ClinVar for Gene (Select 9909) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3351462	NM_014856.3(DENND4B):c.4115-3C>T	DENND4B	Single nucleotide variant (intron variant)	DENND4B-related disorder	GLikely benign
Select item 3346216	NM_014856.3(DENND4B):c.361G>A (p.Val121Met)	DENND4B (V121M +1 more)	Single nucleotide variant (missense variant)	DENND4B-related disorder	GUncertain significance
Select item 3271577	NM_014856.3(DENND4B):c.2816G>A (p.Arg939His)	DENND4B (R950H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271576	NM_014856.3(DENND4B):c.29T>C (p.Val10Ala)	DENND4B (V10A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271575	NM_014856.3(DENND4B):c.2866G>A (p.Gly956Arg)	DENND4B (G967R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271574	NM_014856.3(DENND4B):c.1787C>T (p.Ala596Val)	DENND4B (A596V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271573	NM_014856.3(DENND4B):c.4097T>C (p.Val1366Ala)	DENND4B (V1366A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271572	NM_014856.3(DENND4B):c.40G>A (p.Val14Met)	DENND4B (V25M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271570	NM_014856.3(DENND4B):c.1285C>T (p.Arg429Trp)	DENND4B (R429W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271569	NM_014856.3(DENND4B):c.1972C>A (p.Pro658Thr)	DENND4B (P669T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271568	NM_014856.3(DENND4B):c.3847G>A (p.Glu1283Lys)	DENND4B (E1294K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3247808	NC_000001.10:g.(?_153782653)_(154580482_?)dup	ADAR, AQP10 +20 more	Duplication	Symmetrical dyschromatosis of extremities +1 more	GUncertain significance
Select item 3081623	NM_014856.3(DENND4B):c.823G>A (p.Ala275Thr)	DENND4B (A286T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081622	NM_014856.3(DENND4B):c.697G>A (p.Val233Met)	DENND4B (V244M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081621	NM_014856.3(DENND4B):c.623C>T (p.Thr208Met)	DENND4B (T208M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081620	NM_014856.3(DENND4B):c.556C>T (p.Leu186Phe)	DENND4B (L197F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081619	NM_014856.3(DENND4B):c.551G>A (p.Arg184His)	DENND4B (R184H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081618	NM_014856.3(DENND4B):c.3647G>T (p.Gly1216Val)	DENND4B (G1216V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081617	NM_014856.3(DENND4B):c.3438G>C (p.Gln1146His)	DENND4B (Q1146H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081616	NM_014856.3(DENND4B):c.340C>T (p.Arg114Cys)	DENND4B (R125C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081614	NM_014856.3(DENND4B):c.3301C>T (p.Arg1101Trp)	DENND4B (R1101W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081612	NM_014856.3(DENND4B):c.2911C>A (p.Gln971Lys)	DENND4B (Q982K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081611	NM_014856.3(DENND4B):c.2765C>T (p.Ser922Phe)	DENND4B (S933F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081609	NM_014856.3(DENND4B):c.2618G>A (p.Arg873His)	DENND4B (R873H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081608	NM_014856.3(DENND4B):c.2611C>T (p.Arg871Cys)	DENND4B (R871C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081607	NM_014856.3(DENND4B):c.2576T>G (p.Leu859Trp)	DENND4B (L859W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081606	NM_014856.3(DENND4B):c.233A>T (p.Glu78Val)	DENND4B (E78V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081605	NM_014856.3(DENND4B):c.1996A>G (p.Thr666Ala)	DENND4B (T666A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081603	NM_014856.3(DENND4B):c.1859A>G (p.Tyr620Cys)	DENND4B (Y620C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081602	NM_014856.3(DENND4B):c.173G>C (p.Gly58Ala)	DENND4B (G58A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081601	NM_014856.3(DENND4B):c.1715G>A (p.Arg572His)	DENND4B (R583H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081600	NM_014856.3(DENND4B):c.1276C>T (p.His426Tyr)	DENND4B (H437Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081599	NM_014856.3(DENND4B):c.115C>T (p.Arg39Cys)	DENND4B (R39C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3081598	NM_014856.3(DENND4B):c.1139A>G (p.Asn380Ser)	DENND4B (N391S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063532	GRCh37/hg19 1q21.1-23.1(chr1:146577511-157155587)x3	ACP6, ADAM15 +263 more	Copy number gain	not specified	GPathogenic
Select item 3062988	GRCh37/hg19 1q21.1-23.1(chr1:144368497-158992086)x3	ACP6, ADAM15 +315 more	Copy number gain	not specified	GPathogenic
Select item 3061201	NM_014856.3(DENND4B):c.2704CAG[16] (p.Gln910_Glu911insGlnGlnGlnGlnGlnGlnGln)	DENND4B	Microsatellite	DENND4B-related disorder	GUncertain significance
Select item 3059203	NM_014856.3(DENND4B):c.2704CAG[6] (p.Gln908_Gln910del)	DENND4B	Microsatellite	DENND4B-related disorder	GBenign
Select item 3058049	NM_014856.3(DENND4B):c.1819+4T>C	DENND4B	Single nucleotide variant (intron variant)	DENND4B-related disorder	GLikely benign
Select item 3057373	NM_014856.3(DENND4B):c.690C>T (p.Pro230=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related disorder	GLikely benign
Select item 3056982	NM_014856.3(DENND4B):c.39C>T (p.Phe13=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related disorder	GLikely benign
Select item 3055732	NM_014856.3(DENND4B):c.-6G>C	DENND4B (G10R)	Single nucleotide variant (missense variant +1 more)	DENND4B-related disorder	GBenign
Select item 3053889	NM_014856.3(DENND4B):c.897C>T (p.Ser299=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related disorder	GLikely benign
Select item 3052690	NM_014856.3(DENND4B):c.2103C>T (p.Tyr701=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related disorder	GBenign
Select item 3052285	NM_014856.3(DENND4B):c.3269G>A (p.Arg1090His)	DENND4B (R1090H +1 more)	Single nucleotide variant (missense variant)	DENND4B-related disorder	GLikely benign
Select item 3051405	NM_014856.3(DENND4B):c.4374C>G (p.Ala1458=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related disorder	GLikely benign
Select item 3051109	NM_014856.3(DENND4B):c.1905G>A (p.Glu635=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related disorder	GLikely benign
Select item 3050560	NM_014856.3(DENND4B):c.948T>C (p.Arg316=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related disorder	GLikely benign
Select item 3049934	NM_014856.3(DENND4B):c.703G>A (p.Val235Ile)	DENND4B (V235I +1 more)	Single nucleotide variant (missense variant)	DENND4B-related disorder	GLikely benign
Select item 3048357	NM_014856.3(DENND4B):c.3036G>A (p.Pro1012=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related disorder	GLikely benign
Select item 3048236	NM_014856.3(DENND4B):c.3624-6C>T	DENND4B	Single nucleotide variant (intron variant)	DENND4B-related disorder	GLikely benign
Select item 3046379	NM_014856.3(DENND4B):c.1665G>A (p.Val555=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related disorder	GLikely benign
Select item 3045601	NM_014856.3(DENND4B):c.843G>A (p.Ala281=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related disorder	GBenign
Select item 3044596	NM_014856.3(DENND4B):c.4311A>G (p.Thr1437=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related disorder	GBenign
Select item 3044585	NM_014856.3(DENND4B):c.108G>C (p.Gly36=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related disorder	GBenign
Select item 3043052	NM_014856.3(DENND4B):c.2439+10C>T	DENND4B	Single nucleotide variant (intron variant)	DENND4B-related disorder	GLikely benign
Select item 3042126	NM_014856.3(DENND4B):c.2704CAG[10] (p.Gln910_Glu911insGln)	DENND4B	Microsatellite	DENND4B-related disorder	GLikely benign
Select item 3037524	NM_014856.3(DENND4B):c.2703A>G (p.Gln901=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related disorder	GBenign
Select item 3034631	NM_014856.3(DENND4B):c.4419C>T (p.His1473=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related disorder	GLikely benign
Select item 3033812	NM_014856.3(DENND4B):c.1056-3del	DENND4B	Deletion (intron variant)	DENND4B-related disorder	GLikely benign
Select item 3033743	NM_014856.3(DENND4B):c.3913T>C (p.Leu1305=)	DENND4B	Single nucleotide variant (synonymous variant)	DENND4B-related disorder	GLikely benign
Select item 3033510	NM_014856.3(DENND4B):c.2703_2729del (p.Gln902_Gln910del)	DENND4B	Deletion	DENND4B-related disorder	GLikely benign
Select item 2639364	NM_014856.3(DENND4B):c.30G>A (p.Val10=)	DENND4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2639363	NM_014856.3(DENND4B):c.1317C>G (p.Ala439=)	DENND4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2633376	NM_014856.3(DENND4B):c.1318C>G (p.Leu440Val)	DENND4B (L440V +1 more)	Single nucleotide variant (missense variant)	DENND4B-related disorder	GUncertain significance
Select item 2628853	NM_014856.3(DENND4B):c.46G>A (p.Ala16Thr)	DENND4B (A16T +1 more)	Single nucleotide variant (missense variant)	DENND4B-related disorder	GUncertain significance
Select item 2602567	NM_014856.3(DENND4B):c.3385C>G (p.Leu1129Val)	DENND4B (L1140V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597102	NM_014856.3(DENND4B):c.2929G>A (p.Gly977Ser)	DENND4B (G988S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596808	NM_014856.3(DENND4B):c.3409C>T (p.Arg1137Cys)	DENND4B (R1148C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594055	NM_014856.3(DENND4B):c.1681C>T (p.Arg561Trp)	DENND4B (R561W +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2593533	NM_014856.3(DENND4B):c.3268C>T (p.Arg1090Cys)	DENND4B (R1090C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591016	NM_014856.3(DENND4B):c.307G>A (p.Val103Ile)	DENND4B (V114I +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2580317	GRCh37/hg19 1q12-23.1(chr1:142535935-157648813)x3	ACP6, ADAM15 +293 more	Copy number gain	Chromosome 1q21.1 duplication syndrome	GPathogenic
Select item 2559232	NM_014856.3(DENND4B):c.332G>A (p.Gly111Glu)	DENND4B (G122E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549068	NM_014856.3(DENND4B):c.425G>A (p.Arg142His)	DENND4B (R142H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549030	NM_014856.3(DENND4B):c.3395G>A (p.Arg1132His)	DENND4B (R1132H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546955	NM_014856.3(DENND4B):c.2239A>G (p.Lys747Glu)	DENND4B (K758E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544691	NM_014856.3(DENND4B):c.445C>T (p.Arg149Trp)	DENND4B (R149W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540957	NM_014856.3(DENND4B):c.1631C>G (p.Ser544Cys)	DENND4B (S555C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535384	NM_014856.3(DENND4B):c.448G>A (p.Ala150Thr)	DENND4B (A150T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530121	NM_014856.3(DENND4B):c.2797C>T (p.Pro933Ser)	DENND4B (P933S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525332	NM_014856.3(DENND4B):c.290G>A (p.Arg97His)	DENND4B (R108H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511012	NM_014856.3(DENND4B):c.268G>A (p.Val90Ile)	DENND4B (V101I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489573	NM_014856.3(DENND4B):c.371C>G (p.Thr124Arg)	DENND4B (T135R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482553	NM_014856.3(DENND4B):c.751A>G (p.Thr251Ala)	DENND4B (T262A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476875	NM_014856.3(DENND4B):c.2869C>G (p.Arg957Gly)	DENND4B (R957G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475550	NM_014856.3(DENND4B):c.3250G>A (p.Asp1084Asn)	DENND4B (D1084N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473748	NM_014856.3(DENND4B):c.3617G>A (p.Arg1206Gln)	DENND4B (R1217Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459470	NM_014856.3(DENND4B):c.3266C>T (p.Ala1089Val)	DENND4B (A1100V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458663	NM_014856.3(DENND4B):c.994G>A (p.Ala332Thr)	DENND4B (A332T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456347	NM_014856.3(DENND4B):c.886G>A (p.Gly296Ser)	DENND4B (G307S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2426580	NC_000001.10:g.(?_153782653)_(153964569_?)del	CREB3L4, CRTC2 +6 more	Deletion	not provided	GPathogenic
Select item 2410685	NM_014856.3(DENND4B):c.3289C>A (p.Leu1097Ile)	DENND4B (L1108I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386592	NM_014856.3(DENND4B):c.3115C>T (p.Arg1039Trp)	DENND4B (R1050W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382212	NM_014856.3(DENND4B):c.926G>A (p.Gly309Asp)	DENND4B (G320D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373200	NM_014856.3(DENND4B):c.1040G>A (p.Arg347His)	DENND4B (R358H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371358	NM_014856.3(DENND4B):c.2192G>A (p.Arg731His)	DENND4B (R731H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371083	NM_014856.3(DENND4B):c.371C>T (p.Thr124Met)	DENND4B (T135M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365151	NM_014856.3(DENND4B):c.2532T>G (p.Ile844Met)	DENND4B (I855M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356679	NM_014856.3(DENND4B):c.3419A>T (p.Asp1140Val)	DENND4B (D1140V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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