Serpina5 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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57 records found for search term Serpina5

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156070584	CV2381326	single nucleotide variant	NM_000624.6(SERPINA5):c.62G>A (p.Arg21His)	not specified [RCV004227385]	uncertain significance	14	94587424	94587424	Human		name
405747308	CV3310945	single nucleotide variant	NM_000624.6(SERPINA5):c.73C>T (p.Arg25Trp)	not specified [RCV004453245]	uncertain significance	14	94587435	94587435	Human		name
597738090	CV3598522	single nucleotide variant	NM_000624.6(SERPINA5):c.73C>G (p.Arg25Gly)	not specified [RCV004864178]	uncertain significance	14	94587435	94587435	Human		name
598225700	CV3900429	single nucleotide variant	NM_000624.6(SERPINA5):c.44A>C (p.Gln15Pro)	not specified [RCV005273396]	uncertain significance	14	94587406	94587406	Human		name
155919262	CV2254836	single nucleotide variant	NM_000624.6(SERPINA5):c.158A>T (p.Tyr53Phe)	not specified [RCV004115297]	uncertain significance	14	94587520	94587520	Human		name
156088573	CV2337193	single nucleotide variant	NM_000624.6(SERPINA5):c.265A>T (p.Met89Leu)	not specified [RCV004192949]	uncertain significance	14	94587627	94587627	Human		name
401730714	CV2677269	single nucleotide variant	NM_000624.6(SERPINA5):c.109G>A (p.Gly37Ser)	not specified [RCV004295889]	uncertain significance	14	94587471	94587471	Human		name
401761814	CV2726918	single nucleotide variant	NM_000624.6(SERPINA5):c.294C>A (p.Asn98Lys)	not specified [RCV004323203]	uncertain significance	14	94587656	94587656	Human		name
401898424	CV2787892	single nucleotide variant	NM_000624.6(SERPINA5):c.155T>C (p.Leu52Pro)	not specified [RCV004358569]	uncertain significance	14	94587517	94587517	Human		name
405747274	CV3310940	single nucleotide variant	NM_000624.6(SERPINA5):c.185G>A (p.Ser62Asn)	not specified [RCV004453240]	uncertain significance	14	94587547	94587547	Human		name
598225694	CV3900428	single nucleotide variant	NM_000624.6(SERPINA5):c.224G>A (p.Ser75Asn)	not specified [RCV005273395]	uncertain significance	14	94587586	94587586	Human		name
598225713	CV3900431	single nucleotide variant	NM_000624.6(SERPINA5):c.163G>A (p.Ala55Thr)	not specified [RCV005273398]	uncertain significance	14	94587525	94587525	Human		name
15122731	CV739403	single nucleotide variant	NM_000624.6(SERPINA5):c.1002C>T (p.Ser334=)	not provided [RCV000896289]	benign	14	94590860	94590860	Human		name
156238771	CV2268992	single nucleotide variant	NM_000624.6(SERPINA5):c.482A>T (p.Asn161Ile)	not specified [RCV004128390]	uncertain significance	14	94587844	94587844	Human		name
156133801	CV2361919	single nucleotide variant	NM_000624.6(SERPINA5):c.742C>G (p.Arg248Gly)	not specified [RCV004207691]	uncertain significance	14	94590163	94590163	Human		name
156341665	CV2368440	single nucleotide variant	NM_000624.6(SERPINA5):c.343C>A (p.Leu115Ile)	not specified [RCV004219203]	uncertain significance	14	94587705	94587705	Human		name
329377524	CV2435947	single nucleotide variant	NM_000624.6(SERPINA5):c.932C>T (p.Ser311Phe)	not specified [RCV004255170]	uncertain significance	14	94590790	94590790	Human		name
329383012	CV2441758	single nucleotide variant	NM_000624.6(SERPINA5):c.747C>A (p.Asn249Lys)	not specified [RCV004261971]	uncertain significance	14	94590168	94590168	Human		name
329390608	CV2459341	single nucleotide variant	NM_000624.6(SERPINA5):c.331T>A (p.Phe111Ile)	not specified [RCV004274753]	uncertain significance	14	94587693	94587693	Human		name
329375031	CV2470963	single nucleotide variant	NM_000624.6(SERPINA5):c.686C>T (p.Thr229Ile)	not specified [RCV004276149]	uncertain significance	14	94590107	94590107	Human		name
401779899	CV2676726	single nucleotide variant	NM_000624.6(SERPINA5):c.949G>A (p.Val317Ile)	not specified [RCV004290901]	likely benign	14	94590807	94590807	Human		name
401734059	CV2688391	single nucleotide variant	NM_000624.6(SERPINA5):c.652A>T (p.Thr218Ser)	not specified [RCV004299381]	uncertain significance	14	94590073	94590073	Human		name
401744070	CV2696929	single nucleotide variant	NM_000624.6(SERPINA5):c.955C>T (p.Pro319Ser)	not specified [RCV004292929]	uncertain significance	14	94590813	94590813	Human		name
401752632	CV2707074	single nucleotide variant	NM_000624.6(SERPINA5):c.406G>A (p.Asp136Asn)	not specified [RCV004321658]	uncertain significance	14	94587768	94587768	Human		name
401738757	CV2721968	single nucleotide variant	NM_000624.6(SERPINA5):c.692T>C (p.Val231Ala)	not specified [RCV004326463]	uncertain significance	14	94590113	94590113	Human		name
401877089	CV2769332	single nucleotide variant	NM_000624.6(SERPINA5):c.622A>G (p.Lys208Glu)	not specified [RCV004357328]	uncertain significance	14	94590043	94590043	Human		name
401902229	CV2807197	single nucleotide variant	NM_000624.6(SERPINA5):c.682G>C (p.Glu228Gln)	not provided [RCV003393578]	likely benign	14	94590103	94590103	Human		name
405747287	CV3310942	single nucleotide variant	NM_000624.6(SERPINA5):c.401T>A (p.Phe134Tyr)	not specified [RCV004453242]	uncertain significance	14	94587763	94587763	Human		name
405747294	CV3310943	single nucleotide variant	NM_000624.6(SERPINA5):c.439A>G (p.Ser147Gly)	not specified [RCV004453243]	uncertain significance	14	94587801	94587801	Human		name
405747300	CV3310944	single nucleotide variant	NM_000624.6(SERPINA5):c.635G>A (p.Ser212Asn)	not specified [RCV004453244]	uncertain significance	14	94590056	94590056	Human		name
405747315	CV3310946	single nucleotide variant	NM_000624.6(SERPINA5):c.892C>A (p.Gln298Lys)	not specified [RCV004453246]	uncertain significance	14	94590750	94590750	Human		name
407488886	CV3473637	single nucleotide variant	NM_000624.6(SERPINA5):c.589G>A (p.Val197Met)	not specified [RCV004665949]	likely benign	14	94587951	94587951	Human		name
407488895	CV3473639	single nucleotide variant	NM_000624.6(SERPINA5):c.566A>G (p.Lys189Arg)	not specified [RCV004665951]	uncertain significance	14	94587928	94587928	Human		name
407492467	CV3473640	single nucleotide variant	NM_000624.6(SERPINA5):c.451A>G (p.Thr151Ala)	not specified [RCV004667134]	uncertain significance	14	94587813	94587813	Human		name
407488900	CV3473641	single nucleotide variant	NM_000624.6(SERPINA5):c.958A>G (p.Ser320Gly)	not specified [RCV004665952]	uncertain significance	14	94590816	94590816	Human		name
597738080	CV3598520	single nucleotide variant	NM_000624.6(SERPINA5):c.557A>T (p.Asp186Val)	not specified [RCV004864176]	uncertain significance	14	94587919	94587919	Human		name
597738085	CV3598521	single nucleotide variant	NM_000624.6(SERPINA5):c.680C>T (p.Ser227Leu)	not specified [RCV004864177]	uncertain significance	14	94590101	94590101	Human		name
597738099	CV3598525	single nucleotide variant	NM_000624.6(SERPINA5):c.535C>G (p.Gln179Glu)	not specified [RCV004864180]	uncertain significance	14	94587897	94587897	Human		name
597738107	CV3598527	single nucleotide variant	NM_000624.6(SERPINA5):c.723G>C (p.Gln241His)	not specified [RCV004864182]	uncertain significance	14	94590144	94590144	Human		name
597738112	CV3598528	single nucleotide variant	NM_000624.6(SERPINA5):c.407A>G (p.Asp136Gly)	not specified [RCV004864183]	uncertain significance	14	94587769	94587769	Human		name
598225672	CV3900424	single nucleotide variant	NM_000624.6(SERPINA5):c.923T>C (p.Ile308Thr)	not specified [RCV005273391]	uncertain significance	14	94590781	94590781	Human		name
598225679	CV3900425	single nucleotide variant	NM_000624.6(SERPINA5):c.830A>G (p.Gln277Arg)	not specified [RCV005273392]	uncertain significance	14	94590251	94590251	Human		name
598225706	CV3900430	single nucleotide variant	NM_000624.6(SERPINA5):c.586G>T (p.Val196Phe)	not specified [RCV005273397]	uncertain significance	14	94587948	94587948	Human		name
15200117	CV703030	single nucleotide variant	NM_000624.6(SERPINA5):c.649G>C (p.Gly217Arg)	not provided [RCV000957238]	benign	14	94590070	94590070	Human		name
156110136	CV2211418	single nucleotide variant	NM_000624.6(SERPINA5):c.1003G>A (p.Gly335Ser)	not specified [RCV004090326]	uncertain significance	14	94590861	94590861	Human		name
156149117	CV2265328	single nucleotide variant	NM_000624.6(SERPINA5):c.1174A>G (p.Ile392Val)	not specified [RCV004128219]	uncertain significance	14	94592192	94592192	Human		name
156361146	CV2326391	single nucleotide variant	NM_000624.6(SERPINA5):c.1155C>A (p.Asn385Lys)	not specified [RCV004182966]	uncertain significance	14	94592173	94592173	Human		name
156018493	CV2370289	single nucleotide variant	NM_000624.6(SERPINA5):c.1213C>T (p.Arg405Cys)	not specified [RCV004213204]	uncertain significance	14	94592231	94592231	Human		name
401724542	CV2714881	single nucleotide variant	NM_000624.6(SERPINA5):c.1075G>A (p.Gly359Arg)	not specified [RCV004322219]	uncertain significance	14	94592093	94592093	Human		name
405747261	CV3310938	single nucleotide variant	NM_000624.6(SERPINA5):c.1192C>T (p.Leu398Phe)	not specified [RCV004453238]	uncertain significance	14	94592210	94592210	Human		name
405747267	CV3310939	single nucleotide variant	NM_000624.6(SERPINA5):c.1204A>G (p.Lys402Glu)	not specified [RCV004453239]	uncertain significance	14	94592222	94592222	Human		name
407488890	CV3473638	single nucleotide variant	NM_000624.6(SERPINA5):c.1120T>A (p.Ser374Thr)	not specified [RCV004665950]	uncertain significance	14	94592138	94592138	Human		name
597738095	CV3598524	single nucleotide variant	NM_000624.6(SERPINA5):c.1127G>A (p.Arg376His)	not specified [RCV004864179]	uncertain significance	14	94592145	94592145	Human		name
597738102	CV3598526	single nucleotide variant	NM_000624.6(SERPINA5):c.1196T>C (p.Phe399Ser)	not specified [RCV004864181]	uncertain significance	14	94592214	94592214	Human		name
597738115	CV3598529	single nucleotide variant	NM_000624.6(SERPINA5):c.1162T>C (p.Phe388Leu)	not specified [RCV004864184]	uncertain significance	14	94592180	94592180	Human		name
598225683	CV3900426	single nucleotide variant	NM_000624.6(SERPINA5):c.1073C>T (p.Ser358Leu)	not specified [RCV005273393]	uncertain significance	14	94592091	94592091	Human		name
8635357	CV90579	single nucleotide variant	NM_000624.5(SERPINA5):c.1099G>A (p.Gly367Arg)	Malignant melanoma [RCV000070677]	not provided	14	94592117	94592117	Human		name

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