Fam170a Variant Search Result - Rat Genome Database

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44 records found for search term Fam170a

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156190988	CV2385130	single nucleotide variant	NM_001367956.1(FAM170A):c.6A>T (p.Lys2Asn)	not specified [RCV004228388]	uncertain significance	5	119629774	119629774	Human		name
597738016	CV3668673	single nucleotide variant	NM_001367956.1(FAM170A):c.13C>A (p.Gln5Lys)	not specified [RCV004920954]	uncertain significance	5	119629781	119629781	Human		name
156189627	CV2302964	single nucleotide variant	NM_001367956.1(FAM170A):c.74T>A (p.Met25Lys)	not specified [RCV004156496]	uncertain significance	5	119632751	119632751	Human		name
405743865	CV3259972	single nucleotide variant	NM_001367956.1(FAM170A):c.83C>T (p.Ser28Phe)	not specified [RCV004380927]	uncertain significance	5	119632760	119632760	Human		name
156201813	CV2300580	single nucleotide variant	NM_001367956.1(FAM170A):c.166G>A (p.Glu56Lys)	not specified [RCV004155543]	uncertain significance	5	119632843	119632843	Human		name
155992749	CV2379344	single nucleotide variant	NM_001367956.1(FAM170A):c.230G>A (p.Arg77Gln)	not specified [RCV004223804]	likely benign	5	119633978	119633978	Human		name
155955645	CV2387140	single nucleotide variant	NM_001367956.1(FAM170A):c.112A>T (p.Thr38Ser)	not specified [RCV004238249]	uncertain significance	5	119632789	119632789	Human		name
329392515	CV2439038	single nucleotide variant	NM_001367956.1(FAM170A):c.151G>A (p.Val51Ile)	not specified [RCV004264541]	uncertain significance	5	119632828	119632828	Human		name
401782309	CV2686672	single nucleotide variant	NM_001367956.1(FAM170A):c.143T>C (p.Val48Ala)	not specified [RCV004300084]	uncertain significance	5	119632820	119632820	Human		name
401738317	CV2714409	single nucleotide variant	NM_001367956.1(FAM170A):c.128G>A (p.Gly43Asp)	not specified [RCV004317942]	uncertain significance	5	119632805	119632805	Human		name
405728130	CV3259963	single nucleotide variant	NM_001367956.1(FAM170A):c.122C>T (p.Ala41Val)	not specified [RCV004378844]	uncertain significance	5	119632799	119632799	Human		name
407508221	CV3435545	single nucleotide variant	NM_001367956.1(FAM170A):c.292C>T (p.Arg98Cys)	not specified [RCV004625350]	likely benign	5	119634040	119634040	Human		name
597737985	CV3668667	single nucleotide variant	NM_001367956.1(FAM170A):c.178T>C (p.Cys60Arg)	not specified [RCV004920948]	uncertain significance	5	119632855	119632855	Human		name
597737990	CV3668668	single nucleotide variant	NM_001367956.1(FAM170A):c.119T>C (p.Val40Ala)	not specified [RCV004920949]	uncertain significance	5	119632796	119632796	Human		name
597738006	CV3668671	single nucleotide variant	NM_001367956.1(FAM170A):c.169T>C (p.Tyr57His)	not specified [RCV004920952]	uncertain significance	5	119632846	119632846	Human		name
598225313	CV3965973	single nucleotide variant	NM_001367956.1(FAM170A):c.118G>A (p.Val40Met)	not specified [RCV005341429]	uncertain significance	5	119632795	119632795	Human		name
156358474	CV2251114	single nucleotide variant	NM_001367956.1(FAM170A):c.554G>T (p.Ser185Ile)	not specified [RCV004123654]	uncertain significance	5	119634302	119634302	Human		name
156173050	CV2284009	single nucleotide variant	NM_001367956.1(FAM170A):c.889A>G (p.Lys297Glu)	not specified [RCV004144623]	likely benign	5	119634637	119634637	Human		name
155978121	CV2321357	single nucleotide variant	NM_001367956.1(FAM170A):c.706G>T (p.Val236Leu)	not specified [RCV004177358]	uncertain significance	5	119634454	119634454	Human		name
155935756	CV2383583	single nucleotide variant	NM_001367956.1(FAM170A):c.782A>G (p.His261Arg)	not specified [RCV004224451]	uncertain significance	5	119634530	119634530	Human		name
156005290	CV2393973	single nucleotide variant	NM_001367956.1(FAM170A):c.673G>A (p.Glu225Lys)	not specified [RCV004236201]	uncertain significance	5	119634421	119634421	Human		name
155933268	CV2399291	single nucleotide variant	NM_001367956.1(FAM170A):c.806G>T (p.Gly269Val)	not specified [RCV004242585]	uncertain significance	5	119634554	119634554	Human		name
329362070	CV2456710	single nucleotide variant	NM_001367956.1(FAM170A):c.974C>T (p.Pro325Leu)	not specified [RCV004277877]	uncertain significance	5	119634722	119634722	Human		name
401722975	CV2703565	single nucleotide variant	NM_001367956.1(FAM170A):c.862A>G (p.Lys288Glu)	not specified [RCV004317734]	likely benign	5	119634610	119634610	Human		name
401762031	CV2713986	single nucleotide variant	NM_001367956.1(FAM170A):c.902G>A (p.Gly301Glu)	not specified [RCV004315397]	likely benign	5	119634650	119634650	Human		name
401764276	CV2725506	single nucleotide variant	NM_001367956.1(FAM170A):c.958T>C (p.Cys320Arg)	not specified [RCV004320127]	uncertain significance	5	119634706	119634706	Human		name
405743913	CV3259965	single nucleotide variant	NM_001367956.1(FAM170A):c.311T>C (p.Leu104Ser)	not specified [RCV004380920]	uncertain significance	5	119634059	119634059	Human		name
405743906	CV3259966	single nucleotide variant	NM_001367956.1(FAM170A):c.340G>A (p.Val114Met)	not specified [RCV004380921]	uncertain significance	5	119634088	119634088	Human		name
405743899	CV3259967	single nucleotide variant	NM_001367956.1(FAM170A):c.362A>C (p.Lys121Thr)	not specified [RCV004380922]	uncertain significance	5	119634110	119634110	Human		name
405743891	CV3259968	single nucleotide variant	NM_001367956.1(FAM170A):c.439G>A (p.Glu147Lys)	not specified [RCV004380923]	uncertain significance	5	119634187	119634187	Human		name
405743886	CV3259969	single nucleotide variant	NM_001367956.1(FAM170A):c.441A>C (p.Glu147Asp)	not specified [RCV004380924]	uncertain significance	5	119634189	119634189	Human		name
405743880	CV3259970	single nucleotide variant	NM_001367956.1(FAM170A):c.704G>A (p.Arg235Gln)	not specified [RCV004380925]	uncertain significance	5	119634452	119634452	Human		name
405743873	CV3259971	single nucleotide variant	NM_001367956.1(FAM170A):c.736C>T (p.His246Tyr)	not specified [RCV004380926]	uncertain significance	5	119634484	119634484	Human		name
405743855	CV3259973	single nucleotide variant	NM_001367956.1(FAM170A):c.881C>T (p.Pro294Leu)	not specified [RCV004380928]	uncertain significance	5	119634629	119634629	Human		name
407508225	CV3435546	single nucleotide variant	NM_001367956.1(FAM170A):c.320A>G (p.Tyr107Cys)	not specified [RCV004625351]	uncertain significance	5	119634068	119634068	Human		name
597737996	CV3668669	single nucleotide variant	NM_001367956.1(FAM170A):c.713C>T (p.Thr238Ile)	not specified [RCV004920950]	uncertain significance	5	119634461	119634461	Human		name
597738001	CV3668670	single nucleotide variant	NM_001367956.1(FAM170A):c.683T>G (p.Phe228Cys)	not specified [RCV004920951]	uncertain significance	5	119634431	119634431	Human		name
597738011	CV3668672	single nucleotide variant	NM_001367956.1(FAM170A):c.979G>A (p.Asp327Asn)	not specified [RCV004920953]	uncertain significance	5	119634727	119634727	Human		name
597738021	CV3668674	single nucleotide variant	NM_001367956.1(FAM170A):c.614G>A (p.Gly205Asp)	not specified [RCV004920955]	uncertain significance	5	119634362	119634362	Human		name
597738026	CV3668675	single nucleotide variant	NM_001367956.1(FAM170A):c.367G>A (p.Glu123Lys)	not specified [RCV004920956]	uncertain significance	5	119634115	119634115	Human		name
597738031	CV3668676	single nucleotide variant	NM_001367956.1(FAM170A):c.977A>G (p.Lys326Arg)	not specified [RCV004920957]	uncertain significance	5	119634725	119634725	Human		name
598225303	CV3965971	single nucleotide variant	NM_001367956.1(FAM170A):c.679G>A (p.Gly227Ser)	not specified [RCV005341427]	uncertain significance	5	119634427	119634427	Human		name
598225308	CV3965972	single nucleotide variant	NM_001367956.1(FAM170A):c.812T>C (p.Met271Thr)	not specified [RCV005341428]	uncertain significance	5	119634560	119634560	Human		name
8625898	CV81022	single nucleotide variant	NM_001163991.1(FAM170A):c.733G>A (p.Glu245Lys)	Malignant melanoma [RCV000061100]	not provided	5	119634622	119634622	Human		name

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