ClinVar for Gene (Select 26153) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3233662	NM_015656.2(KIF26A):c.4378del (p.Arg1460fs)	KIF26A (R1460fs)	Deletion (frameshift variant)	Cortical dysplasia, complex, with other brain malformations 11	GPathogenic
Select item 3114790	NM_015656.2(KIF26A):c.992G>A (p.Arg331His)	KIF26A (R331H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114789	NM_015656.2(KIF26A):c.904G>T (p.Ala302Ser)	KIF26A (A302S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114788	NM_015656.2(KIF26A):c.799G>A (p.Gly267Ser)	KIF26A (G267S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114787	NM_015656.2(KIF26A):c.725C>T (p.Pro242Leu)	KIF26A (P242L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114786	NM_015656.2(KIF26A):c.703C>T (p.Arg235Trp)	KIF26A (R235W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114785	NM_015656.2(KIF26A):c.584T>C (p.Leu195Pro)	KIF26A (L195P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114784	NM_015656.2(KIF26A):c.5644G>A (p.Val1882Ile)	KIF26A (V1882I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114783	NM_015656.2(KIF26A):c.5633A>G (p.Gln1878Arg)	KIF26A (Q1878R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114782	NM_015656.2(KIF26A):c.5432G>A (p.Arg1811Gln)	KIF26A (R1811Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114780	NM_015656.2(KIF26A):c.536C>T (p.Pro179Leu)	KIF26A (P179L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114779	NM_015656.2(KIF26A):c.5369G>A (p.Arg1790Gln)	KIF26A (R1790Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114778	NM_015656.2(KIF26A):c.5287C>T (p.Arg1763Cys)	KIF26A (R1763C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114777	NM_015656.2(KIF26A):c.5275C>T (p.Leu1759Phe)	KIF26A (L1759F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114776	NM_015656.2(KIF26A):c.5272C>T (p.Arg1758Cys)	KIF26A (R1758C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114775	NM_015656.2(KIF26A):c.5198A>G (p.Asp1733Gly)	KIF26A (D1733G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114774	NM_015656.2(KIF26A):c.5140C>T (p.Pro1714Ser)	KIF26A (P1714S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114773	NM_015656.2(KIF26A):c.5119C>T (p.Arg1707Trp)	KIF26A (R1707W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114772	NM_015656.2(KIF26A):c.4994G>A (p.Arg1665His)	KIF26A (R1665H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114771	NM_015656.2(KIF26A):c.4993C>T (p.Arg1665Cys)	KIF26A (R1665C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114770	NM_015656.2(KIF26A):c.4963G>A (p.Gly1655Ser)	KIF26A (G1655S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114769	NM_015656.2(KIF26A):c.4862G>A (p.Arg1621Gln)	KIF26A (R1621Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114768	NM_015656.2(KIF26A):c.4814C>A (p.Thr1605Lys)	KIF26A (T1605K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114767	NM_015656.2(KIF26A):c.4777G>C (p.Asp1593His)	KIF26A (D1593H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114766	NM_015656.2(KIF26A):c.4705G>C (p.Glu1569Gln)	KIF26A (E1569Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114765	NM_015656.2(KIF26A):c.4648C>T (p.Arg1550Trp)	KIF26A (R1550W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114764	NM_015656.2(KIF26A):c.4525C>T (p.Arg1509Trp)	KIF26A (R1509W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114763	NM_015656.2(KIF26A):c.4318C>T (p.Arg1440Trp)	KIF26A (R1440W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114762	NM_015656.2(KIF26A):c.4306G>C (p.Ala1436Pro)	KIF26A (A1436P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114760	NM_015656.2(KIF26A):c.4193G>A (p.Gly1398Glu)	KIF26A (G1398E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114759	NM_015656.2(KIF26A):c.4178C>T (p.Ala1393Val)	KIF26A (A1393V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114758	NM_015656.2(KIF26A):c.4079C>T (p.Ala1360Val)	KIF26A (A1360V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114757	NM_015656.2(KIF26A):c.4076C>T (p.Ala1359Val)	KIF26A (A1359V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114756	NM_015656.2(KIF26A):c.4001G>A (p.Gly1334Glu)	KIF26A (G1334E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114755	NM_015656.2(KIF26A):c.3958G>C (p.Val1320Leu)	KIF26A (V1320L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114754	NM_015656.2(KIF26A):c.3950C>T (p.Thr1317Met)	KIF26A (T1317M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114753	NM_015656.2(KIF26A):c.3883C>T (p.Arg1295Cys)	KIF26A (R1295C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114752	NM_015656.2(KIF26A):c.3878C>T (p.Ala1293Val)	KIF26A (A1293V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114751	NM_015656.2(KIF26A):c.3805C>T (p.Arg1269Trp)	KIF26A (R1269W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114749	NM_015656.2(KIF26A):c.3787C>T (p.Pro1263Ser)	KIF26A (P1263S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114748	NM_015656.2(KIF26A):c.3703C>T (p.Arg1235Cys)	KIF26A (R1235C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114747	NM_015656.2(KIF26A):c.3664C>A (p.Arg1222Ser)	KIF26A (R1222S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114746	NM_015656.2(KIF26A):c.3634C>T (p.Arg1212Trp)	KIF26A (R1212W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114745	NM_015656.2(KIF26A):c.353G>A (p.Arg118His)	KIF26A (R118H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114744	NM_015656.2(KIF26A):c.3367G>A (p.Asp1123Asn)	KIF26A (D1123N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114743	NM_015656.2(KIF26A):c.3283C>G (p.Pro1095Ala)	KIF26A (P1095A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114742	NM_015656.2(KIF26A):c.3278G>A (p.Gly1093Glu)	KIF26A (G1093E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114741	NM_015656.2(KIF26A):c.3020G>A (p.Arg1007His)	KIF26A (R1007H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3114740	NM_015656.2(KIF26A):c.2852C>T (p.Pro951Leu)	KIF26A (P951L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114739	NM_015656.2(KIF26A):c.2584G>A (p.Gly862Ser)	KIF26A (G862S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114738	NM_015656.2(KIF26A):c.2485G>C (p.Gly829Arg)	KIF26A (G829R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114737	NM_015656.2(KIF26A):c.2480C>A (p.Ser827Tyr)	KIF26A (S827Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114736	NM_015656.2(KIF26A):c.2466C>G (p.Ser822Arg)	KIF26A (S822R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114735	NM_015656.2(KIF26A):c.2323G>A (p.Gly775Ser)	KIF26A (G775S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114734	NM_015656.2(KIF26A):c.2169C>G (p.His723Gln)	KIF26A (H723Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114733	NM_015656.2(KIF26A):c.2146G>A (p.Val716Met)	KIF26A (V716M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114732	NM_015656.2(KIF26A):c.2137C>T (p.Leu713Phe)	KIF26A (L713F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114731	NM_015656.2(KIF26A):c.2116C>A (p.Pro706Thr)	KIF26A (P706T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114730	NM_015656.2(KIF26A):c.2083C>T (p.Arg695Cys)	KIF26A (R695C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114728	NM_015656.2(KIF26A):c.1928G>A (p.Gly643Asp)	KIF26A (G643D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114727	NM_015656.2(KIF26A):c.1885C>T (p.Arg629Cys)	KIF26A (R629C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114726	NM_015656.2(KIF26A):c.1828G>A (p.Val610Ile)	KIF26A (V610I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114725	NM_015656.2(KIF26A):c.1804T>G (p.Ser602Ala)	KIF26A (S602A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114724	NM_015656.2(KIF26A):c.1801A>G (p.Ser601Gly)	KIF26A (S601G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114723	NM_015656.2(KIF26A):c.1705C>T (p.Arg569Trp)	KIF26A (R569W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114722	NM_015656.2(KIF26A):c.1592G>A (p.Arg531Gln)	KIF26A (R531Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114721	NM_015656.2(KIF26A):c.1367C>T (p.Ser456Leu)	KIF26A (S456L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114720	NM_015656.2(KIF26A):c.1231G>C (p.Gly411Arg)	KIF26A (G411R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114718	NM_015656.2(KIF26A):c.1027G>T (p.Val343Phe)	KIF26A (V343F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3064895	NM_015656.2(KIF26A):c.4979_4980del (p.Gly1659_Tyr1660insTer)	KIF26A	Deletion (nonsense)	Cortical dysplasia, complex, with other brain malformations 11	GLikely pathogenic
Select item 3063628	NM_015656.2(KIF26A):c.5297C>T (p.Pro1766Leu)	KIF26A (P1766L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063327	GRCh37/hg19 14q32.31-32.33(chr14:102098959-107285437)x1	ADSS1, AHNAK2 +65 more	Copy number loss	not specified	GPathogenic
Select item 3026302	NM_015656.2(KIF26A):c.3957T>C (p.Ala1319=)	KIF26A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2685500	GRCh37/hg19 14q32.2-32.33(chr14:101024609-107285437)x1	DIO3OS, WDR20 +91 more	Copy number loss	not provided	GPathogenic
Select item 2684743	GRCh37/hg19 14q31.3-32.33(chr14:88580184-107285437)x3	ADSS1, AHNAK2 +182 more	Copy number gain	not provided	GPathogenic
Select item 2684728	GRCh37/hg19 14q23.1-32.33(chr14:58894502-107227240)x3	ACOT4, ACOT6 +353 more	Copy number gain	not provided	GPathogenic
Select item 2683901	NM_015656.2(KIF26A):c.4085dup (p.Ala1363fs)	KIF26A (A1363fs)	Duplication (frameshift variant)	Cortical dysplasia, complex, with other brain malformations 11	GPathogenic
Select item 2681352	NM_015656.2(KIF26A):c.2642C>A (p.Pro881Gln)	KIF26A (P881Q)	Single nucleotide variant (missense variant)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2671916	NM_015656.2(KIF26A):c.3335C>T (p.Ser1112Phe)	KIF26A (S1112F)	Single nucleotide variant (missense variant)	Cortical dysplasia, complex, with other brain malformations 11	GUncertain significance
Select item 2644614	NM_015656.2(KIF26A):c.5628G>T (p.Gly1876=)	KIF26A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2644613	NM_015656.2(KIF26A):c.5514G>A (p.Ala1838=)	KIF26A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2644612	NM_015656.2(KIF26A):c.5148C>T (p.Pro1716=)	KIF26A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2644611	NM_015656.2(KIF26A):c.4794G>A (p.Val1598=)	KIF26A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2644610	NM_015656.2(KIF26A):c.4782C>T (p.Ser1594=)	KIF26A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2644609	NM_015656.2(KIF26A):c.4770C>T (p.Ser1590=)	KIF26A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2644608	NM_015656.2(KIF26A):c.3856G>A (p.Gly1286Arg)	KIF26A (G1286R)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2644607	NM_015656.2(KIF26A):c.3402C>T (p.Ser1134=)	KIF26A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2644606	NM_015656.2(KIF26A):c.2943C>T (p.Pro981=)	KIF26A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2644605	NM_015656.2(KIF26A):c.2238C>T (p.Gly746=)	KIF26A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2644604	NM_015656.2(KIF26A):c.1945G>A (p.Ala649Thr)	KIF26A (A649T)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2644603	NM_015656.2(KIF26A):c.1731T>C (p.Ala577=)	KIF26A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2644602	NM_015656.2(KIF26A):c.1545C>T (p.Ser515=)	KIF26A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2644601	NM_015656.2(KIF26A):c.1545C>G (p.Ser515=)	KIF26A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2644600	NM_015656.2(KIF26A):c.987C>T (p.Ala329=)	KIF26A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2644599	NM_015656.2(KIF26A):c.846G>A (p.Thr282=)	KIF26A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2644598	NM_015656.2(KIF26A):c.384C>T (p.Cys128=)	KIF26A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2644597	NM_015656.2(KIF26A):c.363C>T (p.Ala121=)	KIF26A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2644596	NM_015656.2(KIF26A):c.60G>A (p.Pro20=)	KIF26A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2627109	NM_015656.2(KIF26A):c.3996C>A (p.Cys1332Ter)	KIF26A (C1332*)	Single nucleotide variant (nonsense)	Cortical dysplasia, complex, with other brain malformations 11	GLikely pathogenic
Select item 2616855	NM_015656.2(KIF26A):c.3665G>C (p.Arg1222Pro)	KIF26A (R1222P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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