Pxn Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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81 records found for search term Pxn

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15185446	CV778057	single nucleotide variant	NM_001385981.1(PXN):c.494-4C>G	not provided [RCV000952986]	likely benign	12	120222754	120222754	Human		name
15147196	CV779622	single nucleotide variant	NM_001385981.1(PXN):c.2574+8G>A	not provided [RCV000967292]	benign	12	120215095	120215095	Human		name
15162166	CV730835	single nucleotide variant	NM_001385981.1(PXN):c.2575-10T>G	not provided [RCV000881707]	benign	12	120215008	120215008	Human		name
15147199	CV713381	single nucleotide variant	NM_001385981.1(PXN):c.117A>G (p.Thr39=)	not provided [RCV000967293]	benign	12	120224274	120224274	Human		name
156048828	CV2378119	single nucleotide variant	NM_001385981.1(PXN):c.67G>A (p.Val23Met)	not specified [RCV004233040]	uncertain significance	12	120224324	120224324	Human		name
597773623	CV3592480	single nucleotide variant	NM_001385981.1(PXN):c.61C>T (p.Arg21Trp)	not specified [RCV004851771]	uncertain significance	12	120224330	120224330	Human		name
598251946	CV3898207	single nucleotide variant	NM_001385981.1(PXN):c.77C>T (p.Ser26Leu)	not specified [RCV005259334]	uncertain significance	12	120224314	120224314	Human		name
15185778	CV768906	single nucleotide variant	NM_001385981.1(PXN):c.435C>T (p.Leu145=)	not provided [RCV000931157]	likely benign	12	120222921	120222921	Human		name
155963518	CV2197927	single nucleotide variant	NM_001385981.1(PXN):c.145G>A (p.Val49Ile)	not specified [RCV004077144]	uncertain significance	12	120224246	120224246	Human		name
156295100	CV2233699	single nucleotide variant	NM_001385981.1(PXN):c.190G>T (p.Asp64Tyr)	not specified [RCV004100146]	uncertain significance	12	120224201	120224201	Human		name
156132290	CV2235308	single nucleotide variant	NM_001385981.1(PXN):c.152C>A (p.Pro51Gln)	not specified [RCV004107341]	uncertain significance	12	120224239	120224239	Human		name
155975969	CV2235969	single nucleotide variant	NM_001385981.1(PXN):c.283T>A (p.Ser95Thr)	not specified [RCV004113848]	uncertain significance	12	120223791	120223791	Human		name
329355612	CV2434320	single nucleotide variant	NM_001385981.1(PXN):c.265G>A (p.Gly89Ser)	not specified [RCV004251991]	uncertain significance	12	120223809	120223809	Human		name
405667438	CV3311970	single nucleotide variant	NM_001385981.1(PXN):c.100C>G (p.Pro34Ala)	not specified [RCV004440549]	uncertain significance	12	120224291	120224291	Human		name
405667443	CV3311971	single nucleotide variant	NM_001385981.1(PXN):c.116C>T (p.Thr39Ile)	not specified [RCV004440550]	uncertain significance	12	120224275	120224275	Human		name
405667481	CV3311978	single nucleotide variant	NM_001385981.1(PXN):c.224G>A (p.Arg75Gln)	not specified [RCV004440557]	uncertain significance	12	120224167	120224167	Human		name
405667486	CV3311979	single nucleotide variant	NM_001385981.1(PXN):c.256C>T (p.Pro86Ser)	not specified [RCV004440558]	uncertain significance	12	120223818	120223818	Human		name
407499486	CV3464890	single nucleotide variant	NM_001385981.1(PXN):c.154C>T (p.Pro52Ser)	not specified [RCV004669323]	uncertain significance	12	120224237	120224237	Human		name
597773611	CV3592477	single nucleotide variant	NM_001385981.1(PXN):c.241C>T (p.Pro81Ser)	not specified [RCV004851768]	uncertain significance	12	120223833	120223833	Human		name
598251904	CV3898199	single nucleotide variant	NM_001385981.1(PXN):c.166G>A (p.Glu56Lys)	not specified [RCV005259326]	uncertain significance	12	120224225	120224225	Human		name
598251912	CV3898201	single nucleotide variant	NM_001385981.1(PXN):c.203A>G (p.Gln68Arg)	not specified [RCV005259328]	uncertain significance	12	120224188	120224188	Human		name
598251941	CV3898206	single nucleotide variant	NM_001385981.1(PXN):c.227T>A (p.Phe76Tyr)	not specified [RCV005259333]	uncertain significance	12	120224164	120224164	Human		name
15199745	CV702165	single nucleotide variant	NM_001385981.1(PXN):c.2718C>T (p.Arg906=)	not provided [RCV000957126]	benign	12	120214855	120214855	Human		name
15190659	CV724934	single nucleotide variant	NM_001385981.1(PXN):c.2991G>A (p.Thr997=)	not provided [RCV000888161]	benign	12	120212569	120212569	Human		name
156368276	CV2199809	single nucleotide variant	NM_001385981.1(PXN):c.700G>A (p.Ala234Thr)	not specified [RCV004074010]	uncertain significance	12	120221754	120221754	Human		name
156050512	CV2237792	single nucleotide variant	NM_001385981.1(PXN):c.610C>T (p.Arg204Trp)	not specified [RCV004109036]	uncertain significance	12	120222634	120222634	Human		name
155963623	CV2254589	single nucleotide variant	NM_001385981.1(PXN):c.325T>C (p.Ser109Pro)	not specified [RCV004123935]	likely benign	12	120223749	120223749	Human		name
155924299	CV2358122	single nucleotide variant	NM_001385981.1(PXN):c.386C>T (p.Pro129Leu)	not specified [RCV004211929]	uncertain significance	12	120222970	120222970	Human		name
155995928	CV2375873	single nucleotide variant	NM_001385981.1(PXN):c.623G>A (p.Arg208Gln)	not specified [RCV004217718]	uncertain significance	12	120222621	120222621	Human		name
156214043	CV2385891	single nucleotide variant	NM_001385981.1(PXN):c.515C>G (p.Pro172Arg)	not specified [RCV004226930]	uncertain significance	12	120222729	120222729	Human		name
155931676	CV2399884	single nucleotide variant	NM_001385981.1(PXN):c.769A>G (p.Ile257Val)	not specified [RCV004246828]	uncertain significance	12	120221685	120221685	Human		name
329379755	CV2443541	single nucleotide variant	NM_001385981.1(PXN):c.407C>T (p.Thr136Met)	not specified [RCV004262370]	uncertain significance	12	120222949	120222949	Human		name
401733189	CV2691229	single nucleotide variant	NM_001385981.1(PXN):c.593C>T (p.Thr198Met)	not specified [RCV004302997]	uncertain significance	12	120222651	120222651	Human		name
401770027	CV2710827	single nucleotide variant	NM_001385981.1(PXN):c.694G>A (p.Val232Ile)	not specified [RCV004308750]	uncertain significance	12	120222550	120222550	Human		name
401862875	CV2779055	single nucleotide variant	NM_001385981.1(PXN):c.511C>T (p.Pro171Ser)	not specified [RCV004348698]	uncertain significance	12	120222733	120222733	Human		name
405667491	CV3311980	single nucleotide variant	NM_001385981.1(PXN):c.367A>C (p.Lys123Gln)	not specified [RCV004440559]	uncertain significance	12	120222989	120222989	Human		name
405667495	CV3311981	single nucleotide variant	NM_001385981.1(PXN):c.499G>A (p.Ala167Thr)	not specified [RCV004440560]	uncertain significance	12	120222745	120222745	Human		name
405667500	CV3311982	single nucleotide variant	NM_001385981.1(PXN):c.604C>G (p.Pro202Ala)	not specified [RCV004440561]	uncertain significance	12	120222640	120222640	Human		name
405667506	CV3311983	single nucleotide variant	NM_001385981.1(PXN):c.647G>C (p.Ser216Thr)	not specified [RCV004440562]	uncertain significance	12	120222597	120222597	Human		name
405667511	CV3311984	single nucleotide variant	NM_001385981.1(PXN):c.802G>A (p.Glu268Lys)	not specified [RCV004440563]	uncertain significance	12	120221652	120221652	Human		name
405667516	CV3311985	single nucleotide variant	NM_001385981.1(PXN):c.815C>T (p.Ser272Leu)	not specified [RCV004440564]	uncertain significance	12	120221639	120221639	Human		name
407473758	CV3464885	single nucleotide variant	NM_001385981.1(PXN):c.503A>T (p.Asn168Ile)	not specified [RCV004662827]	uncertain significance	12	120222741	120222741	Human		name
407499482	CV3464889	single nucleotide variant	NM_001385981.1(PXN):c.320C>T (p.Pro107Leu)	not specified [RCV004669322]	uncertain significance	12	120223754	120223754	Human		name
408377569	CV3500769	single nucleotide variant	NM_001385981.1(PXN):c.379G>A (p.Ala127Thr)	not provided [RCV004722419]	likely benign	12	120222977	120222977	Human		name
597773607	CV3592476	single nucleotide variant	NM_001385981.1(PXN):c.682G>A (p.Val228Met)	not specified [RCV004851767]	uncertain significance	12	120222562	120222562	Human		name
597773619	CV3592479	single nucleotide variant	NM_001385981.1(PXN):c.718G>T (p.Gly240Cys)	not specified [RCV004851770]	uncertain significance	12	120221736	120221736	Human		name
597773653	CV3592487	single nucleotide variant	NM_001385981.1(PXN):c.346C>T (p.His116Tyr)	not specified [RCV004851778]	uncertain significance	12	120223728	120223728	Human		name
598251895	CV3898197	single nucleotide variant	NM_001385981.1(PXN):c.766C>T (p.Arg256Cys)	not specified [RCV005259324]	uncertain significance	12	120221688	120221688	Human		name
598251907	CV3898200	single nucleotide variant	NM_001385981.1(PXN):c.734C>T (p.Pro245Leu)	not specified [RCV005259327]	uncertain significance	12	120221720	120221720	Human		name
598251923	CV3898203	single nucleotide variant	NM_001385981.1(PXN):c.511C>G (p.Pro171Ala)	not specified [RCV005259330]	uncertain significance	12	120222733	120222733	Human		name
156042183	CV2261437	single nucleotide variant	NM_001385981.1(PXN):c.2864G>C (p.Arg955Pro)	not specified [RCV004130061]	uncertain significance	12	120213957	120213957	Human		name
156004905	CV2296052	single nucleotide variant	NM_001385981.1(PXN):c.2308G>C (p.Gly770Arg)	not specified [RCV004153719]	uncertain significance	12	120215655	120215655	Human		name
156208861	CV2298157	single nucleotide variant	NM_001385981.1(PXN):c.2395G>A (p.Glu799Lys)	not specified [RCV004159818]	uncertain significance	12	120215568	120215568	Human		name
156301965	CV2319448	single nucleotide variant	NM_001385981.1(PXN):c.2941C>T (p.Leu981Phe)	not specified [RCV004185029]	uncertain significance	12	120213880	120213880	Human		name
156278502	CV2330928	single nucleotide variant	NM_001385981.1(PXN):c.2734G>A (p.Gly912Ser)	not specified [RCV004185977]	uncertain significance	12	120214839	120214839	Human		name
329389800	CV2441342	single nucleotide variant	NM_001385981.1(PXN):c.2650C>T (p.Arg884Trp)	not specified [RCV004257152]	uncertain significance	12	120214923	120214923	Human		name
329362518	CV2442125	single nucleotide variant	NM_001385981.1(PXN):c.2326G>A (p.Asp776Asn)	not specified [RCV004264320]	uncertain significance	12	120215637	120215637	Human		name
401743833	CV2684790	single nucleotide variant	NM_001385981.1(PXN):c.2545G>A (p.Gly849Arg)	not specified [RCV004293866]	uncertain significance	12	120215132	120215132	Human		name
401718403	CV2708258	single nucleotide variant	NM_001385981.1(PXN):c.2480T>C (p.Met827Thr)	not specified [RCV004311603]	uncertain significance	12	120215197	120215197	Human		name
405667449	CV3311972	single nucleotide variant	NM_001385981.1(PXN):c.2678C>T (p.Pro893Leu)	not specified [RCV004440551]	uncertain significance	12	120214895	120214895	Human		name
405667454	CV3311973	single nucleotide variant	NM_001385981.1(PXN):c.2756T>C (p.Val919Ala)	not specified [RCV004440552]	uncertain significance	12	120214210	120214210	Human		name
405667459	CV3311974	single nucleotide variant	NM_001385981.1(PXN):c.2839G>A (p.Glu947Lys)	not specified [RCV004440553]	uncertain significance	12	120213982	120213982	Human		name
405667465	CV3311975	single nucleotide variant	NM_001385981.1(PXN):c.2948C>T (p.Thr983Met)	not specified [RCV004440554]	uncertain significance	12	120213873	120213873	Human		name
405667520	CV3311986	single nucleotide variant	NM_001385981.1(PXN):c.2324C>T (p.Ala775Val)	not specified [RCV004440565]	uncertain significance	12	120215639	120215639	Human		name
407473762	CV3464886	single nucleotide variant	NM_001385981.1(PXN):c.2990C>T (p.Thr997Met)	not specified [RCV004662828]	uncertain significance	12	120212570	120212570	Human		name
407473771	CV3464888	single nucleotide variant	NM_001385981.1(PXN):c.2521G>A (p.Ala841Thr)	not specified [RCV004662830]	uncertain significance	12	120215156	120215156	Human		name
407473775	CV3464891	single nucleotide variant	NM_001385981.1(PXN):c.2644G>A (p.Gly882Arg)	not specified [RCV004662831]	uncertain significance	12	120214929	120214929	Human		name
407473779	CV3464892	single nucleotide variant	NM_001385981.1(PXN):c.2882T>A (p.Met961Lys)	not specified [RCV004662832]	uncertain significance	12	120213939	120213939	Human		name
597773599	CV3592474	single nucleotide variant	NM_001385981.1(PXN):c.2461G>A (p.Gly821Arg)	not specified [RCV004851765]	uncertain significance	12	120215216	120215216	Human		name
597773627	CV3592481	single nucleotide variant	NM_001385981.1(PXN):c.2665C>T (p.Arg889Trp)	not specified [RCV004851772]	uncertain significance	12	120214908	120214908	Human		name
597773631	CV3592482	single nucleotide variant	NM_001385981.1(PXN):c.2716C>T (p.Arg906Cys)	not specified [RCV004851773]	uncertain significance	12	120214857	120214857	Human		name
597773645	CV3592485	single nucleotide variant	NM_001385981.1(PXN):c.2887G>A (p.Ala963Thr)	not specified [RCV004851776]	uncertain significance	12	120213934	120213934	Human		name
598251899	CV3898198	single nucleotide variant	NM_001385981.1(PXN):c.2368G>A (p.Gly790Arg)	not specified [RCV005259325]	likely benign	12	120215595	120215595	Human		name
598251930	CV3898204	single nucleotide variant	NM_001385981.1(PXN):c.2314G>A (p.Glu772Lys)	not specified [RCV005259331]	uncertain significance	12	120215649	120215649	Human		name
598251935	CV3898205	single nucleotide variant	NM_001385981.1(PXN):c.2866A>G (p.Lys956Glu)	not specified [RCV005259332]	uncertain significance	12	120213955	120213955	Human		name
156179684	CV2225748	single nucleotide variant	NM_001385981.1(PXN):c.3092C>T (p.Pro1031Leu)	not specified [RCV004103162]	uncertain significance	12	120212468	120212468	Human		name
329372736	CV2428624	single nucleotide variant	NM_001385981.1(PXN):c.3077C>T (p.Ser1026Phe)	not specified [RCV004255426]	uncertain significance	12	120212483	120212483	Human		name
405667475	CV3311977	single nucleotide variant	NM_001385981.1(PXN):c.3094A>G (p.Ile1032Val)	not specified [RCV004440556]	uncertain significance	12	120212466	120212466	Human		name
597773615	CV3592478	single nucleotide variant	NM_001385981.1(PXN):c.3100G>A (p.Gly1034Ser)	not specified [RCV004851769]	uncertain significance	12	120212460	120212460	Human		name
597773641	CV3592484	single nucleotide variant	NM_001385981.1(PXN):c.3071T>A (p.Leu1024Gln)	not specified [RCV004851775]	uncertain significance	12	120212489	120212489	Human		name
597773649	CV3592486	single nucleotide variant	NM_001385981.1(PXN):c.3118A>G (p.Met1040Val)	not specified [RCV004851777]	uncertain significance	12	120212442	120212442	Human		name

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