ClinVar for Gene (Select 23046) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3371811	NM_001252102.2(KIF21B):c.1403-1G>C	KIF21B	Single nucleotide variant (splice acceptor variant)	not provided	GUncertain significance
Select item 3371204	NM_001252102.2(KIF21B):c.901-1G>C	KIF21B	Single nucleotide variant (splice acceptor variant)	not provided	GUncertain significance
Select item 3371162	NM_001252102.2(KIF21B):c.1235A>G (p.Asp412Gly)	KIF21B (D412G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3368913	NM_001252102.2(KIF21B):c.2036G>C (p.Arg679Pro)	KIF21B (R679P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3366005	NM_001252102.2(KIF21B):c.257A>G (p.Tyr86Cys)	KIF21B (Y86C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3365860	NM_001252102.2(KIF21B):c.4006G>A (p.Val1336Ile)	KIF21B, LOC129932203 (V1323I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3365231	NM_001252102.2(KIF21B):c.211C>T (p.Leu71Phe)	KIF21B (L71F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3364246	NM_001252102.2(KIF21B):c.2748del (p.Trp916fs)	KIF21B (W916fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 3362171	NM_001252102.2(KIF21B):c.2853C>A (p.Phe951Leu)	KIF21B (F951L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3361587	NM_001252102.2(KIF21B):c.1609G>C (p.Ala537Pro)	KIF21B (A537P)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3359651	NM_001252102.2(KIF21B):c.2321G>A (p.Arg774Gln)	KIF21B (R774Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3359650	NM_001252102.2(KIF21B):c.2455-3C>T	KIF21B	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3358954	NM_001252102.2(KIF21B):c.1451A>G (p.Glu484Gly)	KIF21B (E484G)	Single nucleotide variant (missense variant)	KIF21B-associated neurodevelopmental disorder	GUncertain significance
Select item 3343305	NM_001252102.2(KIF21B):c.3736C>G (p.Pro1246Ala)	KIF21B (P1246A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3337223	NM_001252102.2(KIF21B):c.631C>T (p.Arg211Cys)	KIF21B (R211C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3288531	NM_001252102.2(KIF21B):c.1303C>T (p.Arg435Trp)	KIF21B (R435W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288530	NM_001252102.2(KIF21B):c.4277T>C (p.Met1426Thr)	KIF21B, LOC126805976 (M1413T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288529	NM_001252102.2(KIF21B):c.569C>A (p.Thr190Asn)	KIF21B (T190N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288528	NM_001252102.2(KIF21B):c.776C>T (p.Ser259Leu)	KIF21B (S259L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288527	NM_001252102.2(KIF21B):c.4547T>G (p.Ile1516Ser)	KIF21B (I1503S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288526	NM_001252102.2(KIF21B):c.1438A>G (p.Asn480Asp)	KIF21B (N480D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288525	NM_001252102.2(KIF21B):c.509G>A (p.Arg170His)	KIF21B (R170H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288524	NM_001252102.2(KIF21B):c.104C>T (p.Pro35Leu)	KIF21B (P35L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288523	NM_001252102.2(KIF21B):c.2506C>T (p.Arg836Cys)	KIF21B (R836C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288522	NM_001252102.2(KIF21B):c.3167G>A (p.Arg1056Gln)	KIF21B (R1056Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3257071	NM_001252102.2(KIF21B):c.216C>T (p.Ile72=)	KIF21B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3254547	NM_001252102.2(KIF21B):c.4670_4671insT (p.Met1559fs)	KIF21B (M1546fs +1 more)	Insertion (frameshift variant)	Neurodevelopmental disorder	GUncertain significance
Select item 3253410	NM_001252102.2(KIF21B):c.3994A>T (p.Met1332Leu)	KIF21B, LOC129932203 (M1319L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3248093	NC_000001.10:g.(?_190829412)_(216061974_?)del	RPS6KC1, SERTAD4 +185 more	Deletion	not provided	GPathogenic
Select item 3114666	NM_001252102.2(KIF21B):c.95C>T (p.Ser32Phe)	KIF21B (S32F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114665	NM_001252102.2(KIF21B):c.864G>C (p.Glu288Asp)	KIF21B (E288D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114664	NM_001252102.2(KIF21B):c.743C>T (p.Ala248Val)	KIF21B (A248V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114663	NM_001252102.2(KIF21B):c.649C>G (p.Gln217Glu)	KIF21B (Q217E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114662	NM_001252102.2(KIF21B):c.5C>A (p.Ala2Asp)	KIF21B (A2D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114661	NM_001252102.2(KIF21B):c.4697C>T (p.Ala1566Val)	KIF21B (A1553V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114660	NM_001252102.2(KIF21B):c.4285G>A (p.Ala1429Thr)	KIF21B, LOC126805976 (A1416T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114659	NM_001252102.2(KIF21B):c.382A>G (p.Lys128Glu)	KIF21B (K128E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114658	NM_001252102.2(KIF21B):c.364G>C (p.Gly122Arg)	KIF21B (G122R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114657	NM_001252102.2(KIF21B):c.3551G>A (p.Arg1184Gln)	KIF21B (R1184Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114656	NM_001252102.2(KIF21B):c.3241C>T (p.Arg1081Cys)	KIF21B (R1081C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114655	NM_001252102.2(KIF21B):c.2881C>G (p.Arg961Gly)	KIF21B (R961G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114654	NM_001252102.2(KIF21B):c.2804A>G (p.Asn935Ser)	KIF21B (N935S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114653	NM_001252102.2(KIF21B):c.2659C>T (p.Pro887Ser)	KIF21B (P887S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114652	NM_001252102.2(KIF21B):c.2528T>C (p.Met843Thr)	KIF21B (M843T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114651	NM_001252102.2(KIF21B):c.2396G>A (p.Arg799Gln)	KIF21B (R799Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114649	NM_001252102.2(KIF21B):c.2345G>A (p.Arg782Gln)	KIF21B (R782Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114648	NM_001252102.2(KIF21B):c.2219G>A (p.Arg740His)	KIF21B (R740H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114647	NM_001252102.2(KIF21B):c.2212C>G (p.Gln738Glu)	KIF21B (Q738E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114646	NM_001252102.2(KIF21B):c.2144G>A (p.Arg715Gln)	KIF21B (R715Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114645	NM_001252102.2(KIF21B):c.1490C>T (p.Ala497Val)	KIF21B (A497V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114644	NM_001252102.2(KIF21B):c.1316A>C (p.Lys439Thr)	KIF21B (K439T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114643	NM_001252102.2(KIF21B):c.1174A>G (p.Ile392Val)	KIF21B (I392V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062955	GRCh37/hg19 1q32.1(chr1:199373229-204335027)x3	ADIPOR1, ADORA1 +58 more	Copy number gain	not specified	GLikely pathogenic
Select item 3062655	GRCh37/hg19 1q31.3-32.1(chr1:197216705-203683110)x1	ADIPOR1, ADORA1 +57 more	Copy number loss	not specified	GLikely pathogenic
Select item 3061811	NM_001252102.2(KIF21B):c.1061T>C (p.Phe354Ser)	KIF21B (F354S)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder	GUncertain significance
Select item 3056207	NM_001252102.2(KIF21B):c.246G>A (p.Thr82=)	KIF21B	Single nucleotide variant (synonymous variant)	KIF21B-related disorder	GBenign
Select item 3041759	NM_001252102.2(KIF21B):c.2507G>A (p.Arg836His)	KIF21B (R836H)	Single nucleotide variant (missense variant)	KIF21B-related disorder	GLikely benign
Select item 3035462	NM_001252102.2(KIF21B):c.4043C>T (p.Pro1348Leu)	KIF21B (P1335L +1 more)	Single nucleotide variant (missense variant)	KIF21B-related disorder	GLikely benign
Select item 2704397	NM_001252102.2(KIF21B):c.3886G>A (p.Ala1296Thr)	KIF21B (A1296T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2663269	NM_001252102.2(KIF21B):c.2992G>A (p.Asp998Asn)	KIF21B (D998N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2639741	NM_001252102.2(KIF21B):c.90T>C (p.Cys30=)	KIF21B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2639740	NM_001252102.2(KIF21B):c.273C>T (p.Ala91=)	KIF21B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2639739	NM_001252102.2(KIF21B):c.957C>T (p.His319=)	KIF21B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2639738	NM_001252102.2(KIF21B):c.1814G>A (p.Arg605His)	KIF21B (R605H)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2639737	NM_001252102.2(KIF21B):c.1816G>A (p.Glu606Lys)	KIF21B (E606K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2639736	NM_001252102.2(KIF21B):c.1836G>C (p.Ser612=)	KIF21B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2639735	NM_001252102.2(KIF21B):c.2145G>A (p.Arg715=)	KIF21B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2639734	NM_001252102.2(KIF21B):c.2216C>T (p.Ser739Leu)	KIF21B (S739L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2639733	NM_001252102.2(KIF21B):c.2223C>T (p.Tyr741=)	KIF21B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2639732	NM_001252102.2(KIF21B):c.3447G>A (p.Ser1149=)	KIF21B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2639731	NM_001252102.2(KIF21B):c.3669C>T (p.Tyr1223=)	KIF21B	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2636861	NM_001252102.2(KIF21B):c.191dup (p.Tyr64Ter)	KIF21B (Y64*)	Duplication (nonsense)	KIF21B-related disorder	GUncertain significance
Select item 2632149	NM_001252102.2(KIF21B):c.197C>G (p.Thr66Ser)	KIF21B (T66S)	Single nucleotide variant (missense variant)	KIF21B-related disorder	GUncertain significance
Select item 2611441	NM_001252102.2(KIF21B):c.1496A>G (p.Asn499Ser)	KIF21B (N499S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611026	NM_001252102.2(KIF21B):c.3565C>G (p.Arg1189Gly)	KIF21B (R1189G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610146	NM_001252102.2(KIF21B):c.1820A>T (p.Asp607Val)	KIF21B (D607V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602210	NM_001252102.2(KIF21B):c.395A>G (p.Gln132Arg)	KIF21B (Q132R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593690	NM_001252102.2(KIF21B):c.3641C>T (p.Thr1214Met)	KIF21B (T1214M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2582103	NM_001252102.2(KIF21B):c.2408C>T (p.Ser803Phe)	KIF21B (S803F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2580006	NM_001252102.2(KIF21B):c.3053C>A (p.Thr1018Lys)	KIF21B (T1018K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2578240	NM_001252102.2(KIF21B):c.1013A>T (p.Asn338Ile)	KIF21B (N338I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2577697	NM_001252102.2(KIF21B):c.4564C>T (p.Arg1522Ter)	KIF21B (R1509* +1 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2577664	NM_001252102.2(KIF21B):c.4521C>G (p.Ile1507Met)	KIF21B (I1494M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2576654	NM_001252102.2(KIF21B):c.1444A>T (p.Ile482Phe)	KIF21B (I482F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2574384	NM_001252102.2(KIF21B):c.127G>A (p.Gly43Arg)	KIF21B (G43R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2574179	NM_001252102.2(KIF21B):c.4615-3C>G	KIF21B	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2572693	NM_001252102.2(KIF21B):c.2079C>A (p.Ser693Arg)	KIF21B (S693R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2558607	NM_001252102.2(KIF21B):c.1781G>C (p.Arg594Pro)	KIF21B (R594P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558011	NM_001252102.2(KIF21B):c.4459G>A (p.Glu1487Lys)	KIF21B (E1487K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555594	NM_001252102.2(KIF21B):c.462G>T (p.Glu154Asp)	KIF21B (E154D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547184	NM_001252102.2(KIF21B):c.4815-546A>G	KIF21B (I1616V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545893	NM_001252102.2(KIF21B):c.3872A>G (p.Lys1291Arg)	KIF21B (K1291R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543409	NM_001252102.2(KIF21B):c.3442G>C (p.Val1148Leu)	KIF21B (V1148L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541207	NM_001252102.2(KIF21B):c.1372C>G (p.Gln458Glu)	KIF21B (Q458E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532886	NM_001252102.2(KIF21B):c.2558G>A (p.Ser853Asn)	KIF21B (S853N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530611	NM_001252102.2(KIF21B):c.2677C>T (p.Arg893Cys)	KIF21B (R893C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530503	NM_001252102.2(KIF21B):c.772C>A (p.Pro258Thr)	KIF21B (P258T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527726	NM_001252102.2(KIF21B):c.3607A>T (p.Ser1203Cys)	KIF21B (S1203C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523075	NM_001252102.2(KIF21B):c.710G>A (p.Arg237His)	KIF21B (R237H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2506681	NM_001252102.2(KIF21B):c.1063A>G (p.Met355Val)	KIF21B (M355V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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