Plb1 Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

201 records found for search term Plb1

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15144439	CV759162	single nucleotide variant	NM_153021.5(PLB1):c.468+8T>G	not provided [RCV000922368]	likely benign	2	28529787	28529787	Human		name
15122521	CV778931	single nucleotide variant	NM_153021.5(PLB1):c.775-2A>C	not provided [RCV000963086]	likely benign	2	28541705	28541705	Human		name
9687137	CV171345	single nucleotide variant	NM_153021.5(PLB1):c.3195+7C>A	Prostate cancer [RCV000149356]	uncertain significance	2	28614103	28614103	Human	2	name
15163777	CV743938	single nucleotide variant	NM_153021.5(PLB1):c.2856+1G>A	not provided [RCV000903850]	likely benign	2	28604048	28604048	Human		name
15130158	CV743945	single nucleotide variant	NM_153021.5(PLB1):c.3316-4A>G	not provided [RCV000897559]	likely benign	2	28620261	28620261	Human		name
15156097	CV759116	single nucleotide variant	NM_153021.5(PLB1):c.3528-9C>T	not provided [RCV000924599]	likely benign	2	28625048	28625048	Human		name
15199475	CV774744	single nucleotide variant	NM_153021.5(PLB1):c.2322-8C>T	not provided [RCV000935115]	likely benign	2	28597997	28597997	Human		name
15196151	CV774804	single nucleotide variant	NM_153021.5(PLB1):c.2248-5C>T	not provided [RCV000934140]	likely benign	2	28593676	28593676	Human		name
15151990	CV730136	single nucleotide variant	NM_153021.5(PLB1):c.2189-10G>A	not provided [RCV000879714]	benign	2	28592651	28592651	Human		name
15158608	CV730137	single nucleotide variant	NM_153021.5(PLB1):c.3661-10T>C	not provided [RCV000881040]	benign	2	28628553	28628553	Human		name
15183538	CV777202	single nucleotide variant	NM_153021.5(PLB1):c.1433+10G>A	not provided [RCV000952488]	benign	2	28573315	28573315	Human		name
405657165	CV3376217	single nucleotide variant	NM_153021.5(PLB1):c.11G>A (p.Arg4Gln)	not specified [RCV004511688]	likely benign	2	28496125	28496125	Human		name
407518725	CV3470837	single nucleotide variant	NM_153021.5(PLB1):c.92C>T (p.Thr31Ile)	not specified [RCV004651104]	uncertain significance	2	28516844	28516844	Human		name
617151204	CV4021821	single nucleotide variant	NM_153021.5(PLB1):c.792C>G (p.Leu264=)	not provided [RCV005426782]	likely benign	2	28541724	28541724	Human		name
15098756	CV719828	single nucleotide variant	NM_153021.5(PLB1):c.390G>A (p.Lys130=)	not provided [RCV000891811]	likely benign	2	28529381	28529381	Human		name
15201604	CV719829	single nucleotide variant	NM_153021.5(PLB1):c.981C>T (p.His327=)	not provided [RCV000891238]	likely benign	2	28548904	28548904	Human		name
15162557	CV733430	single nucleotide variant	NM_153021.5(PLB1):c.414T>C (p.Ala138=)	not provided [RCV000903577]	benign\|likely benign	2	28529405	28529405	Human		name
15178772	CV733431	single nucleotide variant	NM_153021.5(PLB1):c.537G>A (p.Leu179=)	not provided [RCV000906952]	likely benign	2	28532176	28532176	Human		name
156340625	CV2268149	single nucleotide variant	NM_153021.5(PLB1):c.161G>C (p.Gly54Ala)	not specified [RCV004138468]	uncertain significance	2	28518509	28518509	Human		name
405657175	CV3376220	single nucleotide variant	NM_153021.5(PLB1):c.142T>C (p.Cys48Arg)	not specified [RCV004511691]	uncertain significance	2	28518490	28518490	Human		name
407518700	CV3470825	single nucleotide variant	NM_153021.5(PLB1):c.251A>C (p.Asp84Ala)	not specified [RCV004651095]	uncertain significance	2	28525274	28525274	Human		name
15203215	CV697534	single nucleotide variant	NM_153021.5(PLB1):c.1536C>T (p.Gly512=)	not provided [RCV000958287]	benign\|likely benign	2	28579677	28579677	Human		name
15174591	CV697535	single nucleotide variant	NM_153021.5(PLB1):c.2868C>T (p.Arg956=)	not provided [RCV000950379]	benign	2	28604666	28604666	Human		name
15183566	CV708217	single nucleotide variant	NM_153021.5(PLB1):c.2097G>A (p.Pro699=)	not provided [RCV000974906]	benign	2	28591141	28591141	Human		name
15157446	CV733432	single nucleotide variant	NM_153021.5(PLB1):c.2334C>T (p.Asp778=)	not provided [RCV000902530]	benign	2	28598017	28598017	Human		name
15111377	CV747566	single nucleotide variant	NM_153021.5(PLB1):c.275A>G (p.Lys92Arg)	not provided [RCV000916719]	benign	2	28525298	28525298	Human		name
15157812	CV747567	single nucleotide variant	NM_153021.5(PLB1):c.2571C>T (p.Ile857=)	not provided [RCV000924939]	benign	2	28601296	28601296	Human		name
15124475	CV781297	single nucleotide variant	NM_153021.5(PLB1):c.2979G>A (p.Thr993=)	not provided [RCV000980013]	likely benign	2	28605870	28605870	Human		name
156186909	CV2236294	single nucleotide variant	NM_153021.5(PLB1):c.433G>T (p.Ala145Ser)	not specified [RCV004107991]	uncertain significance	2	28529744	28529744	Human		name
156219019	CV2254008	single nucleotide variant	NM_153021.5(PLB1):c.335A>T (p.Asp112Val)	not specified [RCV004129464]	uncertain significance	2	28529326	28529326	Human		name
156248899	CV2264030	single nucleotide variant	NM_153021.5(PLB1):c.860C>G (p.Thr287Ser)	not specified [RCV004138049]	uncertain significance	2	28541792	28541792	Human		name
155943295	CV2298502	single nucleotide variant	NM_153021.5(PLB1):c.568G>T (p.Ala190Ser)	not specified [RCV004162166]	uncertain significance	2	28538331	28538331	Human		name
155970384	CV2335577	single nucleotide variant	NM_153021.5(PLB1):c.740G>A (p.Arg247Gln)	not specified [RCV004193785]	uncertain significance	2	28540407	28540407	Human		name
155985996	CV2345443	single nucleotide variant	NM_153021.5(PLB1):c.878C>T (p.Ser293Leu)	not specified [RCV004198215]	uncertain significance	2	28541810	28541810	Human		name
156338527	CV2370668	single nucleotide variant	NM_153021.5(PLB1):c.779C>T (p.Ala260Val)	not specified [RCV004209076]	uncertain significance	2	28541711	28541711	Human		name
156062021	CV2392067	single nucleotide variant	NM_153021.5(PLB1):c.884A>T (p.Asp295Val)	not specified [RCV004237962]	uncertain significance	2	28543216	28543216	Human		name
329391878	CV2445094	single nucleotide variant	NM_153021.5(PLB1):c.685G>A (p.Gly229Ser)	not specified [RCV004261698]	uncertain significance	2	28539165	28539165	Human		name
401753685	CV2685025	single nucleotide variant	NM_153021.5(PLB1):c.574G>A (p.Gly192Ser)	not specified [RCV004289608]	likely benign	2	28538337	28538337	Human		name
401737762	CV2699911	single nucleotide variant	NM_153021.5(PLB1):c.804C>A (p.Ser268Arg)	not specified [RCV004308542]	uncertain significance	2	28541736	28541736	Human		name
401732636	CV2708916	single nucleotide variant	NM_153021.5(PLB1):c.304G>A (p.Val102Met)	not specified [RCV004309884]	uncertain significance	2	28525924	28525924	Human		name
401863206	CV2771910	single nucleotide variant	NM_153021.5(PLB1):c.569C>T (p.Ala190Val)	not specified [RCV004344617]	uncertain significance	2	28538332	28538332	Human		name
405657211	CV3376231	single nucleotide variant	NM_153021.5(PLB1):c.3510G>A (p.Ala1170=)	not specified [RCV004511702]	likely benign	2	28620961	28620961	Human		name
405657226	CV3376236	single nucleotide variant	NM_153021.5(PLB1):c.488A>T (p.Asp163Val)	not specified [RCV004511707]	uncertain significance	2	28532127	28532127	Human		name
405657229	CV3376237	single nucleotide variant	NM_153021.5(PLB1):c.515G>A (p.Ser172Asn)	not specified [RCV004511708]	uncertain significance	2	28532154	28532154	Human		name
405657232	CV3376238	single nucleotide variant	NM_153021.5(PLB1):c.580G>A (p.Asp194Asn)	not specified [RCV004511709]	uncertain significance	2	28538343	28538343	Human		name
405657236	CV3376239	single nucleotide variant	NM_153021.5(PLB1):c.608T>C (p.Leu203Pro)	not specified [RCV004511710]	uncertain significance	2	28538371	28538371	Human		name
405657240	CV3376240	single nucleotide variant	NM_153021.5(PLB1):c.706C>A (p.Pro236Thr)	not specified [RCV004511711]	uncertain significance	2	28540373	28540373	Human		name
405657246	CV3376242	single nucleotide variant	NM_153021.5(PLB1):c.976A>C (p.Lys326Gln)	not specified [RCV004511713]	uncertain significance	2	28548899	28548899	Human		name
407470319	CV3470827	single nucleotide variant	NM_153021.5(PLB1):c.860C>A (p.Thr287Asn)	not specified [RCV004662013]	uncertain significance	2	28541792	28541792	Human		name
407518703	CV3470828	single nucleotide variant	NM_153021.5(PLB1):c.890G>A (p.Arg297Gln)	not specified [RCV004651096]	uncertain significance	2	28543222	28543222	Human		name
407518716	CV3470834	single nucleotide variant	NM_153021.5(PLB1):c.704C>A (p.Ala235Glu)	not specified [RCV004651101]	uncertain significance	2	28540371	28540371	Human		name
407518719	CV3470835	single nucleotide variant	NM_153021.5(PLB1):c.331T>C (p.Ser111Pro)	not specified [RCV004651102]	uncertain significance	2	28529322	28529322	Human		name
597726193	CV3579798	single nucleotide variant	NM_153021.5(PLB1):c.539G>A (p.Cys180Tyr)	not specified [RCV004842399]	uncertain significance	2	28532178	28532178	Human		name
597726206	CV3579800	single nucleotide variant	NM_153021.5(PLB1):c.482A>C (p.Gln161Pro)	not specified [RCV004842401]	uncertain significance	2	28532121	28532121	Human		name
598206074	CV4000362	single nucleotide variant	NM_153021.5(PLB1):c.844C>T (p.Pro282Ser)	not specified [RCV005399568]	uncertain significance	2	28541776	28541776	Human		name
598206092	CV4000365	single nucleotide variant	NM_153021.5(PLB1):c.733A>G (p.Thr245Ala)	not specified [RCV005399571]	uncertain significance	2	28540400	28540400	Human		name
598206118	CV4000369	single nucleotide variant	NM_153021.5(PLB1):c.510C>A (p.Phe170Leu)	not specified [RCV005399575]	uncertain significance	2	28532149	28532149	Human		name
598206123	CV4000370	single nucleotide variant	NM_153021.5(PLB1):c.854A>G (p.Tyr285Cys)	not specified [RCV005399576]	uncertain significance	2	28541786	28541786	Human		name
598206142	CV4000373	single nucleotide variant	NM_153021.5(PLB1):c.458A>G (p.Lys153Arg)	not specified [RCV005399579]	uncertain significance	2	28529769	28529769	Human		name
598206147	CV4000374	single nucleotide variant	NM_153021.5(PLB1):c.551A>G (p.Gln184Arg)	not specified [RCV005399580]	uncertain significance	2	28532190	28532190	Human		name
598206212	CV4000385	single nucleotide variant	NM_153021.5(PLB1):c.406G>A (p.Asp136Asn)	not specified [RCV005399591]	uncertain significance	2	28529397	28529397	Human		name
15155949	CV697532	single nucleotide variant	NM_153021.5(PLB1):c.445G>T (p.Val149Leu)	not provided [RCV000946597]	benign	2	28529756	28529756	Human		name
15153418	CV708221	single nucleotide variant	NM_153021.5(PLB1):c.3747C>T (p.Asn1249=)	not provided [RCV000968540]	likely benign	2	28629114	28629114	Human		name
156365722	CV2193260	single nucleotide variant	NM_153021.5(PLB1):c.2974G>T (p.Asp992Tyr)	not specified [RCV004071243]	uncertain significance	2	28605865	28605865	Human		name
156324683	CV2198833	single nucleotide variant	NM_153021.5(PLB1):c.2944C>A (p.Gln982Lys)	not provided [RCV004695351]\|not specified [RCV004077872]	uncertain significance	2	28604742	28604742	Human		name
155922201	CV2207432	single nucleotide variant	NM_153021.5(PLB1):c.2581G>A (p.Asp861Asn)	not specified [RCV004088128]	uncertain significance	2	28601306	28601306	Human		name
155981708	CV2208489	single nucleotide variant	NM_153021.5(PLB1):c.1538A>G (p.Asn513Ser)	not specified [RCV004091022]	uncertain significance	2	28579679	28579679	Human		name
156128672	CV2220065	single nucleotide variant	NM_153021.5(PLB1):c.2332G>C (p.Asp778His)	not specified [RCV004093941]	uncertain significance	2	28598015	28598015	Human		name
156071219	CV2229137	single nucleotide variant	NM_153021.5(PLB1):c.2891A>G (p.Tyr964Cys)	not specified [RCV004099183]	uncertain significance	2	28604689	28604689	Human		name
156129432	CV2238535	single nucleotide variant	NM_153021.5(PLB1):c.2280C>A (p.Asp760Glu)	not specified [RCV004107151]	uncertain significance	2	28593713	28593713	Human		name
156025930	CV2274028	single nucleotide variant	NM_153021.5(PLB1):c.2538C>A (p.Phe846Leu)	not specified [RCV004134412]	uncertain significance	2	28601263	28601263	Human		name
155994612	CV2277994	single nucleotide variant	NM_153021.5(PLB1):c.2426A>G (p.Asn809Ser)	not specified [RCV004141231]	likely benign	2	28598712	28598712	Human		name
156280884	CV2281797	single nucleotide variant	NM_153021.5(PLB1):c.2511G>T (p.Lys837Asn)	not specified [RCV004147930]	uncertain significance	2	28600845	28600845	Human		name
156268752	CV2293059	single nucleotide variant	NM_153021.5(PLB1):c.2098T>C (p.Phe700Leu)	not specified [RCV004148808]	uncertain significance	2	28591142	28591142	Human		name
156015779	CV2298974	single nucleotide variant	NM_153021.5(PLB1):c.2407G>T (p.Val803Leu)	not specified [RCV004158503]	uncertain significance	2	28598693	28598693	Human		name
156300700	CV2306987	single nucleotide variant	NM_153021.5(PLB1):c.1256C>G (p.Thr419Ser)	not specified [RCV004157496]	uncertain significance	2	28565329	28565329	Human		name
156271859	CV2308664	single nucleotide variant	NM_153021.5(PLB1):c.1919C>T (p.Ser640Leu)	not specified [RCV004167214]	uncertain significance	2	28589553	28589553	Human		name
155926347	CV2365738	single nucleotide variant	NM_153021.5(PLB1):c.2567T>G (p.Leu856Arg)	not specified [RCV004214280]	uncertain significance	2	28601292	28601292	Human		name
155954079	CV2379137	single nucleotide variant	NM_153021.5(PLB1):c.1951C>T (p.Pro651Ser)	not specified [RCV004235931]	uncertain significance	2	28589705	28589705	Human		name
156181758	CV2384105	single nucleotide variant	NM_153021.5(PLB1):c.2981C>G (p.Ser994Cys)	not specified [RCV004227511]	uncertain significance	2	28605872	28605872	Human		name
155939489	CV2385681	single nucleotide variant	NM_153021.5(PLB1):c.1133C>T (p.Thr378Met)	not specified [RCV004233309]	uncertain significance	2	28552977	28552977	Human		name
155956527	CV2387308	single nucleotide variant	NM_153021.5(PLB1):c.1822A>T (p.Thr608Ser)	not specified [RCV004238396]	uncertain significance	2	28589456	28589456	Human		name
156006153	CV2394125	single nucleotide variant	NM_153021.5(PLB1):c.2414C>T (p.Thr805Met)	not specified [RCV004236328]	uncertain significance	2	28598700	28598700	Human		name
156006220	CV2394137	single nucleotide variant	NM_153021.5(PLB1):c.1249G>A (p.Val417Ile)	not specified [RCV004236337]	uncertain significance	2	28565322	28565322	Human		name
156189191	CV2395627	single nucleotide variant	NM_153021.5(PLB1):c.1282G>C (p.Val428Leu)	not specified [RCV004241471]	uncertain significance	2	28566797	28566797	Human		name
155999139	CV2396368	single nucleotide variant	NM_153021.5(PLB1):c.2299C>G (p.Gln767Glu)	not specified [RCV004242091]	uncertain significance	2	28593732	28593732	Human		name
156044983	CV2397178	single nucleotide variant	NM_153021.5(PLB1):c.2458C>G (p.Pro820Ala)	not specified [RCV004238718]	uncertain significance	2	28598744	28598744	Human		name
329369728	CV2424894	single nucleotide variant	NM_153021.5(PLB1):c.1774A>G (p.Thr592Ala)	not specified [RCV004248777]	uncertain significance	2	28585801	28585801	Human		name
329368423	CV2428014	single nucleotide variant	NM_153021.5(PLB1):c.2305C>T (p.Arg769Trp)	not specified [RCV004254393]	uncertain significance	2	28593738	28593738	Human		name
329374915	CV2440121	single nucleotide variant	NM_153021.5(PLB1):c.1498C>A (p.Gln500Lys)	not specified [RCV004260585]	uncertain significance	2	28579639	28579639	Human		name
329386398	CV2455914	single nucleotide variant	NM_153021.5(PLB1):c.2423C>G (p.Ala808Gly)	not specified [RCV004279185]	uncertain significance	2	28598709	28598709	Human		name
329378830	CV2459980	single nucleotide variant	NM_153021.5(PLB1):c.1738C>G (p.Leu580Val)	not specified [RCV004279456]	uncertain significance	2	28585765	28585765	Human		name
401742967	CV2677728	single nucleotide variant	NM_153021.5(PLB1):c.2854C>T (p.Arg952Trp)	not specified [RCV004291807]	uncertain significance	2	28604045	28604045	Human		name
401740450	CV2684361	single nucleotide variant	NM_153021.5(PLB1):c.2975A>G (p.Asp992Gly)	not specified [RCV004289007]	uncertain significance	2	28605866	28605866	Human		name
401734282	CV2688457	single nucleotide variant	NM_153021.5(PLB1):c.1693T>A (p.Tyr565Asn)	not specified [RCV004301437]	uncertain significance	2	28582465	28582465	Human		name
401781895	CV2689987	single nucleotide variant	NM_153021.5(PLB1):c.1792A>G (p.Ile598Val)	not specified [RCV004299871]	uncertain significance	2	28585819	28585819	Human		name
401760056	CV2701858	single nucleotide variant	NM_153021.5(PLB1):c.1180A>G (p.Ile394Val)	not specified [RCV004307822]	uncertain significance	2	28563073	28563073	Human		name
401752240	CV2710652	single nucleotide variant	NM_153021.5(PLB1):c.2023C>G (p.Pro675Ala)	not specified [RCV004319562]	uncertain significance	2	28590011	28590011	Human		name
401765266	CV2712586	single nucleotide variant	NM_153021.5(PLB1):c.1322C>A (p.Ala441Glu)	not specified [RCV004307916]	uncertain significance	2	28566837	28566837	Human		name
401751363	CV2716365	single nucleotide variant	NM_153021.5(PLB1):c.1279A>T (p.Ser427Cys)	not specified [RCV004325359]	uncertain significance	2	28565352	28565352	Human		name
401729720	CV2733273	single nucleotide variant	NM_153021.5(PLB1):c.2514G>T (p.Met838Ile)	not specified [RCV004332184]	uncertain significance	2	28600848	28600848	Human		name
401892943	CV2758281	single nucleotide variant	NM_153021.5(PLB1):c.1177G>A (p.Val393Ile)	not specified [RCV004341638]	uncertain significance	2	28563070	28563070	Human		name
401857407	CV2760144	single nucleotide variant	NM_153021.5(PLB1):c.2606C>T (p.Ser869Leu)	not specified [RCV004347327]	uncertain significance	2	28601331	28601331	Human		name
401862590	CV2762250	single nucleotide variant	NM_153021.5(PLB1):c.2587T>C (p.Cys863Arg)	not specified [RCV004335374]	uncertain significance	2	28601312	28601312	Human		name
401858505	CV2774326	single nucleotide variant	NM_153021.5(PLB1):c.1576T>C (p.Ser526Pro)	not specified [RCV004347679]	uncertain significance	2	28582077	28582077	Human		name
401865724	CV2786106	single nucleotide variant	NM_153021.5(PLB1):c.2278G>A (p.Asp760Asn)	not specified [RCV004359916]	uncertain significance	2	28593711	28593711	Human		name
401910905	CV2815637	single nucleotide variant	NM_153021.5(PLB1):c.1708G>A (p.Val570Ile)	not provided [RCV003425551]	likely benign	2	28582480	28582480	Human		name
405657168	CV3376218	single nucleotide variant	NM_153021.5(PLB1):c.1418C>T (p.Ala473Val)	not specified [RCV004511689]	uncertain significance	2	28573290	28573290	Human		name
405657179	CV3376221	single nucleotide variant	NM_153021.5(PLB1):c.1553T>C (p.Phe518Ser)	not specified [RCV004511692]	uncertain significance	2	28579694	28579694	Human		name
405657183	CV3376222	single nucleotide variant	NM_153021.5(PLB1):c.1828C>G (p.Gln610Glu)	not specified [RCV004511693]	uncertain significance	2	28589462	28589462	Human		name
405657187	CV3376223	single nucleotide variant	NM_153021.5(PLB1):c.1997G>A (p.Ser666Asn)	not specified [RCV004511694]	uncertain significance	2	28589751	28589751	Human		name
405657189	CV3376224	single nucleotide variant	NM_153021.5(PLB1):c.2026G>T (p.Val676Phe)	not specified [RCV004511695]	uncertain significance	2	28590014	28590014	Human		name
405657193	CV3376225	single nucleotide variant	NM_153021.5(PLB1):c.2056G>A (p.Glu686Lys)	not specified [RCV004511696]	uncertain significance	2	28590044	28590044	Human		name
405657196	CV3376226	single nucleotide variant	NM_153021.5(PLB1):c.2441T>C (p.Phe814Ser)	not specified [RCV004511697]	uncertain significance	2	28598727	28598727	Human		name
405657202	CV3376228	single nucleotide variant	NM_153021.5(PLB1):c.2887C>G (p.Arg963Gly)	not specified [RCV004511699]	uncertain significance	2	28604685	28604685	Human		name
407470315	CV3470826	single nucleotide variant	NM_153021.5(PLB1):c.1399T>C (p.Phe467Leu)	not specified [RCV004662012]	uncertain significance	2	28573271	28573271	Human		name
407518709	CV3470830	single nucleotide variant	NM_153021.5(PLB1):c.2726G>A (p.Arg909Gln)	not specified [RCV004651098]	uncertain significance	2	28602873	28602873	Human		name
407518712	CV3470831	single nucleotide variant	NM_153021.5(PLB1):c.1651A>G (p.Asn551Asp)	not specified [RCV004651099]	uncertain significance	2	28582423	28582423	Human		name
407518722	CV3470836	single nucleotide variant	NM_153021.5(PLB1):c.1201C>T (p.Leu401Phe)	not specified [RCV004651103]	uncertain significance	2	28563094	28563094	Human		name
597726213	CV3579801	single nucleotide variant	NM_153021.5(PLB1):c.2353A>T (p.Thr785Ser)	not specified [RCV004842402]	uncertain significance	2	28598036	28598036	Human		name
597767859	CV3579804	single nucleotide variant	NM_153021.5(PLB1):c.1497T>A (p.Phe499Leu)	not specified [RCV004850570]	uncertain significance	2	28579638	28579638	Human		name
597726236	CV3579805	single nucleotide variant	NM_153021.5(PLB1):c.1772C>T (p.Ser591Leu)	not specified [RCV004842405]	uncertain significance	2	28585799	28585799	Human		name
597726242	CV3579806	single nucleotide variant	NM_153021.5(PLB1):c.2624C>A (p.Ala875Asp)	not specified [RCV004842406]	uncertain significance	2	28601915	28601915	Human		name
597726264	CV3579809	single nucleotide variant	NM_153021.5(PLB1):c.2849C>A (p.Ala950Asp)	not specified [RCV004842409]	uncertain significance	2	28604040	28604040	Human		name
597767864	CV3579810	single nucleotide variant	NM_153021.5(PLB1):c.2057A>G (p.Glu686Gly)	not specified [RCV004850571]	uncertain significance	2	28590045	28590045	Human		name
597726272	CV3579811	single nucleotide variant	NM_153021.5(PLB1):c.1115A>G (p.Asp372Gly)	not specified [RCV004842410]	uncertain significance	2	28552959	28552959	Human		name
597767869	CV3579812	single nucleotide variant	NM_153021.5(PLB1):c.1847G>A (p.Arg616Gln)	not specified [RCV004850572]	uncertain significance	2	28589481	28589481	Human		name
597767874	CV3579813	single nucleotide variant	NM_153021.5(PLB1):c.2061C>G (p.Asn687Lys)	not specified [RCV004850573]	uncertain significance	2	28590049	28590049	Human		name
597726279	CV3579814	single nucleotide variant	NM_153021.5(PLB1):c.2846G>A (p.Arg949Gln)	not specified [RCV004842411]	likely benign	2	28604037	28604037	Human		name
597726287	CV3579815	single nucleotide variant	NM_153021.5(PLB1):c.2000C>T (p.Ala667Val)	not specified [RCV004842412]	uncertain significance	2	28589754	28589754	Human		name
598206035	CV4000355	single nucleotide variant	NM_153021.5(PLB1):c.2910C>A (p.Phe970Leu)	not specified [RCV005399561]	uncertain significance	2	28604708	28604708	Human		name
598206080	CV4000363	single nucleotide variant	NM_153021.5(PLB1):c.2730G>C (p.Gln910His)	not specified [RCV005399569]	uncertain significance	2	28602877	28602877	Human		name
598206086	CV4000364	single nucleotide variant	NM_153021.5(PLB1):c.2147C>T (p.Pro716Leu)	not specified [RCV005399570]	likely benign	2	28591719	28591719	Human		name
598206099	CV4000366	single nucleotide variant	NM_153021.5(PLB1):c.2015T>C (p.Met672Thr)	not specified [RCV005399572]	uncertain significance	2	28589769	28589769	Human		name
598206130	CV4000371	single nucleotide variant	NM_153021.5(PLB1):c.1825C>T (p.His609Tyr)	not specified [RCV005399577]	uncertain significance	2	28589459	28589459	Human		name
598206136	CV4000372	single nucleotide variant	NM_153021.5(PLB1):c.1535G>T (p.Gly512Val)	not specified [RCV005399578]	uncertain significance	2	28579676	28579676	Human		name
598206162	CV4000376	single nucleotide variant	NM_153021.5(PLB1):c.2888G>A (p.Arg963His)	not specified [RCV005399582]	uncertain significance	2	28604686	28604686	Human		name
598206174	CV4000378	single nucleotide variant	NM_153021.5(PLB1):c.1561G>T (p.Asp521Tyr)	not specified [RCV005399584]	uncertain significance	2	28579702	28579702	Human		name
598206195	CV4000382	single nucleotide variant	NM_153021.5(PLB1):c.1988G>A (p.Arg663Gln)	not specified [RCV005399588]	uncertain significance	2	28589742	28589742	Human		name
598206201	CV4000383	single nucleotide variant	NM_153021.5(PLB1):c.2978C>T (p.Thr993Met)	not specified [RCV005399589]	uncertain significance	2	28605869	28605869	Human		name
15155955	CV697533	single nucleotide variant	NM_153021.5(PLB1):c.1019A>G (p.Tyr340Cys)	not provided [RCV000946598]	benign	2	28550020	28550020	Human		name
15177589	CV708214	single nucleotide variant	NM_153021.5(PLB1):c.1675G>A (p.Val559Ile)	not provided [RCV000973465]	benign	2	28582447	28582447	Human		name
15167790	CV708215	single nucleotide variant	NM_153021.5(PLB1):c.2039C>T (p.Thr680Met)	not provided [RCV000971474]	benign	2	28590027	28590027	Human		name
15167797	CV708216	single nucleotide variant	NM_153021.5(PLB1):c.2094G>C (p.Gln698His)	not provided [RCV000971475]	benign	2	28591138	28591138	Human		name
15115960	CV708218	single nucleotide variant	NM_153021.5(PLB1):c.2435A>T (p.Asn812Ile)	not provided [RCV000961947]	benign	2	28598721	28598721	Human		name
15167802	CV708219	single nucleotide variant	NM_153021.5(PLB1):c.2461G>A (p.Gly821Arg)	not provided [RCV000971476]	benign	2	28598747	28598747	Human		name
15176133	CV708220	single nucleotide variant	NM_153021.5(PLB1):c.2710A>T (p.Asn904Tyr)	not provided [RCV000973116]	benign	2	28602857	28602857	Human		name
15171211	CV719830	single nucleotide variant	NM_153021.5(PLB1):c.2045G>A (p.Arg682His)	not provided [RCV000883612]	likely benign	2	28590033	28590033	Human		name
15199576	CV719831	single nucleotide variant	NM_153021.5(PLB1):c.2432C>T (p.Thr811Met)	not provided [RCV000890671]	likely benign	2	28598718	28598718	Human		name
15199579	CV719832	single nucleotide variant	NM_153021.5(PLB1):c.2644C>T (p.Arg882Cys)	not provided [RCV000890672]	benign	2	28601935	28601935	Human		name
15194721	CV719833	single nucleotide variant	NM_153021.5(PLB1):c.2645G>A (p.Arg882His)	not provided [RCV000889298]	benign	2	28601936	28601936	Human		name
15113846	CV747568	single nucleotide variant	NM_153021.5(PLB1):c.2576G>A (p.Gly859Asp)	not provided [RCV000917170]	likely benign	2	28601301	28601301	Human		name
156132632	CV2206654	single nucleotide variant	NM_153021.5(PLB1):c.3170C>T (p.Thr1057Met)	not specified [RCV004080992]	uncertain significance	2	28614071	28614071	Human		name
156026833	CV2242392	single nucleotide variant	NM_153021.5(PLB1):c.4114C>T (p.Arg1372Cys)	not specified [RCV004111392]	uncertain significance	2	28640942	28640942	Human		name
156287617	CV2301258	single nucleotide variant	NM_153021.5(PLB1):c.3517G>A (p.Ala1173Thr)	not specified [RCV004160439]	uncertain significance	2	28620968	28620968	Human		name
156173640	CV2333733	single nucleotide variant	NM_153021.5(PLB1):c.3662A>C (p.Glu1221Ala)	not specified [RCV004181246]	uncertain significance	2	28628564	28628564	Human		name
155922081	CV2350768	single nucleotide variant	NM_153021.5(PLB1):c.4057C>A (p.Arg1353Ser)	not specified [RCV004207105]	uncertain significance	2	28632998	28632998	Human		name
156169803	CV2354815	single nucleotide variant	NM_153021.5(PLB1):c.3322G>C (p.Val1108Leu)	not specified [RCV004198342]	uncertain significance	2	28620271	28620271	Human		name
156402619	CV2361827	single nucleotide variant	NM_153021.5(PLB1):c.3386T>C (p.Ile1129Thr)	not specified [RCV004223298]	uncertain significance	2	28620602	28620602	Human		name
156264252	CV2384597	single nucleotide variant	NM_153021.5(PLB1):c.3694A>C (p.Ile1232Leu)	not specified [RCV004232382]	uncertain significance	2	28628596	28628596	Human		name
155954700	CV2389806	single nucleotide variant	NM_153021.5(PLB1):c.4123A>G (p.Thr1375Ala)	not specified [RCV004236032]	uncertain significance	2	28640951	28640951	Human		name
155907499	CV2389897	single nucleotide variant	NM_153021.5(PLB1):c.3295G>A (p.Ala1099Thr)	not specified [RCV004236108]	uncertain significance	2	28618379	28618379	Human		name
156150336	CV2394644	single nucleotide variant	NM_153021.5(PLB1):c.3932A>C (p.Tyr1311Ser)	not specified [RCV004240984]	uncertain significance	2	28632070	28632070	Human		name
329400495	CV2438401	single nucleotide variant	NM_153021.5(PLB1):c.3500A>C (p.Asn1167Thr)	not specified [RCV004259558]	uncertain significance	2	28620951	28620951	Human		name
401777020	CV2721572	single nucleotide variant	NM_153021.5(PLB1):c.4340A>C (p.Glu1447Ala)	not specified [RCV004316082]	uncertain significance	2	28643024	28643024	Human		name
401878621	CV2754719	single nucleotide variant	NM_153021.5(PLB1):c.3845C>T (p.Ser1282Leu)	not specified [RCV004339387]	uncertain significance	2	28630612	28630612	Human		name
401891550	CV2780531	single nucleotide variant	NM_153021.5(PLB1):c.3611T>C (p.Val1204Ala)	not specified [RCV004358218]	uncertain significance	2	28626459	28626459	Human		name
401910906	CV2815638	single nucleotide variant	NM_153021.5(PLB1):c.3133G>A (p.Glu1045Lys)	not provided [RCV003425552]	benign	2	28614034	28614034	Human		name
404981317	CV2850803	single nucleotide variant	NM_153021.5(PLB1):c.3940C>T (p.Arg1314Cys)	not provided [RCV003488268]	uncertain significance	2	28632078	28632078	Human		name
405657205	CV3376229	single nucleotide variant	NM_153021.5(PLB1):c.3155G>A (p.Arg1052Gln)	not specified [RCV004511700]	uncertain significance	2	28614056	28614056	Human		name
405657208	CV3376230	single nucleotide variant	NM_153021.5(PLB1):c.3277G>A (p.Asp1093Asn)	not specified [RCV004511701]	uncertain significance	2	28618361	28618361	Human		name
405657213	CV3376232	single nucleotide variant	NM_153021.5(PLB1):c.3742G>A (p.Val1248Ile)	not specified [RCV004511703]	likely benign	2	28629109	28629109	Human		name
405657217	CV3376233	single nucleotide variant	NM_153021.5(PLB1):c.3904A>T (p.Ile1302Phe)	not specified [RCV004511704]	uncertain significance	2	28632042	28632042	Human		name
405657220	CV3376234	single nucleotide variant	NM_153021.5(PLB1):c.3935C>T (p.Thr1312Ile)	not specified [RCV004511705]	uncertain significance	2	28632073	28632073	Human		name
405657224	CV3376235	single nucleotide variant	NM_153021.5(PLB1):c.4060G>A (p.Gly1354Arg)	not specified [RCV004511706]	uncertain significance	2	28633001	28633001	Human		name
407518697	CV3470824	single nucleotide variant	NM_153021.5(PLB1):c.4058G>A (p.Arg1353His)	not specified [RCV004651094]	uncertain significance	2	28632999	28632999	Human		name
407518706	CV3470829	single nucleotide variant	NM_153021.5(PLB1):c.3659C>T (p.Pro1220Leu)	not specified [RCV004651097]	uncertain significance	2	28626507	28626507	Human		name
407470322	CV3470832	single nucleotide variant	NM_153021.5(PLB1):c.3068T>C (p.Leu1023Pro)	not specified [RCV004662014]	uncertain significance	2	28606506	28606506	Human		name
407518715	CV3470833	single nucleotide variant	NM_153021.5(PLB1):c.3353T>A (p.Leu1118Gln)	not specified [RCV004651100]	uncertain significance	2	28620302	28620302	Human		name
597726179	CV3579796	single nucleotide variant	NM_153021.5(PLB1):c.3819G>C (p.Gln1273His)	not specified [RCV004842397]	uncertain significance	2	28630586	28630586	Human		name
597726186	CV3579797	single nucleotide variant	NM_153021.5(PLB1):c.3793G>A (p.Gly1265Arg)	not specified [RCV004842398]	uncertain significance	2	28629160	28629160	Human		name
597726221	CV3579802	single nucleotide variant	NM_153021.5(PLB1):c.4039T>C (p.Cys1347Arg)	not specified [RCV004842403]	uncertain significance	2	28632980	28632980	Human		name
597726228	CV3579803	single nucleotide variant	NM_153021.5(PLB1):c.3748G>A (p.Val1250Met)	not specified [RCV004842404]	uncertain significance	2	28629115	28629115	Human		name
597726249	CV3579807	single nucleotide variant	NM_153021.5(PLB1):c.3652G>A (p.Glu1218Lys)	not specified [RCV004842407]	uncertain significance	2	28626500	28626500	Human		name
598206029	CV4000354	single nucleotide variant	NM_153021.5(PLB1):c.4271C>T (p.Ala1424Val)	not specified [RCV005399560]	uncertain significance	2	28642955	28642955	Human		name
598206040	CV4000356	single nucleotide variant	NM_153021.5(PLB1):c.4258G>A (p.Val1420Ile)	not specified [RCV005399562]	uncertain significance	2	28642942	28642942	Human		name
598206045	CV4000357	single nucleotide variant	NM_153021.5(PLB1):c.3623T>C (p.Ile1208Thr)	not specified [RCV005399563]	uncertain significance	2	28626471	28626471	Human		name
598206056	CV4000359	single nucleotide variant	NM_153021.5(PLB1):c.3271C>A (p.Pro1091Thr)	not specified [RCV005399565]	uncertain significance	2	28618355	28618355	Human		name
598206062	CV4000360	single nucleotide variant	NM_153021.5(PLB1):c.4279G>A (p.Gly1427Ser)	not specified [RCV005399566]	uncertain significance	2	28642963	28642963	Human		name
598206068	CV4000361	single nucleotide variant	NM_153021.5(PLB1):c.3610G>T (p.Val1204Phe)	not specified [RCV005399567]	uncertain significance	2	28626458	28626458	Human		name
598206106	CV4000367	single nucleotide variant	NM_153021.5(PLB1):c.3466T>A (p.Ser1156Thr)	not specified [RCV005399573]	uncertain significance	2	28620917	28620917	Human		name
598206153	CV4000375	single nucleotide variant	NM_153021.5(PLB1):c.3988A>T (p.Thr1330Ser)	not specified [RCV005399581]	uncertain significance	2	28632126	28632126	Human		name
598206167	CV4000377	single nucleotide variant	NM_153021.5(PLB1):c.3391G>A (p.Gly1131Arg)	not specified [RCV005399583]	uncertain significance	2	28620607	28620607	Human		name
598206206	CV4000384	single nucleotide variant	NM_153021.5(PLB1):c.3515G>C (p.Gly1172Ala)	not specified [RCV005399590]	uncertain significance	2	28620966	28620966	Human		name
598206217	CV4000386	single nucleotide variant	NM_153021.5(PLB1):c.4017C>A (p.Asp1339Glu)	not specified [RCV005399592]	uncertain significance	2	28632958	28632958	Human		name
598206224	CV4000387	single nucleotide variant	NM_153021.5(PLB1):c.3269G>A (p.Arg1090Gln)	not specified [RCV005399593]	likely benign	2	28618353	28618353	Human		name
15190255	CV719834	single nucleotide variant	NM_153021.5(PLB1):c.3978A>C (p.Gln1326His)	not provided [RCV000888049]	benign	2	28632116	28632116	Human		name
15193354	CV719835	single nucleotide variant	NM_153021.5(PLB1):c.4115G>A (p.Arg1372His)	not provided [RCV000888924]	benign	2	28640943	28640943	Human		name
15171343	CV719836	single nucleotide variant	NM_153021.5(PLB1):c.4334G>A (p.Arg1445Gln)	not provided [RCV000883636]	likely benign	2	28643018	28643018	Human		name
8625347	CV80470	single nucleotide variant	NM_001170585.1(PLB1):c.3360G>A (p.Gly1120=)	Malignant melanoma [RCV000060547]	not provided	2	28620609	28620609	Human		name
8625346	CV80469	single nucleotide variant	NM_001170585.1(PLB1):c.1919C>T (p.Pro640Leu)	Malignant melanoma [RCV000060546]	not provided	2	28589706	28589706	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message