ClinVar for Gene (Select 9493) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3288538	NM_001367805.3(KIF23):c.786A>T (p.Gln262His)	KIF23 (Q248H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3288537	NM_001367805.3(KIF23):c.1934G>A (p.Arg645His)	KIF23 (R631H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3288536	NM_001367805.3(KIF23):c.1139C>T (p.Thr380Met)	KIF23 (T380M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3288535	NM_001367805.3(KIF23):c.2619G>C (p.Met873Ile)	KIF23 (M755I +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3114685	NM_001367805.3(KIF23):c.89G>T (p.Cys30Phe)	KIF23 (C30F)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3114684	NM_001367805.3(KIF23):c.810G>T (p.Lys270Asn)	KIF23 (K256N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3114683	NM_001367805.3(KIF23):c.2759G>A (p.Ser920Asn)	KIF23 (S906N +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3114681	NM_001367805.3(KIF23):c.2722G>A (p.Asp908Asn)	KIF23 (D894N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3114680	NM_001367805.3(KIF23):c.266T>G (p.Phe89Cys)	KIF23 (F89C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3114679	NM_001367805.3(KIF23):c.2257C>G (p.Pro753Ala)	KIF23 (P739A +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3114678	NM_001367805.3(KIF23):c.1900G>A (p.Glu634Lys)	KIF23 (E510K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3114677	NM_001367805.3(KIF23):c.1736A>G (p.Asn579Ser)	KIF23 (N565S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3114676	NM_001367805.3(KIF23):c.1393C>T (p.Pro465Ser)	KIF23 (P451S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3114675	NM_001367805.3(KIF23):c.121G>A (p.Glu41Lys)	KIF23 (E41K)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3064722	NM_001367805.3(KIF23):c.1324A>G (p.Arg442Gly)	KIF23 (R318G +2 more)	Single nucleotide variant (missense variant +1 more)	Congenital dyserythropoietic anemia, type III	GUncertain significance
Select item 3057853	NM_001367805.3(KIF23):c.2307A>G (p.Gln769=)	KIF23	Single nucleotide variant (synonymous variant +2 more)	KIF23-related disorder	GLikely benign
Select item 3056833	NM_001367805.3(KIF23):c.2110-10A>C	KIF23	Single nucleotide variant (intron variant)	KIF23-related disorder	GLikely benign
Select item 3054710	NM_001367805.3(KIF23):c.168T>C (p.Thr56=)	KIF23	Single nucleotide variant (5 prime UTR variant +2 more)	KIF23-related disorder	GLikely benign
Select item 3048864	NM_001367805.3(KIF23):c.1323G>A (p.Met441Ile)	KIF23 (M317I +2 more)	Single nucleotide variant (missense variant +1 more)	KIF23-related disorder	GUncertain significance
Select item 3023192	NM_001367805.3(KIF23):c.777-14T>C	KIF23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3009039	NM_001367805.3(KIF23):c.551C>G (p.Thr184Ser)	KIF23 (T74S +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3004325	NM_001367805.3(KIF23):c.563+12T>C	KIF23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3002458	NM_001367805.3(KIF23):c.357T>G (p.Thr119=)	KIF23	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 3001496	NM_001367805.3(KIF23):c.1469G>A (p.Ser490Asn)	KIF23 (S476N +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2999821	NM_001367805.3(KIF23):c.2461C>T (p.Leu821Phe)	KIF23 (L703F +2 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2999296	NM_001367805.3(KIF23):c.379G>A (p.Gly127Arg)	KIF23 (G127R)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2990048	NM_001367805.3(KIF23):c.211-17_211-13del	KIF23	Deletion (intron variant)	not provided	GLikely benign
Select item 2979060	NM_001367805.3(KIF23):c.453+18G>C	KIF23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2974983	NM_001367805.3(KIF23):c.1511A>G (p.Asp504Gly)	KIF23 (D380G +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2973806	NM_001367805.3(KIF23):c.929G>A (p.Arg310His)	KIF23 (R186H +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2973412	NM_001367805.3(KIF23):c.2631G>A (p.Gln877=)	KIF23	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2973171	NM_001367805.3(KIF23):c.57A>G (p.Gln19=)	KIF23	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GLikely benign
Select item 2971340	NM_001367805.3(KIF23):c.1713A>G (p.Glu571=)	KIF23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2971235	NM_001367805.3(KIF23):c.971T>C (p.Val324Ala)	KIF23 (V310A +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2968735	NM_001367805.3(KIF23):c.621A>C (p.Ala207=)	KIF23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2968572	NM_001367805.3(KIF23):c.1930-3T>C	KIF23	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2968445	NM_001367805.3(KIF23):c.2674-18C>G	KIF23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2967288	NM_001367805.3(KIF23):c.1397G>A (p.Gly466Glu)	KIF23 (G342E +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2967115	NM_001367805.3(KIF23):c.2304A>G (p.Gly768=)	KIF23	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2966300	NM_001367805.3(KIF23):c.861T>C (p.Thr287=)	KIF23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2965518	NM_001367805.3(KIF23):c.1011+15T>C	KIF23	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 2962449	NM_001367805.3(KIF23):c.12-3_12-2dup	KIF23	Duplication (splice acceptor variant)	not provided	GUncertain significance
Select item 2961575	NM_001367805.3(KIF23):c.1317A>G (p.Gln439=)	KIF23	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 2918503	NM_001367805.3(KIF23):c.84A>G (p.Val28=)	KIF23	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GBenign
Select item 2914617	NM_001367805.3(KIF23):c.2143G>A (p.Gly715Ser)	KIF23 (G591S +2 more)	Single nucleotide variant (missense variant +2 more)	not provided	GConflicting classifications of pathogenicity
Select item 2910800	NM_001367805.3(KIF23):c.2871C>G (p.Ser957=)	KIF23	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2909426	NM_001367805.3(KIF23):c.553TCT[1] (p.Ser187del)	KIF23 (S77del +1 more)	Microsatellite (inframe_deletion +1 more)	not provided	GUncertain significance
Select item 2903713	NM_001367805.3(KIF23):c.454-10C>T	KIF23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2897898	NM_001367805.3(KIF23):c.1484_1485inv (p.Pro495Leu)	KIF23 (P371L +2 more)	Inversion (missense variant +1 more)	not provided	GUncertain significance
Select item 2894770	NM_001367805.3(KIF23):c.2223G>A (p.Ser741=)	KIF23	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2894688	NM_001367805.3(KIF23):c.731C>G (p.Pro244Arg)	KIF23 (P134R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2891419	NM_001367805.3(KIF23):c.1034G>C (p.Ser345Thr)	KIF23 (S221T +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2890902	NM_001367805.3(KIF23):c.2175T>C (p.His725=)	KIF23	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2889742	NM_001367805.3(KIF23):c.1929+10G>A	KIF23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2889062	NM_001367805.3(KIF23):c.636A>G (p.Glu212=)	KIF23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2885518	NM_001367805.3(KIF23):c.2514C>T (p.Pro838=)	KIF23	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 2881207	NM_001367805.3(KIF23):c.2190T>G (p.Ser730=)	KIF23	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2880974	NM_001367805.3(KIF23):c.835T>A (p.Cys279Ser)	KIF23 (C265S +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2868586	NM_001367805.3(KIF23):c.2123A>G (p.Tyr708Cys)	KIF23 (Y584C +2 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2861784	NM_001367805.3(KIF23):c.2143_2144delinsTT (p.Gly715Phe)	KIF23 (G715F +2 more)	Indel (missense variant +2 more)	not provided	GUncertain significance
Select item 2835718	NM_001367805.3(KIF23):c.2079T>C (p.Thr693=)	KIF23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2834647	NM_001367805.3(KIF23):c.11+17C>G	KIF23, KIF23-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2817334	NM_001367805.3(KIF23):c.63C>A (p.Asn21Lys)	KIF23 (N21K)	Single nucleotide variant (5 prime UTR variant +2 more)	not provided	GUncertain significance
Select item 2815217	NM_001367805.3(KIF23):c.1115-4T>G	KIF23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2809024	NM_001367805.3(KIF23):c.2367G>T (p.Glu789Asp)	KIF23 (E665D +2 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2794277	NM_001367805.3(KIF23):c.2449CCA[1] (p.Pro818del)	KIF23 (P804del +2 more)	Microsatellite (inframe_deletion +2 more)	not provided	GUncertain significance
Select item 2790085	NM_001367805.3(KIF23):c.2295G>A (p.Gln765=)	KIF23	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2788179	NM_001367805.3(KIF23):c.1438+15T>C	KIF23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2781751	NM_001367805.3(KIF23):c.1527A>G (p.Pro509=)	KIF23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2761568	NM_001367805.3(KIF23):c.2355T>C (p.Thr785=)	KIF23	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2755136	NM_001367805.3(KIF23):c.1779T>C (p.Thr593=)	KIF23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2746272	NM_001367805.3(KIF23):c.798T>A (p.Leu266=)	KIF23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2745537	NM_001367805.3(KIF23):c.1008A>G (p.Leu336=)	KIF23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2726450	NM_001367805.3(KIF23):c.2142C>A (p.Asn714Lys)	KIF23 (N700K +2 more)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 2726105	NM_001367805.3(KIF23):c.1176A>G (p.Gln392=)	KIF23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2722713	NM_001367805.3(KIF23):c.563+6del	KIF23	Deletion (intron variant)	not provided	GUncertain significance
Select item 2721463	NM_001367805.3(KIF23):c.2465G>A (p.Arg822Gln)	KIF23 (R704Q +2 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2715727	NM_001367805.3(KIF23):c.975G>A (p.Gln325=)	KIF23	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2715463	NM_001367805.3(KIF23):c.2756+13C>A	KIF23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2715210	NM_001367805.3(KIF23):c.2315C>T (p.Thr772Ile)	KIF23 (T758I +2 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2702690	NM_001367805.3(KIF23):c.777A>G (p.Val259=)	KIF23	Single nucleotide variant (synonymous variant +1 more)	not provided	GUncertain significance
Select item 2697792	NM_001367805.3(KIF23):c.210+15G>A	KIF23	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2689313	NM_001367805.3(KIF23):c.2479C>T (p.Arg827Cys)	KIF23 (R709C +2 more)	Single nucleotide variant (missense variant +2 more)	Congenital dyserythropoietic anemia, type III	GUncertain significance
Select item 2689312	NM_001367805.3(KIF23):c.999C>A (p.Asp333Glu)	KIF23 (D209E +2 more)	Single nucleotide variant (missense variant +1 more)	Congenital dyserythropoietic anemia, type III	GUncertain significance
Select item 2689311	NM_001367805.3(KIF23):c.844G>A (p.Val282Ile)	KIF23 (V158I +2 more)	Single nucleotide variant (missense variant +1 more)	Congenital dyserythropoietic anemia, type III	GUncertain significance
Select item 2689310	NM_001367805.3(KIF23):c.2089G>C (p.Val697Leu)	KIF23 (V573L +2 more)	Single nucleotide variant (missense variant +1 more)	Congenital dyserythropoietic anemia, type III	GUncertain significance
Select item 2683321	NM_001367805.3(KIF23):c.2696G>C (p.Gly899Ala)	KIF23 (G691A +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2683320	NM_001367805.3(KIF23):c.1978G>A (p.Val660Ile)	KIF23 (V536I +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2683319	NM_001367805.3(KIF23):c.500T>C (p.Val167Ala)	KIF23 (V167A +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2645495	NM_001367805.3(KIF23):c.1489T>C (p.Cys497Arg)	KIF23 (C373R +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 2645494	NM_001367805.3(KIF23):c.1119T>C (p.Asn373=)	KIF23	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2636408	NM_001367805.3(KIF23):c.2762G>A (p.Arg921Gln)	KIF23 (R713Q +3 more)	Single nucleotide variant (missense variant +2 more)	KIF23-related disorder +1 more	GUncertain significance
Select item 2597070	NM_001367805.3(KIF23):c.1508A>G (p.Asn503Ser)	KIF23 (N379S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2591934	NM_001367805.3(KIF23):c.1904C>T (p.Thr635Met)	KIF23 (T635M +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2582639	NM_001367805.3(KIF23):c.2482T>A (p.Ser828Thr)	KIF23 (S710T +2 more)	Single nucleotide variant (missense variant +2 more)	Congenital dyserythropoietic anemia, type III	GUncertain significance
Select item 2555497	NM_001367805.3(KIF23):c.1323G>C (p.Met441Ile)	KIF23 (M317I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550451	NM_001367805.3(KIF23):c.1553G>A (p.Arg518Gln)	KIF23 (R504Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2531728	NM_001367805.3(KIF23):c.1556A>G (p.His519Arg)	KIF23 (H395R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2531727	NM_001367805.3(KIF23):c.1541C>T (p.Ala514Val)	KIF23 (A500V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2515808	NM_001367805.3(KIF23):c.517C>T (p.Arg173Cys)	KIF23 (R63C +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance

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