Fam110c Variant Search Result - Rat Genome Database

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49 records found for search term Fam110c

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156077251	CV2251494	single nucleotide variant	NM_001077710.3(FAM110C):c.13G>A (p.Ala5Thr)	not specified [RCV004117467]	uncertain significance	2	46373	46373	Human		name
156253248	CV2325485	single nucleotide variant	NM_001077710.3(FAM110C):c.25G>A (p.Ala9Thr)	not specified [RCV004179935]	uncertain significance	2	46361	46361	Human		name
156092488	CV2302513	single nucleotide variant	NM_001077710.3(FAM110C):c.28C>T (p.Pro10Ser)	not specified [RCV004161236]	uncertain significance	2	46358	46358	Human		name
155915897	CV2339228	single nucleotide variant	NM_001077710.3(FAM110C):c.86C>T (p.Ala29Val)	not specified [RCV004191469]	uncertain significance	2	46300	46300	Human		name
156056185	CV2343452	single nucleotide variant	NM_001077710.3(FAM110C):c.89G>A (p.Arg30Gln)	not specified [RCV004197524]	uncertain significance	2	46297	46297	Human		name
405725135	CV3249686	single nucleotide variant	NM_001077710.3(FAM110C):c.53G>C (p.Arg18Pro)	not specified [RCV004378506]	uncertain significance	2	46333	46333	Human		name
405725187	CV3249691	single nucleotide variant	NM_001077710.3(FAM110C):c.98G>A (p.Arg33His)	not specified [RCV004378511]	uncertain significance	2	46288	46288	Human		name
405725200	CV3249692	single nucleotide variant	NM_001077710.3(FAM110C):c.98G>T (p.Arg33Leu)	not specified [RCV004378512]	uncertain significance	2	46288	46288	Human		name
597718950	CV3671837	single nucleotide variant	NM_001077710.3(FAM110C):c.73G>C (p.Asp25His)	not specified [RCV004918583]	uncertain significance	2	46313	46313	Human		name
156049922	CV2271841	single nucleotide variant	NM_001077710.3(FAM110C):c.259C>A (p.Arg87Ser)	not specified [RCV004130667]	uncertain significance	2	46127	46127	Human		name
156177644	CV2317263	single nucleotide variant	NM_001077710.3(FAM110C):c.130C>T (p.Arg44Cys)	not specified [RCV004178758]	uncertain significance	2	46256	46256	Human		name
155985582	CV2344533	single nucleotide variant	NM_001077710.3(FAM110C):c.187A>G (p.Ser63Gly)	not specified [RCV004195268]	uncertain significance	2	46199	46199	Human		name
401765711	CV2683397	single nucleotide variant	NM_001077710.3(FAM110C):c.245C>G (p.Pro82Arg)	not specified [RCV004288166]	uncertain significance	2	46141	46141	Human		name
401735005	CV2690743	single nucleotide variant	NM_001077710.3(FAM110C):c.211C>T (p.Pro71Ser)	not specified [RCV004298465]	uncertain significance	2	46175	46175	Human		name
401882713	CV2774805	single nucleotide variant	NM_001077710.3(FAM110C):c.226G>T (p.Gly76Trp)	not specified [RCV004343898]	uncertain significance	2	46160	46160	Human		name
405724847	CV3249677	single nucleotide variant	NM_001077710.3(FAM110C):c.145C>T (p.Arg49Trp)	not specified [RCV004378497]	uncertain significance	2	46241	46241	Human		name
405724855	CV3249678	single nucleotide variant	NM_001077710.3(FAM110C):c.151C>T (p.Arg51Trp)	not specified [RCV004378498]	uncertain significance	2	46235	46235	Human		name
405725074	CV3249680	single nucleotide variant	NM_001077710.3(FAM110C):c.220G>T (p.Asp74Tyr)	not specified [RCV004378500]	uncertain significance	2	46166	46166	Human		name
407507760	CV3435390	single nucleotide variant	NM_001077710.3(FAM110C):c.238C>T (p.Arg80Cys)	not specified [RCV004625195]	uncertain significance	2	46148	46148	Human		name
597718972	CV3671840	single nucleotide variant	NM_001077710.3(FAM110C):c.194C>T (p.Pro65Leu)	not specified [RCV004918586]	uncertain significance	2	46192	46192	Human		name
598223726	CV3965716	single nucleotide variant	NM_001077710.3(FAM110C):c.266C>T (p.Ala89Val)	not specified [RCV005341196]	uncertain significance	2	46120	46120	Human		name
598223740	CV3965718	single nucleotide variant	NM_001077710.3(FAM110C):c.236C>T (p.Ala79Val)	not specified [RCV005341198]	uncertain significance	2	46150	46150	Human		name
598194878	CV3965720	single nucleotide variant	NM_001077710.3(FAM110C):c.106G>T (p.Ala36Ser)	not specified [RCV005335479]	uncertain significance	2	46280	46280	Human		name
155641267	CV1305773	single nucleotide variant	NM_001077710.3(FAM110C):c.691G>C (p.Ala231Pro)	Streaky metaphyseal sclerosis [RCV002292653]	pathogenic	2	45695	45695	Human	1	name
155641268	CV1305774	single nucleotide variant	NM_001077710.3(FAM110C):c.690G>C (p.Glu230Asp)	Streaky metaphyseal sclerosis [RCV002292654]	pathogenic	2	45696	45696	Human	1	name
156257924	CV2219931	single nucleotide variant	NM_001077710.3(FAM110C):c.580C>T (p.Arg194Cys)	not specified [RCV004095556]	uncertain significance	2	45806	45806	Human		name
155924829	CV2248877	single nucleotide variant	NM_001077710.3(FAM110C):c.523G>A (p.Ala175Thr)	not specified [RCV004115885]	uncertain significance	2	45863	45863	Human		name
156079644	CV2258065	single nucleotide variant	NM_001077710.3(FAM110C):c.764C>A (p.Thr255Asn)	not specified [RCV004121469]	uncertain significance	2	45622	45622	Human		name
156284647	CV2317559	single nucleotide variant	NM_001077710.3(FAM110C):c.520T>C (p.Ser174Pro)	not specified [RCV004172513]	uncertain significance	2	45866	45866	Human		name
156189853	CV2356673	single nucleotide variant	NM_001077710.3(FAM110C):c.602A>C (p.Gln201Pro)	not specified [RCV004202032]	uncertain significance	2	45784	45784	Human		name
156163590	CV2368511	single nucleotide variant	NM_001077710.3(FAM110C):c.542C>T (p.Pro181Leu)	not specified [RCV004221306]	uncertain significance	2	45844	45844	Human		name
329361502	CV2437579	single nucleotide variant	NM_001077710.3(FAM110C):c.518G>A (p.Arg173Gln)	not specified [RCV004258860]	uncertain significance	2	45868	45868	Human		name
329363595	CV2442331	single nucleotide variant	NM_001077710.3(FAM110C):c.877A>G (p.Ile293Val)	not specified [RCV004264804]	uncertain significance	2	45509	45509	Human		name
401722965	CV2677153	single nucleotide variant	NM_001077710.3(FAM110C):c.485C>A (p.Pro162His)	not specified [RCV004295787]	uncertain significance	2	45901	45901	Human		name
401734561	CV2690617	single nucleotide variant	NM_001077710.3(FAM110C):c.673G>T (p.Asp225Tyr)	not specified [RCV004304705]	uncertain significance	2	45713	45713	Human		name
401777378	CV2721696	single nucleotide variant	NM_001077710.3(FAM110C):c.827T>G (p.Leu276Arg)	not specified [RCV004316179]	uncertain significance	2	45559	45559	Human		name
405725084	CV3249681	single nucleotide variant	NM_001077710.3(FAM110C):c.325T>G (p.Phe109Val)	not specified [RCV004378501]	uncertain significance	2	46061	46061	Human		name
405725094	CV3249682	single nucleotide variant	NM_001077710.3(FAM110C):c.381C>G (p.Phe127Leu)	not specified [RCV004378502]	uncertain significance	2	46005	46005	Human		name
405725116	CV3249684	single nucleotide variant	NM_001077710.3(FAM110C):c.487G>C (p.Ala163Pro)	not specified [RCV004378504]	uncertain significance	2	45899	45899	Human		name
405725125	CV3249685	single nucleotide variant	NM_001077710.3(FAM110C):c.529C>A (p.Pro177Thr)	not specified [RCV004378505]	uncertain significance	2	45857	45857	Human		name
405725149	CV3249687	single nucleotide variant	NM_001077710.3(FAM110C):c.550C>A (p.Pro184Thr)	not specified [RCV004378507]	uncertain significance	2	45836	45836	Human		name
405725158	CV3249688	single nucleotide variant	NM_001077710.3(FAM110C):c.565C>A (p.Pro189Thr)	not specified [RCV004378508]	uncertain significance	2	45821	45821	Human		name
405725175	CV3249690	single nucleotide variant	NM_001077710.3(FAM110C):c.784C>T (p.Arg262Trp)	not specified [RCV004378510]	uncertain significance	2	45602	45602	Human		name
597718943	CV3671836	single nucleotide variant	NM_001077710.3(FAM110C):c.800A>G (p.Asp267Gly)	not specified [RCV004918582]	uncertain significance	2	45586	45586	Human		name
597718958	CV3671838	single nucleotide variant	NM_001077710.3(FAM110C):c.713C>T (p.Thr238Ile)	not specified [RCV004918584]	uncertain significance	2	45673	45673	Human		name
597718965	CV3671839	single nucleotide variant	NM_001077710.3(FAM110C):c.677C>G (p.Pro226Arg)	not specified [RCV004918585]	uncertain significance	2	45709	45709	Human		name
598223719	CV3965715	single nucleotide variant	NM_001077710.3(FAM110C):c.517C>T (p.Arg173Trp)	not specified [RCV005341195]	uncertain significance	2	45869	45869	Human		name
598223732	CV3965717	single nucleotide variant	NM_001077710.3(FAM110C):c.722C>T (p.Ser241Leu)	not specified [RCV005341197]	uncertain significance	2	45664	45664	Human		name
598223747	CV3965719	single nucleotide variant	NM_001077710.3(FAM110C):c.545C>T (p.Ala182Val)	not specified [RCV005341199]	uncertain significance	2	45841	45841	Human		name

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