ClinVar for Gene (Select 3796) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3375808	NM_001098511.3(KIF2A):c.797C>T (p.Thr266Ile)	KIF2A (T239I +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3372557	NM_001098511.3(KIF2A):c.202C>T (p.Pro68Ser)	KIF2A (P41S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3343306	NM_001098511.3(KIF2A):c.1162G>C (p.Glu388Gln)	KIF2A (E361Q +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3343006	NM_001098511.3(KIF2A):c.1153A>G (p.Arg385Gly)	KIF2A (R358G +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3256899	NM_001098511.3(KIF2A):c.1388G>A (p.Arg463Lys)	KIF2A (R436K +2 more)	Single nucleotide variant (missense variant)	Complex cortical dysplasia with other brain malformations 3	GUncertain significance
Select item 3251921	NM_001098511.3(KIF2A):c.669G>T (p.Arg223Ser)	KIF2A (R196S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3246464	NC_000005.9:g.(?_61673468)_(61681396_?)dup	KIF2A	Duplication	not provided	GLikely benign
Select item 3246462	NC_000005.9:g.(?_61668245)_(61673609_?)dup	KIF2A	Duplication	not provided	GUncertain significance
Select item 3246461	NC_000005.9:g.(?_61657049)_(61681396_?)dup	KIF2A	Duplication	not provided	GUncertain significance
Select item 3246460	NC_000005.9:g.(?_61602300)_(61602363_?)dup	KIF2A	Duplication	not provided	GLikely benign
Select item 3234930	NM_001098511.3(KIF2A):c.454C>T (p.Pro152Ser)	KIF2A (P125S +1 more)	Single nucleotide variant (missense variant +1 more)	Complex cortical dysplasia with other brain malformations 3	GUncertain significance
Select item 3068009	NM_001098511.3(KIF2A):c.334G>A (p.Val112Met)	KIF2A (V112M +1 more)	Single nucleotide variant (missense variant)	Complex cortical dysplasia with other brain malformations 3	GUncertain significance
Select item 3067764	NM_001098511.3(KIF2A):c.1796G>A (p.Gly599Asp)	KIF2A (G534D +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3053009	NM_001098511.3(KIF2A):c.27C>T (p.Ile9=)	KIF2A, LOC129993961	Single nucleotide variant (synonymous variant +1 more)	KIF2A-related disorder	GLikely benign
Select item 3026951	NM_001098511.3(KIF2A):c.665A>G (p.His222Arg)	KIF2A (H195R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3026137	NM_001098511.3(KIF2A):c.999T>C (p.Asp333=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3022518	NM_001098511.3(KIF2A):c.561C>T (p.Asp187=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3010654	NM_001098511.3(KIF2A):c.287G>A (p.Arg96Gln)	KIF2A (R96Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3010410	NM_001098511.3(KIF2A):c.559-18C>A	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3009852	NM_001098511.3(KIF2A):c.273T>A (p.Ile91=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3007531	NM_001098511.3(KIF2A):c.777A>C (p.Pro259=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3006739	NM_001098511.3(KIF2A):c.1646+19C>T	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3006492	NM_001098511.3(KIF2A):c.286C>T (p.Arg96Trp)	KIF2A (R69W +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3006314	NM_001098511.3(KIF2A):c.2044G>T (p.Ala682Ser)	KIF2A (A617S +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2994617	NM_001098511.3(KIF2A):c.1251C>T (p.Gly417=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2993470	NM_001098511.3(KIF2A):c.280-9C>T	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2991197	NM_001098511.3(KIF2A):c.280-15T>C	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2991196	NM_001098511.3(KIF2A):c.280-11del	KIF2A	Deletion (intron variant)	not provided	GBenign
Select item 2990862	NM_001098511.3(KIF2A):c.321A>G (p.Ser107=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2989709	NM_001098511.3(KIF2A):c.1539A>G (p.Leu513=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2987050	NM_001098511.3(KIF2A):c.709+15G>A	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2986050	NM_001098511.3(KIF2A):c.2013+7T>A	KIF2A	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2985853	NM_001098511.3(KIF2A):c.1239C>T (p.Leu413=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2984406	NM_001098511.3(KIF2A):c.1646+7G>C	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2983997	NM_001098511.3(KIF2A):c.1732T>C (p.Tyr578His)	KIF2A (Y578H)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2978990	NM_001098511.3(KIF2A):c.807A>G (p.Leu269=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2978598	NM_001098511.3(KIF2A):c.2020A>G (p.Ile674Val)	KIF2A (I609V +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2975065	NM_001098511.3(KIF2A):c.2014-17A>G	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2973896	NM_001098511.3(KIF2A):c.901A>G (p.Ile301Val)	KIF2A (I282V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2973278	NM_001098511.3(KIF2A):c.612T>C (p.Phe204=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2967702	NM_001098511.3(KIF2A):c.660T>C (p.Asp220=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2965389	NM_001098511.3(KIF2A):c.206A>G (p.Asp69Gly)	KIF2A (D42G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2964637	NM_001098511.3(KIF2A):c.1527C>T (p.Leu509=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2964419	NM_001098511.3(KIF2A):c.280-4A>G	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2956593	NM_001098511.3(KIF2A):c.2058G>A (p.Met686Ile)	KIF2A (M686I +3 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2917201	NM_001098511.3(KIF2A):c.1923C>A (p.Val641=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2883682	NM_001098511.3(KIF2A):c.335-6T>C	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2881042	NM_001098511.3(KIF2A):c.1827A>G (p.Pro609=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2880432	NM_001098511.3(KIF2A):c.464G>A (p.Arg155Lys)	KIF2A (R136K +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2874744	NM_001098511.3(KIF2A):c.65-7C>T	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2873598	NM_001098511.3(KIF2A):c.1230A>G (p.Val410=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2865487	NM_001098511.3(KIF2A):c.306G>A (p.Lys102=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2865428	NM_001098511.3(KIF2A):c.873-16G>A	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2864438	NM_001098511.3(KIF2A):c.1646+7G>A	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2859957	NM_001098511.3(KIF2A):c.1893A>G (p.Lys631=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2858676	NM_001098511.3(KIF2A):c.1386A>G (p.Glu462=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2853438	NM_001098511.3(KIF2A):c.912G>A (p.Arg304=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2849864	NM_001098511.3(KIF2A):c.335-20T>G	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2849839	NM_001098511.3(KIF2A):c.2023C>T (p.Arg675Trp)	KIF2A (R610W +3 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2849764	NM_001098511.3(KIF2A):c.1579-17T>A	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2845760	NM_001098511.3(KIF2A):c.448G>A (p.Gly150Arg)	KIF2A (G123R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2845199	NM_001098511.3(KIF2A):c.1760+11T>C	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2844957	NM_001098511.3(KIF2A):c.196C>T (p.Leu66Phe)	KIF2A (L39F +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2844020	NM_001098511.3(KIF2A):c.1348C>T (p.His450Tyr)	KIF2A (H431Y +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2842552	NM_001098511.3(KIF2A):c.602T>A (p.Ile201Asn)	KIF2A (I182N +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2840540	NM_001098511.3(KIF2A):c.726T>G (p.Asp242Glu)	KIF2A (D215E +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2838691	NM_001098511.3(KIF2A):c.1467+11T>C	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2836164	NM_001098511.3(KIF2A):c.654+10T>A	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2835578	NM_001098511.3(KIF2A):c.713C>G (p.Thr238Ser)	KIF2A (T238S +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2827788	NM_001098511.3(KIF2A):c.559-10C>A	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2827528	NM_001098511.3(KIF2A):c.1624A>T (p.Asn542Tyr)	KIF2A (N515Y +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2821405	NM_001098511.3(KIF2A):c.562G>T (p.Val188Phe)	KIF2A (V161F +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2819352	NM_001098511.3(KIF2A):c.558+9C>T	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2818062	NM_001098511.3(KIF2A):c.1119G>A (p.Lys373=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2812088	NM_001098511.3(KIF2A):c.872+4G>A	KIF2A	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2811558	NM_001098511.3(KIF2A):c.1760+3del	KIF2A	Deletion (intron variant)	not provided	GUncertain significance
Select item 2806144	NM_001098511.3(KIF2A):c.160-7T>C	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2805625	NM_001098511.3(KIF2A):c.395A>G (p.Gln132Arg)	KIF2A (Q105R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2805177	NM_001098511.3(KIF2A):c.924A>G (p.Thr308=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2803873	NM_001098511.3(KIF2A):c.2148G>A (p.Arg716=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2800393	NM_001098511.3(KIF2A):c.1977A>G (p.Glu659=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2796280	NM_001098511.3(KIF2A):c.19G>A (p.Gly7Ser)	LOC129993961, KIF2A (G7S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2793430	NM_001098511.3(KIF2A):c.37A>G (p.Ile13Val)	KIF2A, LOC129993961 (I13V)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2789314	NM_001098511.3(KIF2A):c.1119+15T>A	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2785898	NM_001098511.3(KIF2A):c.1579-6C>T	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2783045	NM_001098511.3(KIF2A):c.872+10T>C	KIF2A	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2782203	NM_001098511.3(KIF2A):c.247G>T (p.Ala83Ser)	KIF2A (A56S +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2773011	NM_001098511.3(KIF2A):c.1112G>C (p.Ser371Thr)	KIF2A (S352T +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2769822	NM_001098511.3(KIF2A):c.1870T>A (p.Ser624Thr)	KIF2A (S559T +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2769044	NM_001098511.3(KIF2A):c.1319A>G (p.Gln440Arg)	KIF2A (Q413R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2763131	NM_001098511.3(KIF2A):c.1741T>A (p.Phe581Ile)	KIF2A (F581I)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2757959	NM_001098511.3(KIF2A):c.1433G>C (p.Gly478Ala)	KIF2A (G459A +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2757539	NM_001098511.3(KIF2A):c.2213C>G (p.Pro738Arg)	KIF2A (P700R +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2757449	NM_001098511.3(KIF2A):c.1808C>T (p.Pro603Leu)	KIF2A (P538L +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2757443	NM_001098511.3(KIF2A):c.1650A>C (p.Val550=)	KIF2A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2749241	NM_001098511.3(KIF2A):c.2146C>A (p.Arg716=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2747917	NM_001098511.3(KIF2A):c.579A>G (p.Pro193=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2746864	NM_001098511.3(KIF2A):c.1193G>T (p.Gly398Val)	KIF2A (G398V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2743426	NM_001098511.3(KIF2A):c.1547C>G (p.Ser516Cys)	KIF2A (S489C +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2729885	NM_001098511.3(KIF2A):c.1572C>G (p.Thr524=)	KIF2A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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