Gnrh1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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44 records found for search term Gnrh1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
28907575	CV899382	single nucleotide variant	NM_000825.3(GNRH1):c.-984C>G	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV001159619]	uncertain significance	8	25424326	25424326	Human	1	name
11652601	CV308722	deletion	NM_000825.3(GNRH1):c.-1015del	Isolated GnRH Deficiency [RCV000305814]	uncertain significance	8	25424357	25424357	Human	1	name
11635819	CV308723	duplication	NM_000825.3(GNRH1):c.-1015dup	Isolated GnRH Deficiency [RCV000400073]	likely benign	8	25424356	25424357	Human	1	name
28907578	CV899383	single nucleotide variant	NM_000825.3(GNRH1):c.-1198G>A	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV001159620]	uncertain significance	8	25424540	25424540	Human	1	name
28909953	CV899384	single nucleotide variant	NM_000825.3(GNRH1):c.-1316C>T	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV001161004]	uncertain significance	8	25424658	25424658	Human	1	name
28909955	CV899385	single nucleotide variant	NM_000825.3(GNRH1):c.-1624G>A	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV001161005]	uncertain significance	8	25424966	25424966	Human	1	name
11606828	CV305012	single nucleotide variant	NM_001083111.2(GNRH1):c.-2+5A>C	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV000336141]	likely benign\|uncertain significance	8	25424196	25424196	Human	1	name
597872237	CV3849459	single nucleotide variant	NM_001083111.2(GNRH1):c.-1-5C>T	not provided [RCV005197640]	uncertain significance	8	25423336	25423336	Human		name
11608267	CV305011	single nucleotide variant	NM_001083111.2(GNRH1):c.-1-29T>C	Isolated GnRH Deficiency [RCV000352875]	uncertain significance	8	25423360	25423360	Human	1	name
11606179	CV313851	single nucleotide variant	NM_001083111.2(GNRH1):c.237+8A>C	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV000328353]\|not provided [RCV003727719]	likely benign\|uncertain significance	8	25421565	25421565	Human	1	name
28907573	CV899381	single nucleotide variant	NM_001083111.2(GNRH1):c.-2+59G>T	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV001159618]	uncertain significance	8	25424142	25424142	Human	1	name
150468211	CV1218883	single nucleotide variant	NM_001083111.2(GNRH1):c.141+40T>G	not provided [RCV001614635]	benign	8	25423150	25423150	Human		name
150483509	CV1245123	single nucleotide variant	NM_001083111.2(GNRH1):c.141+85A>G	not provided [RCV001653300]	benign	8	25423105	25423105	Human		name
11611899	CV308710	single nucleotide variant	NM_001083111.2(GNRH1):c.-2+388T>C	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV000400342]\|not provided [RCV004705465]	likely benign\|uncertain significance	8	25423813	25423813	Human	1	name
11603401	CV308720	single nucleotide variant	NM_001083111.2(GNRH1):c.-2+194C>A	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV000299783]	uncertain significance	8	25424007	25424007	Human	1	name
11602591	CV313849	single nucleotide variant	NM_001083111.2(GNRH1):c.238-12T>C	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV000292033]	uncertain significance	8	25419472	25419472	Human	1	name
11658505	CV313876	single nucleotide variant	NM_001083111.2(GNRH1):c.-1-148G>A	Isolated GnRH Deficiency [RCV000349298]	uncertain significance	8	25423479	25423479	Human	1	name
11663295	CV313939	single nucleotide variant	NM_001083111.2(GNRH1):c.-1-110A>G	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV000394363]	uncertain significance	8	25423441	25423441	Human	1	name
11650704	CV313941	single nucleotide variant	NM_001083111.2(GNRH1):c.-1-140G>A	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV000294346]	uncertain significance	8	25423471	25423471	Human	1	name
150405381	CV1177021	single nucleotide variant	NM_001083111.2(GNRH1):c.141+281A>G	not provided [RCV001544838]	likely benign	8	25422909	25422909	Human		name
150420737	CV1194037	duplication	NM_001083111.2(GNRH1):c.238-179dup	not provided [RCV001570249]	likely benign	8	25419625	25419626	Human		name
150433555	CV1204122	single nucleotide variant	NM_001083111.2(GNRH1):c.141+202A>G	not provided [RCV001581870]	likely benign	8	25422988	25422988	Human		name
152068198	CV1660220	single nucleotide variant	NM_001083111.2(GNRH1):c.63C>T (p.Cys21=)	not provided [RCV002147714]	likely benign	8	25423268	25423268	Human		name
8570006	CV29456	duplication	NM_001083111.2(GNRH1):c.18dup (p.Leu7fs)	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV000030900]	pathogenic	8	25423312	25423313	Human	1	name
597926880	CV3783376	single nucleotide variant	NM_001083111.2(GNRH1):c.60C>T (p.Gly20=)	not provided [RCV005116063]	likely benign	8	25423271	25423271	Human		name
151712474	CV1374712	duplication	NM_001083111.2(GNRH1):c.60dup (p.Cys21fs)	not provided [RCV001908290]	pathogenic	8	25423270	25423271	Human		name
9589637	CV166359	deletion	NM_001083111.2(GNRH1):c.87del (p.Leu30fs)	not provided [RCV000144705]	uncertain significance\|not provided	8	25423244	25423244	Human		name
11610544	CV313858	single nucleotide variant	NM_001083111.2(GNRH1):c.177A>G (p.Gln59=)	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV000382951]\|not provided [RCV000910936]	likely benign\|uncertain significance	8	25421633	25421633	Human	1	name
15164265	CV711467	single nucleotide variant	NM_001083111.2(GNRH1):c.183C>T (p.Phe61=)	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV001164541]\|not provided [RCV000970679]	benign	8	25421627	25421627	Human	1	name
28872734	CV899380	single nucleotide variant	NM_001083111.2(GNRH1):c.210T>A (p.Ser70=)	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV001164540]	uncertain significance	8	25421600	25421600	Human	1	name
151869329	CV1438837	single nucleotide variant	NM_001083111.2(GNRH1):c.92G>A (p.Arg31His)	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV003989137]\|not provided [RCV002035456]	pathogenic\|likely pathogenic	8	25423239	25423239	Human	1	name
156009373	CV2051321	single nucleotide variant	NM_001083111.2(GNRH1):c.73C>G (p.His25Asp)	not provided [RCV002820040]	uncertain significance	8	25423258	25423258	Human		name
405240906	CV2905055	single nucleotide variant	NM_001083111.2(GNRH1):c.91C>T (p.Arg31Cys)	Hypogonadotropic hypogonadism [RCV005416045]\|not provided [RCV003557387]	pathogenic\|uncertain significance	8	25423240	25423240	Human	3	name
405240911	CV2905056	single nucleotide variant	NM_001083111.2(GNRH1):c.52G>A (p.Val18Met)	not provided [RCV003557388]	uncertain significance	8	25423279	25423279	Human		name
405176692	CV2951989	single nucleotide variant	NM_001083111.2(GNRH1):c.86G>A (p.Gly29Glu)	not provided [RCV003675892]	uncertain significance	8	25423245	25423245	Human		name
11602158	CV313859	single nucleotide variant	NM_001083111.2(GNRH1):c.47G>C (p.Trp16Ser)	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV000288329]\|not provided [RCV000711848]	benign\|likely benign	8	25423284	25423284	Human	5	name
597788554	CV3678328	single nucleotide variant	NM_001083111.2(GNRH1):c.49T>C (p.Cys17Arg)	not specified [RCV004932772]	uncertain significance	8	25423282	25423282	Human		name
151733251	CV1336521	single nucleotide variant	NM_001083111.2(GNRH1):c.143T>G (p.Ile48Arg)	Amenorrhea [RCV001849750]\|not provided [RCV005095331]	uncertain significance	8	25421667	25421667	Human	2	name
151767557	CV1407851	single nucleotide variant	NM_001083111.2(GNRH1):c.178C>T (p.Arg60Cys)	not provided [RCV001914658]	uncertain significance	8	25421632	25421632	Human		name
151814555	CV1452853	single nucleotide variant	NM_001083111.2(GNRH1):c.270G>T (p.Lys90Asn)	not provided [RCV001900283]	conflicting interpretations of pathogenicity\|uncertain significance	8	25419428	25419428	Human		name
156022065	CV2141367	single nucleotide variant	NM_001083111.2(GNRH1):c.194C>T (p.Thr65Met)	not provided [RCV002976202]	uncertain significance	8	25421616	25421616	Human		name
598232837	CV3974431	single nucleotide variant	NM_001083111.2(GNRH1):c.143T>C (p.Ile48Thr)	not specified [RCV005342663]	uncertain significance	8	25421667	25421667	Human		name
15185969	CV700536	single nucleotide variant	NM_001083111.2(GNRH1):c.238G>C (p.Glu80Gln)	not provided [RCV000953141]	benign	8	25419460	25419460	Human		name
15192101	CV736598	single nucleotide variant	NM_001083111.2(GNRH1):c.141G>C (p.Glu47Asp)	Hypogonadotropic hypogonadism 12 with or without anosmia [RCV001164542]\|not provided [RCV000910439]	benign\|likely benign\|uncertain significance	8	25423190	25423190	Human	1	name

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