KIF4B[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3114940	NM_001099293.3(KIF4B):c.53C>T (p.Pro18Leu)	KIF4B (P18L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238703	NM_001099293.3(KIF4B):c.224G>T (p.Gly75Val)	KIF4B (G75V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114934	NM_001099293.3(KIF4B):c.257C>A (p.Ala86Asp)	KIF4B (A86D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288640	NM_001099293.3(KIF4B):c.377T>C (p.Ile126Thr)	KIF4B (I126T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609451	NM_001099293.3(KIF4B):c.470A>G (p.Glu157Gly)	KIF4B (E157G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288635	NM_001099293.3(KIF4B):c.475G>C (p.Ala159Pro)	KIF4B (A159P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2629941	NM_001099293.3(KIF4B):c.545T>C (p.Leu182Ser)	KIF4B (L182S)	Single nucleotide variant (missense variant)	KIF4B-related disorder	GUncertain significance
Select item 3044578	NM_001099293.3(KIF4B):c.598G>A (p.Val200Met)	KIF4B (V200M)	Single nucleotide variant (missense variant)	KIF4B-related disorder	GBenign
Select item 2209464	NM_001099293.3(KIF4B):c.607A>G (p.Thr203Ala)	KIF4B (T203A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271295	NM_001099293.3(KIF4B):c.632G>A (p.Arg211Gln)	KIF4B (R211Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3053473	NM_001099293.3(KIF4B):c.658A>G (p.Ile220Val)	KIF4B (I220V)	Single nucleotide variant (missense variant)	KIF4B-related disorder	GBenign
Select item 3114941	NM_001099293.3(KIF4B):c.697C>T (p.Arg233Cys)	KIF4B (R233C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279256	NM_001099293.3(KIF4B):c.716T>C (p.Val239Ala)	KIF4B (V239A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114942	NM_001099293.3(KIF4B):c.761G>A (p.Gly254Glu)	KIF4B (G254E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114943	NM_001099293.3(KIF4B):c.767G>C (p.Arg256Pro)	KIF4B (R256P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618779	NM_001099293.3(KIF4B):c.845A>G (p.Lys282Arg)	KIF4B (K282R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311956	NM_001099293.3(KIF4B):c.901C>G (p.Leu301Val)	KIF4B (L301V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478368	NM_001099293.3(KIF4B):c.932C>A (p.Ala311Asp)	KIF4B (A311D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2565098	NM_001099293.3(KIF4B):c.982C>T (p.Arg328Cys)	KIF4B (R328C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114944	NM_001099293.3(KIF4B):c.983G>A (p.Arg328His)	KIF4B (R328H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114924	NM_001099293.3(KIF4B):c.1007T>C (p.Ile336Thr)	KIF4B (I336T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3050221	NM_001099293.3(KIF4B):c.1152T>C (p.Asn384=)	KIF4B	Single nucleotide variant (synonymous variant)	KIF4B-related disorder	GLikely benign
Select item 3059859	NM_001099293.3(KIF4B):c.1158A>G (p.Gln386=)	KIF4B	Single nucleotide variant (synonymous variant)	KIF4B-related disorder	GBenign
Select item 3288638	NM_001099293.3(KIF4B):c.1184T>C (p.Leu395Pro)	KIF4B (L395P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114925	NM_001099293.3(KIF4B):c.1294G>A (p.Ala432Thr)	KIF4B (A432T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114926	NM_001099293.3(KIF4B):c.1369C>A (p.Gln457Lys)	KIF4B (Q457K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114927	NM_001099293.3(KIF4B):c.1376T>C (p.Leu459Ser)	KIF4B (L459S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387132	NM_001099293.3(KIF4B):c.1381G>A (p.Glu461Lys)	KIF4B (E461K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 791422	NM_001099293.3(KIF4B):c.1393A>T (p.Ile465Leu)	KIF4B (I465L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2283178	NM_001099293.3(KIF4B):c.1404C>A (p.Asn468Lys)	KIF4B (N468K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540752	NM_001099293.3(KIF4B):c.1433A>G (p.Asp478Gly)	KIF4B (D478G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279204	NM_001099293.3(KIF4B):c.1451C>T (p.Thr484Met)	KIF4B (T484M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2208135	NM_001099293.3(KIF4B):c.1465G>A (p.Asp489Asn)	KIF4B (D489N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 783450	NM_001099293.3(KIF4B):c.1480G>C (p.Glu494Gln)	KIF4B (E494Q)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3032081	NM_001099293.3(KIF4B):c.1494G>A (p.Val498=)	KIF4B	Single nucleotide variant (synonymous variant)	KIF4B-related disorder	GLikely benign
Select item 3041807	NM_001099293.3(KIF4B):c.1534A>G (p.Thr512Ala)	KIF4B (T512A)	Single nucleotide variant (missense variant)	KIF4B-related disorder	GLikely benign
Select item 2290554	NM_001099293.3(KIF4B):c.1559C>T (p.Ala520Val)	KIF4B (A520V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3053283	NM_001099293.3(KIF4B):c.1566G>A (p.Met522Ile)	KIF4B (M522I)	Single nucleotide variant (missense variant)	KIF4B-related disorder	GBenign
Select item 2655982	NM_001099293.3(KIF4B):c.1593C>T (p.Asn531=)	KIF4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 710797	NM_001099293.3(KIF4B):c.1638C>T (p.Asn546=)	KIF4B	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3114928	NM_001099293.3(KIF4B):c.1679A>G (p.Asn560Ser)	KIF4B (N560S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315205	NM_001099293.3(KIF4B):c.1687A>C (p.Asn563His)	KIF4B (N563H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2655983	NM_001099293.3(KIF4B):c.1704C>T (p.Val568=)	KIF4B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2569797	NM_001099293.3(KIF4B):c.1769A>G (p.Asn590Ser)	KIF4B (N590S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251447	NM_001099293.3(KIF4B):c.1790A>C (p.His597Pro)	KIF4B (H597P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114929	NM_001099293.3(KIF4B):c.1819G>C (p.Gly607Arg)	KIF4B (G607R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221393	NM_001099293.3(KIF4B):c.1841A>G (p.Lys614Arg)	KIF4B (K614R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480821	NM_001099293.3(KIF4B):c.1859C>T (p.Ser620Phe)	KIF4B (S620F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114930	NM_001099293.3(KIF4B):c.1883C>T (p.Ser628Phe)	KIF4B (S628F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288637	NM_001099293.3(KIF4B):c.1892G>C (p.Arg631Pro)	KIF4B (R631P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570399	NM_001099293.3(KIF4B):c.1892G>A (p.Arg631His)	KIF4B (R631H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114931	NM_001099293.3(KIF4B):c.1912C>A (p.Gln638Lys)	KIF4B (Q638K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297185	NM_001099293.3(KIF4B):c.1954C>T (p.Arg652Cys)	KIF4B (R652C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247633	NM_001099293.3(KIF4B):c.1955G>A (p.Arg652His)	KIF4B (R652H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522596	NM_001099293.3(KIF4B):c.1976A>C (p.Glu659Ala)	KIF4B (E659A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552743	NM_001099293.3(KIF4B):c.1997A>G (p.Gln666Arg)	KIF4B (Q666R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290232	NM_001099293.3(KIF4B):c.2018T>A (p.Ile673Lys)	KIF4B (I673K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3056935	NM_001099293.3(KIF4B):c.2039G>A (p.Arg680His)	KIF4B (R680H)	Single nucleotide variant (missense variant)	KIF4B-related disorder	GBenign
Select item 3114932	NM_001099293.3(KIF4B):c.2076C>G (p.Asn692Lys)	KIF4B (N692K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509215	NM_001099293.3(KIF4B):c.2225G>A (p.Arg742Gln)	KIF4B (R742Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3055323	NM_001099293.3(KIF4B):c.2263G>A (p.Val755Ile)	KIF4B (V755I)	Single nucleotide variant (missense variant)	KIF4B-related disorder	GBenign
Select item 3053843	NM_001099293.3(KIF4B):c.2270C>T (p.Thr757Ile)	KIF4B (T757I)	Single nucleotide variant (missense variant)	KIF4B-related disorder	GBenign
Select item 2218148	NM_001099293.3(KIF4B):c.2321T>G (p.Leu774Arg)	KIF4B (L774R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362509	NM_001099293.3(KIF4B):c.2395A>G (p.Thr799Ala)	KIF4B (T799A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288641	NM_001099293.3(KIF4B):c.2444G>C (p.Cys815Ser)	KIF4B (C815S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3037759	NM_001099293.3(KIF4B):c.2446A>C (p.Ile816Leu)	KIF4B (I816L)	Single nucleotide variant (missense variant)	KIF4B-related disorder	GBenign
Select item 3114933	NM_001099293.3(KIF4B):c.2450C>T (p.Thr817Ile)	KIF4B (T817I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288642	NM_001099293.3(KIF4B):c.2485C>T (p.Leu829Phe)	KIF4B (L829F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555400	NM_001099293.3(KIF4B):c.2543A>C (p.Asp848Ala)	KIF4B (D848A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2655984	NM_001099293.3(KIF4B):c.2551A>G (p.Lys851Glu)	KIF4B (K851E)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3288643	NM_001099293.3(KIF4B):c.2557T>C (p.Cys853Arg)	KIF4B (C853R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288639	NM_001099293.3(KIF4B):c.2582T>C (p.Leu861Pro)	KIF4B (L861P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114935	NM_001099293.3(KIF4B):c.2612T>C (p.Ile871Thr)	KIF4B (I871T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526363	NM_001099293.3(KIF4B):c.2630C>G (p.Ser877Cys)	KIF4B (S877C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242295	NM_001099293.3(KIF4B):c.2638C>T (p.His880Tyr)	KIF4B (H880Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405759	NM_001099293.3(KIF4B):c.2677G>C (p.Ala893Pro)	KIF4B (A893P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3045341	NM_001099293.3(KIF4B):c.2875C>T (p.Leu959=)	KIF4B	Single nucleotide variant (synonymous variant)	KIF4B-related disorder	GLikely benign
Select item 714284	NM_001099293.3(KIF4B):c.2876T>C (p.Leu959Pro)	KIF4B (L959P)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3288644	NM_001099293.3(KIF4B):c.2954A>G (p.Gln985Arg)	KIF4B (Q985R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288645	NM_001099293.3(KIF4B):c.2984T>C (p.Ile995Thr)	KIF4B (I995T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3288646	NM_001099293.3(KIF4B):c.3024T>G (p.Asn1008Lys)	KIF4B (N1008K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548635	NM_001099293.3(KIF4B):c.3031C>T (p.Leu1011Phe)	KIF4B (L1011F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288647	NM_001099293.3(KIF4B):c.3061A>G (p.Ile1021Val)	KIF4B (I1021V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3056311	NM_001099293.3(KIF4B):c.3086G>A (p.Arg1029His)	KIF4B (R1029H)	Single nucleotide variant (missense variant)	KIF4B-related disorder	GBenign
Select item 2411339	NM_001099293.3(KIF4B):c.3165T>G (p.His1055Gln)	KIF4B (H1055Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114937	NM_001099293.3(KIF4B):c.3206A>T (p.Asp1069Val)	KIF4B (D1069V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294626	NM_001099293.3(KIF4B):c.3241T>A (p.Ser1081Thr)	KIF4B (S1081T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288636	NM_001099293.3(KIF4B):c.3255C>G (p.Ile1085Met)	KIF4B (I1085M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457623	NM_001099293.3(KIF4B):c.3325G>T (p.Gly1109Cys)	KIF4B (G1109C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288648	NM_001099293.3(KIF4B):c.3337A>T (p.Ser1113Cys)	KIF4B (S1113C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3049472	NM_001099293.3(KIF4B):c.3357T>C (p.Cys1119=)	KIF4B	Single nucleotide variant (synonymous variant)	KIF4B-related disorder	GLikely benign
Select item 3288649	NM_001099293.3(KIF4B):c.3401A>G (p.Gln1134Arg)	KIF4B (Q1134R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519737	NM_001099293.3(KIF4B):c.3403A>T (p.Thr1135Ser)	KIF4B (T1135S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114938	NM_001099293.3(KIF4B):c.3445G>A (p.Glu1149Lys)	KIF4B (E1149K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598919	NM_001099293.3(KIF4B):c.3452C>T (p.Thr1151Ile)	KIF4B (T1151I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216739	NM_001099293.3(KIF4B):c.3475C>T (p.Pro1159Ser)	KIF4B (P1159S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544593	NM_001099293.3(KIF4B):c.3566C>T (p.Pro1189Leu)	KIF4B (P1189L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209890	NM_001099293.3(KIF4B):c.3589C>T (p.His1197Tyr)	KIF4B (H1197Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3034496	NM_001099293.3(KIF4B):c.3687C>T (p.Ile1229=)	KIF4B	Single nucleotide variant (synonymous variant)	KIF4B-related disorder	GBenign
Select item 3114939	NM_001099293.3(KIF4B):c.3688G>A (p.Glu1230Lys)	KIF4B (E1230K)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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