN1):c.1147C>G (p.Pro383Ala)	not specified [RCV004417297]	uncertain significance	16	4681565	4681565	Human		name
405660989	CV3289177	single nucleotide variant	NM_015246.4(MGRN1):c.1226C>T (p.Pro409Leu)	not specified [RCV004417298]	uncertain significance	16	4681644	4681644	Human		name
405660996	CV3289179	single nucleotide variant	NM_015246.4(MGRN1):c.1361C>A (p.Thr454Asn)	not specified [RCV004417300]	uncertain significance	16	4682825	4682825	Human		name
405660997	CV3289180	single nucleotide variant	NM_015246.4(MGRN1):c.1643C>A (p.Ala548Asp)	not specified [RCV004417301]	uncertain significance	16	4688820	4688820	Human		name
405661000	CV3289181	single nucleotide variant	NM_015246.4(MGRN1):c.1654G>A (p.Ala552Thr)	not specified [RCV004417302]	uncertain significance	16	4688831	4688831	Human		name
405661002	CV3289182	single nucleotide variant	NM_015246.4(MGRN1):c.1670C>T (p.Thr557Ile)	not specified [RCV004417303]	uncertain significance	16	4688847	4688847	Human		name
407503755	CV3446789	single nucleotide variant	NM_015246.4(MGRN1):c.1435C>A (p.Pro479Thr)	not specified [RCV004645577]	uncertain significance	16	4682899	4682899	Human		name
407503759	CV3446790	single nucleotide variant	NM_015246.4(MGRN1):c.1546A>G (p.Ile516Val)	not specified [RCV004645578]	uncertain significance	16	4683860	4683860	Human		name
407503766	CV3446792	single nucleotide variant	NM_015246.4(MGRN1):c.1427C>T (p.Ala476Val)	not specified [RCV004645580]	uncertain significance	16	4682891	4682891	Human		name
407518382	CV3446793	single nucleotide variant	NM_015246.4(MGRN1):c.1601C>T (p.Ala534Val)	not specified [RCV004628851]	uncertain significance	16	4683915	4683915	Human		name
597644920	CV3563398	single nucleotide variant	NM_015246.4(MGRN1):c.1714G>A (p.Glu572Lys)	not specified [RCV004832859]	uncertain significance	16	4688891	4688891	Human		name
597644927	CV3563399	single nucleotide variant	NM_015246.4(MGRN1):c.1576G>A (p.Glu526Lys)	not specified [RCV004832860]	uncertain significance	16	4683890	4683890	Human		name
597644933	CV3563400	single nucleotide variant	NM_015246.4(MGRN1):c.1711G>A (p.Ala571Thr)	not specified [RCV004832861]	likely benign	16	4688888	4688888	Human		name
597644940	CV3563401	single nucleotide variant	NM_015246.4(MGRN1):c.1208C>T (p.Pro403Leu)	not specified [RCV004832862]	uncertain significance	16	4681626	4681626	Human		name
597644947	CV3563403	single nucleotide variant	NM_015246.4(MGRN1):c.1163C>T (p.Pro388Leu)	not specified [RCV004832863]	uncertain significance	16	4681581	4681581	Human		name
597644955	CV3563404	single nucleotide variant	NM_015246.4(MGRN1):c.1356C>G (p.Asp452Glu)	not specified [RCV004832864]	uncertain significance	16	4681774	4681774	Human		name
597644961	CV3563405	single nucleotide variant	NM_015246.4(MGRN1):c.1535G>C (p.Arg512Pro)	not specified [RCV004832865]	uncertain significance	16	4683849	4683849	Human		name
597635534	CV3563406	single nucleotide variant	NM_015246.4(MGRN1):c.1282T>C (p.Cys428Arg)	not specified [RCV004824360]	uncertain significance	16	4681700	4681700	Human		name
597644969	CV3563409	single nucleotide variant	NM_015246.4(MGRN1):c.1631C>T (p.Ser544Phe)	not specified [RCV004832866]	uncertain significance	16	4688808	4688808	Human		name
598185498	CV3982398	single nucleotide variant	NM_015246.4(MGRN1):c.1261G>C (p.Asp421His)	not specified [RCV005373262]	uncertain significance	16	4681679	4681679	Human		name
598253580	CV3982402	single nucleotide variant	NM_015246.4(MGRN1):c.1015G>A (p.Val339Met)	not specified [RCV005367066]	uncertain significance	16	4677522	4677522	Human		name
598185508	CV3982405	single nucleotide variant	NM_015246.4(MGRN1):c.1307T>C (p.Ile436Thr)	not specified [RCV005373264]	uncertain significance	16	4681725	4681725	Human		name
598253602	CV3982406	single nucleotide variant	NM_015246.4(MGRN1):c.1334G>C (p.Arg445Thr)	not specified [RCV005367069]	uncertain significance	16	4681752	4681752	Human		name
598185514	CV3982407	single nucleotide variant	NM_015246.4(MGRN1):c.1675C>T (p.Pro559Ser)	not specified [RCV005373265]	uncertain significance	16	4688852	4688852	Human		name
598185519	CV3982408	single nucleotide variant	NM_015246.4(MGRN1):c.1639A>G (p.Thr547Ala)	not specified [RCV005373266]	uncertain significance	16	4688816	4688816	Human		name
8627819	CV82963	single nucleotide variant	NM_001142289.2(MGRN1):c.1366C>T (p.Pro456Ser)	Malignant melanoma [RCV000063043]	not provided	16	4682896	4682896	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
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