Hic1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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67 records found for search term Hic1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405777805	CV3270179	single nucleotide variant	NM_006497.4(HIC1):c.-2C>A	not specified [RCV004397096]	uncertain significance	17	2056689	2056689	Human		name
156378248	CV2207669	single nucleotide variant	NM_006497.4(HIC1):c.-20-357C>T	not specified [RCV004084125]	uncertain significance	17	2056314	2056314	Human		name
156172687	CV2337618	single nucleotide variant	NM_006497.4(HIC1):c.-20-327C>G	not specified [RCV004181181]	uncertain significance	17	2056344	2056344	Human		name
401903678	CV2814693	single nucleotide variant	NM_006497.4(HIC1):c.7G>A (p.Asp3Asn)	not provided [RCV003419565]	uncertain significance	17	2056697	2056697	Human		name
15201505	CV727058	single nucleotide variant	NM_006497.4(HIC1):c.252C>T (p.Thr84=)	not provided [RCV000891211]	benign	17	2056942	2056942	Human		name
155961241	CV2390847	single nucleotide variant	NM_006497.4(HIC1):c.208G>A (p.Val70Met)	not specified [RCV004241120]	uncertain significance	17	2056898	2056898	Human		name
329359450	CV2451023	single nucleotide variant	NM_006497.4(HIC1):c.256C>T (p.Arg86Cys)	not specified [RCV004269688]	uncertain significance	17	2056946	2056946	Human		name
401780580	CV2674089	single nucleotide variant	NM_006497.4(HIC1):c.110C>T (p.Ala37Val)	not specified [RCV004295495]	uncertain significance	17	2056800	2056800	Human		name
597761939	CV3685843	single nucleotide variant	NM_006497.4(HIC1):c.109G>T (p.Ala37Ser)	not specified [RCV004926019]	uncertain significance	17	2056799	2056799	Human		name
15139743	CV715294	single nucleotide variant	NM_006497.4(HIC1):c.1551A>G (p.Pro517=)	not provided [RCV000966018]	benign	17	2058241	2058241	Human		name
15174766	CV727059	single nucleotide variant	NM_006497.4(HIC1):c.1143C>T (p.Ser381=)	not provided [RCV000884202]	benign	17	2057833	2057833	Human		name
15179540	CV727060	single nucleotide variant	NM_006497.4(HIC1):c.1230C>T (p.Pro410=)	not provided [RCV000885313]	benign	17	2057920	2057920	Human		name
15106309	CV727061	single nucleotide variant	NM_006497.4(HIC1):c.1416C>T (p.Asp472=)	not provided [RCV000893255]	benign	17	2058106	2058106	Human		name
15129209	CV740651	single nucleotide variant	NM_006497.4(HIC1):c.1398T>C (p.Pro466=)	not provided [RCV000897402]	likely benign	17	2058088	2058088	Human		name
15145417	CV740652	single nucleotide variant	NM_006497.4(HIC1):c.1728G>A (p.Val576=)	not provided [RCV000900158]	likely benign	17	2058418	2058418	Human		name
155986066	CV2233953	single nucleotide variant	NM_006497.4(HIC1):c.866G>A (p.Arg289His)	not specified [RCV004104296]	uncertain significance	17	2057556	2057556	Human		name
156266804	CV2305593	single nucleotide variant	NM_006497.4(HIC1):c.545C>G (p.Ala182Gly)	not specified [RCV004165610]	uncertain significance	17	2057235	2057235	Human		name
155970989	CV2309246	single nucleotide variant	NM_006497.4(HIC1):c.616C>T (p.Pro206Ser)	not specified [RCV004165415]	uncertain significance	17	2057306	2057306	Human		name
155917141	CV2336277	single nucleotide variant	NM_006497.4(HIC1):c.796G>A (p.Ala266Thr)	not specified [RCV004192029]	uncertain significance	17	2057486	2057486	Human		name
155917147	CV2336278	single nucleotide variant	NM_006497.4(HIC1):c.797C>G (p.Ala266Gly)	not specified [RCV004192030]	uncertain significance	17	2057487	2057487	Human		name
156225233	CV2390514	single nucleotide variant	NM_006497.4(HIC1):c.512C>G (p.Pro171Arg)	not specified [RCV004239050]	uncertain significance	17	2057202	2057202	Human		name
329358253	CV2425169	single nucleotide variant	NM_006497.4(HIC1):c.307G>C (p.Ala103Pro)	not specified [RCV004249056]	uncertain significance	17	2056997	2056997	Human		name
401720532	CV2701947	single nucleotide variant	NM_006497.4(HIC1):c.421G>A (p.Gly141Ser)	not specified [RCV004320550]	uncertain significance	17	2057111	2057111	Human		name
405777811	CV3270180	single nucleotide variant	NM_006497.4(HIC1):c.751A>G (p.Ser251Gly)	not specified [RCV004397097]	uncertain significance	17	2057441	2057441	Human		name
405777817	CV3270181	single nucleotide variant	NM_006497.4(HIC1):c.799C>G (p.Leu267Val)	not specified [RCV004397098]	uncertain significance	17	2057489	2057489	Human		name
405777823	CV3270182	single nucleotide variant	NM_006497.4(HIC1):c.805T>C (p.Ser269Pro)	not specified [RCV004397099]	likely benign	17	2057495	2057495	Human		name
405777829	CV3270183	single nucleotide variant	NM_006497.4(HIC1):c.866G>T (p.Arg289Leu)	not specified [RCV004397100]	uncertain significance	17	2057556	2057556	Human		name
407522161	CV3437297	single nucleotide variant	NM_006497.4(HIC1):c.691C>T (p.Pro231Ser)	not specified [RCV004630604]	uncertain significance	17	2057381	2057381	Human		name
407522164	CV3437298	single nucleotide variant	NM_006497.4(HIC1):c.929A>G (p.Tyr310Cys)	not specified [RCV004630605]	uncertain significance	17	2057619	2057619	Human		name
407522167	CV3437299	single nucleotide variant	NM_006497.4(HIC1):c.313C>T (p.Pro105Ser)	not specified [RCV004630606]	uncertain significance	17	2057003	2057003	Human		name
407522170	CV3437300	single nucleotide variant	NM_006497.4(HIC1):c.469C>T (p.Arg157Trp)	not specified [RCV004630607]	uncertain significance	17	2057159	2057159	Human		name
407522173	CV3437301	single nucleotide variant	NM_006497.4(HIC1):c.503C>A (p.Ala168Asp)	not specified [RCV004630608]	uncertain significance	17	2057193	2057193	Human		name
407522176	CV3437302	single nucleotide variant	NM_006497.4(HIC1):c.932G>A (p.Arg311His)	not specified [RCV004630609]	uncertain significance	17	2057622	2057622	Human		name
407522179	CV3437303	single nucleotide variant	NM_006497.4(HIC1):c.913G>A (p.Gly305Arg)	not specified [RCV004630610]	uncertain significance	17	2057603	2057603	Human		name
597761944	CV3685844	single nucleotide variant	NM_006497.4(HIC1):c.464C>T (p.Pro155Leu)	not specified [RCV004926020]	uncertain significance	17	2057154	2057154	Human		name
598247984	CV3978794	single nucleotide variant	NM_006497.4(HIC1):c.742C>A (p.Arg248Ser)	not specified [RCV005345380]	uncertain significance	17	2057432	2057432	Human		name
598248007	CV3978799	single nucleotide variant	NM_006497.4(HIC1):c.899C>A (p.Pro300His)	not specified [RCV005345383]	uncertain significance	17	2057589	2057589	Human		name
598177710	CV3978800	single nucleotide variant	NM_006497.4(HIC1):c.575T>G (p.Val192Gly)	not specified [RCV005351879]	uncertain significance	17	2057265	2057265	Human		name
155922516	CV2207510	single nucleotide variant	NM_006497.4(HIC1):c.1445G>A (p.Gly482Glu)	not specified [RCV004089980]	uncertain significance	17	2058135	2058135	Human		name
155946412	CV2238119	single nucleotide variant	NM_006497.4(HIC1):c.1732G>C (p.Gly578Arg)	not specified [RCV004111133]	uncertain significance	17	2058422	2058422	Human		name
156053927	CV2243023	single nucleotide variant	NM_006497.4(HIC1):c.2090C>T (p.Ala697Val)	not specified [RCV004109943]	uncertain significance	17	2058780	2058780	Human		name
156091011	CV2256550	single nucleotide variant	NM_006497.4(HIC1):c.2094C>G (p.His698Gln)	not specified [RCV004118749]	uncertain significance	17	2058784	2058784	Human		name
155997848	CV2287080	single nucleotide variant	NM_006497.4(HIC1):c.2077C>A (p.Leu693Met)	not specified [RCV004144955]	uncertain significance	17	2058767	2058767	Human		name
156152012	CV2307600	single nucleotide variant	NM_006497.4(HIC1):c.1328A>T (p.Glu443Val)	not specified [RCV004168024]	uncertain significance	17	2058018	2058018	Human		name
155916301	CV2336124	single nucleotide variant	NM_006497.4(HIC1):c.1409G>A (p.Gly470Asp)	not specified [RCV004189718]	uncertain significance	17	2058099	2058099	Human		name
156110407	CV2353258	single nucleotide variant	NM_006497.4(HIC1):c.1388T>G (p.Leu463Arg)	not specified [RCV004205737]	uncertain significance	17	2058078	2058078	Human		name
155984798	CV2368004	single nucleotide variant	NM_006497.4(HIC1):c.1270G>A (p.Gly424Ser)	not specified [RCV004223091]	uncertain significance	17	2057960	2057960	Human		name
156270487	CV2398684	single nucleotide variant	NM_006497.4(HIC1):c.1832G>A (p.Gly611Glu)	not specified [RCV004240031]	uncertain significance	17	2058522	2058522	Human		name
329392257	CV2441360	single nucleotide variant	NM_006497.4(HIC1):c.2073G>C (p.Glu691Asp)	not specified [RCV004257167]	uncertain significance	17	2058763	2058763	Human		name
401722524	CV2677016	single nucleotide variant	NM_006497.4(HIC1):c.1003G>C (p.Glu335Gln)	not specified [RCV004293617]	uncertain significance	17	2057693	2057693	Human		name
401737513	CV2699836	single nucleotide variant	NM_006497.4(HIC1):c.1694T>C (p.Ile565Thr)	not specified [RCV004308481]	uncertain significance	17	2058384	2058384	Human		name
401770697	CV2707356	single nucleotide variant	NM_006497.4(HIC1):c.2141C>G (p.Thr714Ser)	not specified [RCV004312752]	uncertain significance	17	2058831	2058831	Human		name
401733706	CV2713186	single nucleotide variant	NM_006497.4(HIC1):c.1937A>G (p.Gln646Arg)	not specified [RCV004316727]	uncertain significance	17	2058627	2058627	Human		name
401877533	CV2790203	single nucleotide variant	NM_006497.4(HIC1):c.2140A>G (p.Thr714Ala)	not specified [RCV004364122]	uncertain significance	17	2058830	2058830	Human		name
405777775	CV3270174	single nucleotide variant	NM_006497.4(HIC1):c.1006C>T (p.Arg336Cys)	not specified [RCV004397091]	uncertain significance	17	2057696	2057696	Human		name
405778423	CV3270175	single nucleotide variant	NM_006497.4(HIC1):c.1808C>T (p.Ala603Val)	not specified [RCV004397092]	uncertain significance	17	2058498	2058498	Human		name
405777799	CV3270178	single nucleotide variant	NM_006497.4(HIC1):c.2061C>A (p.Asp687Glu)	not specified [RCV004397095]	uncertain significance	17	2058751	2058751	Human		name
597761948	CV3685845	single nucleotide variant	NM_006497.4(HIC1):c.1201C>T (p.Pro401Ser)	not specified [RCV004926021]	uncertain significance	17	2057891	2057891	Human		name
597761950	CV3685846	single nucleotide variant	NM_006497.4(HIC1):c.1448A>G (p.Glu483Gly)	not specified [RCV004926022]	uncertain significance	17	2058138	2058138	Human		name
597761956	CV3685847	single nucleotide variant	NM_006497.4(HIC1):c.1173C>G (p.Ser391Arg)	not specified [RCV004926023]	uncertain significance	17	2057863	2057863	Human		name
598177691	CV3978793	single nucleotide variant	NM_006497.4(HIC1):c.1078C>G (p.Arg360Gly)	not specified [RCV005351876]	uncertain significance	17	2057768	2057768	Human		name
598247993	CV3978795	single nucleotide variant	NM_006497.4(HIC1):c.1988A>G (p.His663Arg)	not specified [RCV005345381]	uncertain significance	17	2058678	2058678	Human		name
598177697	CV3978796	single nucleotide variant	NM_006497.4(HIC1):c.1927C>G (p.Leu643Val)	not specified [RCV005351877]	uncertain significance	17	2058617	2058617	Human		name
598177703	CV3978797	single nucleotide variant	NM_006497.4(HIC1):c.1187A>C (p.His396Pro)	not specified [RCV005351878]	uncertain significance	17	2057877	2057877	Human		name
598248000	CV3978798	single nucleotide variant	NM_006497.4(HIC1):c.1499C>G (p.Pro500Arg)	not specified [RCV005345382]	uncertain significance	17	2058189	2058189	Human		name
598177717	CV3978801	single nucleotide variant	NM_006497.4(HIC1):c.1867A>G (p.Lys623Glu)	not specified [RCV005351880]	uncertain significance	17	2058557	2058557	Human		name
15161063	CV715293	single nucleotide variant	NM_006497.4(HIC1):c.1369G>A (p.Ala457Thr)	not provided [RCV000970021]	likely benign	17	2058059	2058059	Human		name

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