DISP2[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2365664	NM_033510.3(DISP2):c.7G>A (p.Gly3Ser)	DISP2, LOC130056841 (G3S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082606	NM_033510.3(DISP2):c.20G>C (p.Ser7Thr)	DISP2, LOC130056841 (S7T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082610	NM_033510.3(DISP2):c.25A>G (p.Ser9Gly)	DISP2, LOC130056841 (S9G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592059	NM_033510.3(DISP2):c.43G>A (p.Ala15Thr)	DISP2, LOC130056841 (A15T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310089	NM_033510.3(DISP2):c.112C>G (p.Pro38Ala)	DISP2 (P38A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270777	NM_033510.3(DISP2):c.113C>G (p.Pro38Arg)	DISP2 (P38R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381131	NM_033510.3(DISP2):c.274C>T (p.His92Tyr)	DISP2 (H92Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082611	NM_033510.3(DISP2):c.284A>G (p.Tyr95Cys)	DISP2 (Y95C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412379	NM_033510.3(DISP2):c.289C>T (p.Arg97Trp)	DISP2 (R97W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457730	NM_033510.3(DISP2):c.299A>C (p.Gln100Pro)	DISP2 (Q100P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082613	NM_033510.3(DISP2):c.301G>C (p.Glu101Gln)	DISP2 (E101Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489085	NM_033510.3(DISP2):c.308A>C (p.Gln103Pro)	DISP2 (Q103P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2330835	NM_033510.3(DISP2):c.480C>A (p.Ser160Arg)	DISP2 (S160R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 720007	NM_033510.3(DISP2):c.582C>T (p.Pro194=)	DISP2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2306477	NM_033510.3(DISP2):c.592A>G (p.Lys198Glu)	DISP2 (K198E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082619	NM_033510.3(DISP2):c.616C>T (p.Arg206Trp)	DISP2 (R206W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2645168	NM_033510.3(DISP2):c.627C>T (p.Asp209=)	DISP2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3272172	NM_033510.3(DISP2):c.629T>C (p.Ile210Thr)	DISP2 (I210T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2645169	NM_033510.3(DISP2):c.646G>A (p.Val216Ile)	DISP2 (V216I)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3082620	NM_033510.3(DISP2):c.725G>T (p.Ser242Ile)	DISP2 (S242I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082621	NM_033510.3(DISP2):c.743G>C (p.Arg248Thr)	DISP2 (R248T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082622	NM_033510.3(DISP2):c.751C>T (p.Pro251Ser)	DISP2 (P251S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267648	NM_033510.3(DISP2):c.755G>A (p.Arg252Lys)	DISP2 (R252K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082623	NM_033510.3(DISP2):c.761G>C (p.Ser254Thr)	DISP2 (S254T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2606926	NM_033510.3(DISP2):c.775G>A (p.Ala259Thr)	DISP2 (A259T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082624	NM_033510.3(DISP2):c.781C>G (p.Arg261Gly)	DISP2 (R261G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249110	NM_033510.3(DISP2):c.782G>A (p.Arg261Gln)	DISP2 (R261Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380671	NM_033510.3(DISP2):c.787C>T (p.Arg263Trp)	DISP2 (R263W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082625	NM_033510.3(DISP2):c.788G>A (p.Arg263Gln)	DISP2 (R263Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254064	NM_033510.3(DISP2):c.869T>C (p.Val290Ala)	DISP2 (V290A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272175	NM_033510.3(DISP2):c.875T>C (p.Met292Thr)	DISP2 (M292T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333227	NM_033510.3(DISP2):c.903C>A (p.Asn301Lys)	DISP2 (N301K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218440	NM_033510.3(DISP2):c.931A>G (p.Met311Val)	DISP2 (M311V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335689	NM_033510.3(DISP2):c.988G>A (p.Ala330Thr)	DISP2 (A330T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082596	NM_033510.3(DISP2):c.1049G>A (p.Arg350His)	DISP2 (R350H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405134	NM_033510.3(DISP2):c.1097C>T (p.Ala366Val)	DISP2 (A366V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310964	NM_033510.3(DISP2):c.1114G>A (p.Ala372Thr)	DISP2 (A372T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280483	NM_033510.3(DISP2):c.1199C>T (p.Thr400Ile)	DISP2 (T400I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272169	NM_033510.3(DISP2):c.1255G>C (p.Asp419His)	DISP2 (D419H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403614	NM_033510.3(DISP2):c.1334G>A (p.Gly445Asp)	DISP2 (G445D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082597	NM_033510.3(DISP2):c.1363C>T (p.Arg455Trp)	DISP2 (R455W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082598	NM_033510.3(DISP2):c.1364G>A (p.Arg455Gln)	DISP2 (R455Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531185	NM_033510.3(DISP2):c.1366C>A (p.Leu456Met)	DISP2 (L456M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2645170	NM_033510.3(DISP2):c.1370C>T (p.Ala457Val)	DISP2 (A457V)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2541007	NM_033510.3(DISP2):c.1416G>T (p.Met472Ile)	DISP2 (M472I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473427	NM_033510.3(DISP2):c.1430A>G (p.Lys477Arg)	DISP2 (K477R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082599	NM_033510.3(DISP2):c.1493C>T (p.Ala498Val)	DISP2 (A498V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272176	NM_033510.3(DISP2):c.1594C>G (p.Gln532Glu)	DISP2 (Q532E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272165	NM_033510.3(DISP2):c.1606C>T (p.Arg536Cys)	DISP2 (R536C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295689	NM_033510.3(DISP2):c.1631A>G (p.Asn544Ser)	DISP2 (N544S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082600	NM_033510.3(DISP2):c.1690G>C (p.Asp564His)	DISP2 (D564H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302130	NM_033510.3(DISP2):c.1721C>T (p.Pro574Leu)	DISP2 (P574L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082601	NM_033510.3(DISP2):c.1726G>C (p.Gly576Arg)	DISP2 (G576R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461439	NM_033510.3(DISP2):c.1727G>C (p.Gly576Ala)	DISP2 (G576A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272173	NM_033510.3(DISP2):c.1810T>G (p.Phe604Val)	DISP2 (F604V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272174	NM_033510.3(DISP2):c.1811T>C (p.Phe604Ser)	DISP2 (F604S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082603	NM_033510.3(DISP2):c.1826T>G (p.Leu609Arg)	DISP2 (L609R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597431	NM_033510.3(DISP2):c.1855G>A (p.Ala619Thr)	DISP2 (A619T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399571	NM_033510.3(DISP2):c.1871C>T (p.Thr624Met)	DISP2 (T624M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305383	NM_033510.3(DISP2):c.1930C>A (p.His644Asn)	DISP2 (H644N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272168	NM_033510.3(DISP2):c.1951G>A (p.Gly651Ser)	DISP2 (G651S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363817	NM_033510.3(DISP2):c.1969C>T (p.Arg657Trp)	DISP2 (R657W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082604	NM_033510.3(DISP2):c.1987A>G (p.Ser663Gly)	DISP2 (S663G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486497	NM_033510.3(DISP2):c.1990G>C (p.Ala664Pro)	DISP2 (A664P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082605	NM_033510.3(DISP2):c.2089T>C (p.Cys697Arg)	DISP2 (C697R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316732	NM_033510.3(DISP2):c.2192C>T (p.Thr731Met)	DISP2, LOC130056842 (T731M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592458	NM_033510.3(DISP2):c.2209G>A (p.Gly737Ser)	DISP2, LOC130056842 (G737S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233342	NM_033510.3(DISP2):c.2215G>A (p.Val739Ile)	DISP2, LOC130056842 (V739I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082608	NM_033510.3(DISP2):c.2222G>C (p.Arg741Pro)	DISP2, LOC130056842 (R741P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559071	NM_033510.3(DISP2):c.2251G>T (p.Ala751Ser)	DISP2, LOC130056842 (A751S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279294	NM_033510.3(DISP2):c.2255A>C (p.Glu752Ala)	DISP2, LOC130056842 (E752A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279200	NM_033510.3(DISP2):c.2456C>T (p.Ala819Val)	DISP2 (A819V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397132	NM_033510.3(DISP2):c.2458C>G (p.Arg820Gly)	DISP2 (R820G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409750	NM_033510.3(DISP2):c.2494T>A (p.Trp832Arg)	DISP2 (W832R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599523	NM_033510.3(DISP2):c.2511C>G (p.Phe837Leu)	DISP2 (F837L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082609	NM_033510.3(DISP2):c.2527C>T (p.Arg843Cys)	DISP2 (R843C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315406	NM_033510.3(DISP2):c.2540G>C (p.Ser847Thr)	DISP2 (S847T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392433	NM_033510.3(DISP2):c.2578G>A (p.Gly860Ser)	DISP2 (G860S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296166	NM_033510.3(DISP2):c.2680T>G (p.Phe894Val)	DISP2 (F894V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530426	NM_033510.3(DISP2):c.2696G>A (p.Ser899Asn)	DISP2 (S899N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2310341	NM_033510.3(DISP2):c.2753A>T (p.Asn918Ile)	DISP2 (N918I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272177	NM_033510.3(DISP2):c.2778G>C (p.Glu926Asp)	DISP2 (E926D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272166	NM_033510.3(DISP2):c.2849G>A (p.Arg950His)	DISP2 (R950H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2292179	NM_033510.3(DISP2):c.2950T>C (p.Trp984Arg)	DISP2 (W984R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558124	NM_033510.3(DISP2):c.2952G>C (p.Trp984Cys)	DISP2 (W984C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486267	NM_033510.3(DISP2):c.3053A>G (p.Glu1018Gly)	DISP2 (E1018G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220372	NM_033510.3(DISP2):c.3122A>G (p.His1041Arg)	DISP2 (H1041R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082614	NM_033510.3(DISP2):c.3157G>A (p.Ala1053Thr)	DISP2 (A1053T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597040	NM_033510.3(DISP2):c.3254A>G (p.Tyr1085Cys)	DISP2 (Y1085C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082615	NM_033510.3(DISP2):c.3282G>A (p.Met1094Ile)	DISP2 (M1094I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364329	NM_033510.3(DISP2):c.3410G>C (p.Gly1137Ala)	DISP2 (G1137A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082616	NM_033510.3(DISP2):c.3458G>A (p.Gly1153Glu)	DISP2 (G1153E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272170	NM_033510.3(DISP2):c.3469G>A (p.Gly1157Arg)	DISP2 (G1157R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340444	NM_033510.3(DISP2):c.3481G>A (p.Glu1161Lys)	DISP2 (E1161K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364295	NM_033510.3(DISP2):c.3508C>T (p.Arg1170Trp)	DISP2 (R1170W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240654	NM_033510.3(DISP2):c.3509G>A (p.Arg1170Gln)	DISP2 (R1170Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550857	NM_033510.3(DISP2):c.3511C>T (p.Arg1171Cys)	DISP2 (R1171C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357847	NM_033510.3(DISP2):c.3515G>A (p.Arg1172Gln)	DISP2 (R1172Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082617	NM_033510.3(DISP2):c.3605C>T (p.Pro1202Leu)	DISP2 (P1202L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214432	NM_033510.3(DISP2):c.3611G>A (p.Cys1204Tyr)	DISP2 (C1204Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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