Veph1 Variant Search Result - Rat Genome Database

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61 records found for search term Veph1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8578232	CV112611	single nucleotide variant	NM_001167911.1(VEPH1):c.906+2946A>T	Lung cancer [RCV000093134]	uncertain significance	3	157410935	157410935	Human		name
8578229	CV112608	single nucleotide variant	NM_001167911.1(VEPH1):c.1994-2569G>A	Lung cancer [RCV000093131]	uncertain significance	3	157268231	157268231	Human		name
8578231	CV112610	single nucleotide variant	NM_001167911.1(VEPH1):c.907-13117G>C	Lung cancer [RCV000093133]	uncertain significance	3	157394493	157394493	Human		name
8578230	CV112609	single nucleotide variant	NM_001167911.1(VEPH1):c.1736-11718G>T	Lung cancer [RCV000093132]	uncertain significance	3	157328919	157328919	Human		name
405806772	CV3345587	single nucleotide variant	NM_001167912.2(VEPH1):c.5A>G (p.His2Arg)	not specified [RCV004480374]	uncertain significance	3	157495345	157495345	Human		name
156353466	CV2327541	single nucleotide variant	NM_001167912.2(VEPH1):c.215C>T (p.Thr72Ile)	not specified [RCV004176844]	uncertain significance	3	157470453	157470453	Human		name
156277669	CV2352085	single nucleotide variant	NM_001167912.2(VEPH1):c.287C>T (p.Pro96Leu)	not specified [RCV004191178]	uncertain significance	3	157470381	157470381	Human		name
156253599	CV2397458	single nucleotide variant	NM_001167912.2(VEPH1):c.137C>T (p.Ser46Leu)	not specified [RCV004236933]	uncertain significance	3	157495213	157495213	Human		name
329401272	CV2442274	single nucleotide variant	NM_001167912.2(VEPH1):c.125T>A (p.Ile42Asn)	not specified [RCV004264756]	uncertain significance	3	157495225	157495225	Human		name
329398520	CV2471141	single nucleotide variant	NM_001167912.2(VEPH1):c.124A>G (p.Ile42Val)	not specified [RCV004278392]	uncertain significance	3	157495226	157495226	Human		name
401751625	CV2672520	single nucleotide variant	NM_001167912.2(VEPH1):c.279C>G (p.Asn93Lys)	not specified [RCV004287559]	uncertain significance	3	157470389	157470389	Human		name
407464865	CV3493463	single nucleotide variant	NM_001167912.2(VEPH1):c.124A>T (p.Ile42Phe)	not specified [RCV004688619]	uncertain significance	3	157495226	157495226	Human		name
597803841	CV3629579	single nucleotide variant	NM_001167912.2(VEPH1):c.287C>G (p.Pro96Arg)	not specified [RCV004881973]	uncertain significance	3	157470381	157470381	Human		name
156329654	CV2213879	single nucleotide variant	NM_001167912.2(VEPH1):c.741T>A (p.Asp247Glu)	not specified [RCV004083615]	uncertain significance	3	157414046	157414046	Human		name
156080187	CV2341308	single nucleotide variant	NM_001167912.2(VEPH1):c.757A>T (p.Ile253Phe)	not specified [RCV004186717]	uncertain significance	3	157414030	157414030	Human		name
155903089	CV2353516	single nucleotide variant	NM_001167912.2(VEPH1):c.694G>A (p.Glu232Lys)	not specified [RCV004199500]	uncertain significance	3	157428324	157428324	Human		name
156159193	CV2361483	single nucleotide variant	NM_001167912.2(VEPH1):c.325G>A (p.Ala109Thr)	not specified [RCV004221122]	uncertain significance	3	157470343	157470343	Human		name
401767242	CV2681553	single nucleotide variant	NM_001167912.2(VEPH1):c.708G>T (p.Lys236Asn)	not specified [RCV004292081]	uncertain significance	3	157414079	157414079	Human		name
405806770	CV3345586	single nucleotide variant	NM_001167912.2(VEPH1):c.383T>C (p.Leu128Ser)	not specified [RCV004480373]	uncertain significance	3	157460327	157460327	Human		name
407529594	CV3493464	single nucleotide variant	NM_001167912.2(VEPH1):c.811A>G (p.Ser271Gly)	not specified [RCV004680994]	likely benign	3	157413976	157413976	Human		name
407529596	CV3493465	single nucleotide variant	NM_001167912.2(VEPH1):c.481G>A (p.Asp161Asn)	not specified [RCV004680995]	uncertain significance	3	157460229	157460229	Human		name
408368186	CV3518113	single nucleotide variant	NM_001167912.2(VEPH1):c.418G>C (p.Gly140Arg)	Congenital long QT syndrome [RCV004733995]\|not specified [RCV004877859]	uncertain significance	3	157460292	157460292	Human	1	name
597803828	CV3629571	single nucleotide variant	NM_001167912.2(VEPH1):c.779A>G (p.Glu260Gly)	not specified [RCV004881966]	uncertain significance	3	157414008	157414008	Human		name
597803830	CV3629573	single nucleotide variant	NM_001167912.2(VEPH1):c.802G>A (p.Ala268Thr)	not specified [RCV004881967]	uncertain significance	3	157413985	157413985	Human		name
597803832	CV3629574	single nucleotide variant	NM_001167912.2(VEPH1):c.515A>G (p.Lys172Arg)	not specified [RCV004881968]	uncertain significance	3	157460195	157460195	Human		name
597803838	CV3629577	single nucleotide variant	NM_001167912.2(VEPH1):c.310C>G (p.Pro104Ala)	not specified [RCV004881971]	uncertain significance	3	157470358	157470358	Human		name
597803840	CV3629578	single nucleotide variant	NM_001167912.2(VEPH1):c.823A>G (p.Met275Val)	not specified [RCV004881972]	uncertain significance	3	157413964	157413964	Human		name
597698480	CV3629581	single nucleotide variant	NM_001167912.2(VEPH1):c.538A>T (p.Met180Leu)	not specified [RCV004885381]	uncertain significance	3	157428480	157428480	Human		name
598240483	CV3929545	single nucleotide variant	NM_001167912.2(VEPH1):c.310C>T (p.Pro104Ser)	not specified [RCV005296776]	uncertain significance	3	157470358	157470358	Human		name
598240489	CV3929546	single nucleotide variant	NM_001167912.2(VEPH1):c.718T>C (p.Phe240Leu)	not specified [RCV005296777]	uncertain significance	3	157414069	157414069	Human		name
598240497	CV3929549	single nucleotide variant	NM_001167912.2(VEPH1):c.304G>A (p.Asp102Asn)	not specified [RCV005296778]	uncertain significance	3	157470364	157470364	Human		name
598205875	CV3929551	single nucleotide variant	NM_001167912.2(VEPH1):c.647A>G (p.Tyr216Cys)	not specified [RCV005290922]	uncertain significance	3	157428371	157428371	Human		name
156397664	CV2197397	single nucleotide variant	NM_001167912.2(VEPH1):c.1861T>C (p.Phe621Leu)	not specified [RCV004081136]	uncertain significance	3	157317076	157317076	Human		name
156063598	CV2240166	single nucleotide variant	NM_001167912.2(VEPH1):c.1621A>G (p.Ile541Val)	not specified [RCV004110924]	likely benign	3	157363478	157363478	Human		name
156048658	CV2241700	single nucleotide variant	NM_001167912.2(VEPH1):c.2109C>A (p.Asn703Lys)	not specified [RCV004106645]	uncertain significance	3	157286576	157286576	Human		name
155963563	CV2254578	single nucleotide variant	NM_001167912.2(VEPH1):c.2199C>G (p.Ile733Met)	not specified [RCV004123926]	uncertain significance	3	157265592	157265592	Human		name
156048912	CV2271758	single nucleotide variant	NM_001167912.2(VEPH1):c.1060A>G (p.Asn354Asp)	not specified [RCV004130602]	uncertain significance	3	157381223	157381223	Human		name
156305269	CV2338725	single nucleotide variant	NM_001167912.2(VEPH1):c.1378G>A (p.Val460Met)	not specified [RCV004599565]	uncertain significance	3	157363721	157363721	Human		name
155927500	CV2349620	single nucleotide variant	NM_001167912.2(VEPH1):c.1393G>A (p.Gly465Ser)	not specified [RCV004204041]	uncertain significance	3	157363706	157363706	Human		name
156178787	CV2355960	single nucleotide variant	NM_001167912.2(VEPH1):c.1047C>G (p.Ile349Met)	not specified [RCV004201341]	uncertain significance	3	157381236	157381236	Human		name
156134167	CV2361970	single nucleotide variant	NM_001167912.2(VEPH1):c.2059G>A (p.Val687Met)	not specified [RCV004207737]	uncertain significance	3	157286626	157286626	Human		name
156387254	CV2372690	single nucleotide variant	NM_001167912.2(VEPH1):c.1805G>A (p.Ser602Asn)	not specified [RCV004221886]	uncertain significance	3	157317132	157317132	Human		name
329374098	CV2463309	single nucleotide variant	NM_001167912.2(VEPH1):c.2216G>A (p.Arg739His)	not specified [RCV004275369]	uncertain significance	3	157265575	157265575	Human		name
401756914	CV2678124	single nucleotide variant	NM_001167912.2(VEPH1):c.2185A>G (p.Arg729Gly)	not specified [RCV004296637]	uncertain significance	3	157265606	157265606	Human		name
401735783	CV2695399	single nucleotide variant	NM_001167912.2(VEPH1):c.1267C>G (p.Pro423Ala)	not specified [RCV004305603]	uncertain significance	3	157364373	157364373	Human		name
401876889	CV2793271	single nucleotide variant	NM_001167912.2(VEPH1):c.2260A>C (p.Lys754Gln)	not specified [RCV004362094]	uncertain significance	3	157265531	157265531	Human		name
405806757	CV3345580	single nucleotide variant	NM_001167912.2(VEPH1):c.1184T>C (p.Ile395Thr)	not specified [RCV004480367]	likely benign	3	157364456	157364456	Human		name
405806760	CV3345581	single nucleotide variant	NM_001167912.2(VEPH1):c.1217A>T (p.Gln406Leu)	not specified [RCV004480368]	uncertain significance	3	157364423	157364423	Human		name
405806762	CV3345582	single nucleotide variant	NM_001167912.2(VEPH1):c.1477C>T (p.Pro493Ser)	not specified [RCV004480369]	uncertain significance	3	157363622	157363622	Human		name
405806923	CV3345583	single nucleotide variant	NM_001167912.2(VEPH1):c.1610C>T (p.Thr537Ile)	not specified [RCV004480370]	uncertain significance	3	157363489	157363489	Human		name
405806766	CV3345584	single nucleotide variant	NM_001167912.2(VEPH1):c.1685C>T (p.Ala562Val)	not specified [RCV004480371]	uncertain significance	3	157363414	157363414	Human		name
405806768	CV3345585	single nucleotide variant	NM_001167912.2(VEPH1):c.2149C>T (p.Pro717Ser)	not specified [RCV004480372]	uncertain significance	3	157265642	157265642	Human		name
407529590	CV3493461	single nucleotide variant	NM_001167912.2(VEPH1):c.2215C>T (p.Arg739Cys)	not specified [RCV004680992]	uncertain significance	3	157265576	157265576	Human		name
407529592	CV3493462	single nucleotide variant	NM_001167912.2(VEPH1):c.1726A>G (p.Thr576Ala)	not specified [RCV004680993]	uncertain significance	3	157363373	157363373	Human		name
597698474	CV3629572	single nucleotide variant	NM_001167912.2(VEPH1):c.1091C>A (p.Thr364Asn)	not specified [RCV004885380]	uncertain significance	3	157381192	157381192	Human		name
597803834	CV3629575	single nucleotide variant	NM_001167912.2(VEPH1):c.1421C>A (p.Pro474Gln)	not specified [RCV004881969]	uncertain significance	3	157363678	157363678	Human		name
597803836	CV3629576	single nucleotide variant	NM_001167912.2(VEPH1):c.1635T>A (p.Asp545Glu)	not specified [RCV004881970]	uncertain significance	3	157363464	157363464	Human		name
598205855	CV3929544	single nucleotide variant	NM_001167912.2(VEPH1):c.2084G>A (p.Gly695Glu)	not specified [RCV005290919]	uncertain significance	3	157286601	157286601	Human		name
598205862	CV3929547	single nucleotide variant	NM_001167912.2(VEPH1):c.1256G>A (p.Gly419Glu)	not specified [RCV005290920]	likely benign	3	157364384	157364384	Human		name
598205869	CV3929548	single nucleotide variant	NM_001167912.2(VEPH1):c.1396G>A (p.Glu466Lys)	not specified [RCV005290921]	uncertain significance	3	157363703	157363703	Human		name
598240505	CV3929550	single nucleotide variant	NM_001167912.2(VEPH1):c.1933C>A (p.Leu645Met)	not specified [RCV005296779]	uncertain significance	3	157313698	157313698	Human		name

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