56992[Gene ID] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3288305	NM_020242.3(KIF15):c.11G>A (p.Gly4Asp)	KIF15 (G4D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2653725	NM_020242.3(KIF15):c.36G>A (p.Val12=)	KIF15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2542519	NM_020242.3(KIF15):c.63T>G (p.Ser21Arg)	KIF15 (S21R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604668	NM_020242.3(KIF15):c.75T>A (p.Asp25Glu)	KIF15 (D25E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1695966	NM_020242.3(KIF15):c.94C>T (p.Arg32Ter)	KIF15 (R32*)	Single nucleotide variant (nonsense)	Pulmonary fibrosis	GLikely risk allele
Select item 1695967	NM_020242.3(KIF15):c.95G>A (p.Arg32Gln)	KIF15 (R32Q)	Single nucleotide variant (missense variant)	Pulmonary fibrosis	GLikely risk allele
Select item 1695968	NM_020242.3(KIF15):c.164C>T (p.Ser55Phe)	KIF15 (S55F)	Single nucleotide variant (missense variant)	Pulmonary fibrosis	GLikely risk allele
Select item 2347809	NM_020242.3(KIF15):c.170C>T (p.Thr57Met)	KIF15 (T57M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114477	NM_020242.3(KIF15):c.212C>T (p.Thr71Met)	KIF15 (T71M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 1695929	NM_020242.3(KIF15):c.247-1_248del	KIF15	Deletion (splice acceptor variant)	Pulmonary fibrosis	GLikely risk allele
Select item 3114480	NM_020242.3(KIF15):c.258C>T (p.Phe86=)	KIF15	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2407713	NM_020242.3(KIF15):c.292A>G (p.Met98Val)	KIF15 (M98V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239288	NM_020242.3(KIF15):c.355A>G (p.Met119Val)	KIF15 (M119V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1695969	NM_020242.3(KIF15):c.362-1G>A	KIF15	Single nucleotide variant (splice acceptor variant)	Pulmonary fibrosis	GLikely risk allele
Select item 1695970	NM_020242.3(KIF15):c.409C>T (p.Pro137Ser)	KIF15 (P137S)	Single nucleotide variant (missense variant)	Pulmonary fibrosis	GLikely risk allele
Select item 3114487	NM_020242.3(KIF15):c.413G>A (p.Arg138Gln)	KIF15 (R138Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 746987	NM_020242.3(KIF15):c.485G>C (p.Cys162Ser)	KIF15 (C162S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1695930	NM_020242.3(KIF15):c.539_540del (p.Ser180fs)	KIF15 (S180fs)	Microsatellite (frameshift variant)	Pulmonary fibrosis	GLikely risk allele
Select item 3114488	NM_020242.3(KIF15):c.595G>A (p.Gly199Ser)	KIF15 (G199S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 717832	NM_020242.3(KIF15):c.632C>T (p.Ala211Val)	KIF15 (A211V)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1678301	NM_020242.3(KIF15):c.660G>T (p.Arg220Ser)	KIF15 (R220S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3288301	NM_020242.3(KIF15):c.668G>A (p.Arg223His)	KIF15 (R223H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1695971	NM_020242.3(KIF15):c.673G>A (p.Ala225Thr)	KIF15 (A225T)	Single nucleotide variant (missense variant)	Pulmonary fibrosis	GLikely risk allele
Select item 2204880	NM_020242.3(KIF15):c.685A>G (p.Met229Val)	KIF15 (M229V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 872541	NM_020242.3(KIF15):c.715G>A (p.Val239Ile)	KIF15 (V239I)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2319492	NM_020242.3(KIF15):c.950A>G (p.Asp317Gly)	KIF15 (D317G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288307	NM_020242.3(KIF15):c.969A>C (p.Leu323Phe)	KIF15 (L323F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221904	NM_020242.3(KIF15):c.1058C>T (p.Thr353Ile)	KIF15 (T353I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285568	NM_020242.3(KIF15):c.1075A>G (p.Arg359Gly)	KIF15 (R359G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486692	NM_020242.3(KIF15):c.1102G>A (p.Val368Ile)	KIF15 (V368I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 722578	NM_020242.3(KIF15):c.1176G>C (p.Ala392=)	KIF15	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 778067	NM_020242.3(KIF15):c.1224C>A (p.Asp408Glu)	KIF15 (D408E)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3288308	NM_020242.3(KIF15):c.1288C>G (p.Gln430Glu)	KIF15 (Q430E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279557	NM_020242.3(KIF15):c.1405C>T (p.Arg469Cys)	KIF15 (R469C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 778068	NM_020242.3(KIF15):c.1483A>G (p.Asn495Asp)	KIF15 (N495D)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1698455	NM_020242.3(KIF15):c.1501C>T (p.Arg501Ter)	KIF15 (R501*)	Single nucleotide variant (nonsense)	Braddock-carey syndrome 2	GPathogenic
Select item 1695931	NM_020242.3(KIF15):c.1580_1581del (p.Leu527fs)	KIF15 (L527fs)	Deletion (frameshift variant)	Pulmonary fibrosis	GLikely risk allele
Select item 3114473	NM_020242.3(KIF15):c.1628C>G (p.Thr543Ser)	KIF15 (T543S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3341372	NM_020242.3(KIF15):c.1654T>C (p.Ser552Pro)	KIF15 (S552P)	Single nucleotide variant (missense variant)	Braddock-carey syndrome 2	GUncertain significance
Select item 3025072	NM_020242.3(KIF15):c.1767G>C (p.Leu589=)	KIF15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3065669	NM_020242.3(KIF15):c.1830-2A>C	KIF15	Single nucleotide variant (splice acceptor variant)	Braddock-carey syndrome 2	GLikely pathogenic
Select item 3025261	NM_020242.3(KIF15):c.1865C>T (p.Ser622Phe)	KIF15 (S622F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3114474	NM_020242.3(KIF15):c.1903G>A (p.Glu635Lys)	KIF15 (E635K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114475	NM_020242.3(KIF15):c.1909A>G (p.Thr637Ala)	KIF15 (T637A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333959	NM_020242.3(KIF15):c.1962A>T (p.Glu654Asp)	KIF15 (E654D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278770	NM_020242.3(KIF15):c.2077A>G (p.Ile693Val)	KIF15 (I693V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114478	NM_020242.3(KIF15):c.2144T>C (p.Ile715Thr)	KIF15 (I715T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 787783	NM_020242.3(KIF15):c.2278-7C>T	KIF15	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 773571	NM_020242.3(KIF15):c.2325T>G (p.Leu775=)	KIF15	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3114479	NM_020242.3(KIF15):c.2329T>C (p.Ser777Pro)	KIF15 (S777P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288303	NM_020242.3(KIF15):c.2337G>C (p.Leu779Phe)	KIF15 (L779F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238567	NM_020242.3(KIF15):c.2419C>T (p.Leu807Phe)	KIF15 (L807F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331820	NM_020242.3(KIF15):c.2428G>A (p.Ala810Thr)	KIF15 (A810T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345885	NM_020242.3(KIF15):c.2477C>T (p.Thr826Met)	KIF15 (T826M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 724083	NM_020242.3(KIF15):c.2477C>G (p.Thr826Arg)	KIF15 (T826R)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 767899	NM_020242.3(KIF15):c.2480A>G (p.Asn827Ser)	KIF15 (N827S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2538105	NM_020242.3(KIF15):c.2491G>A (p.Glu831Lys)	KIF15 (E831K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288302	NM_020242.3(KIF15):c.2527C>A (p.Gln843Lys)	KIF15 (Q843K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2653726	NM_020242.3(KIF15):c.2530C>G (p.Leu844Val)	KIF15 (L844V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 791922	NM_020242.3(KIF15):c.2550-6A>G	KIF15	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1678302	NM_020242.3(KIF15):c.2611C>T (p.Gln871Ter)	KIF15 (Q871*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 767900	NM_020242.3(KIF15):c.2611C>G (p.Gln871Glu)	KIF15 (Q871E)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3288304	NM_020242.3(KIF15):c.2634T>G (p.Ile878Met)	KIF15 (I878M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539887	NM_020242.3(KIF15):c.2701A>C (p.Asn901His)	KIF15 (N901H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288309	NM_020242.3(KIF15):c.2738A>G (p.Asn913Ser)	KIF15 (N913S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114481	NM_020242.3(KIF15):c.2812G>A (p.Val938Ile)	KIF15 (V938I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340013	NM_020242.3(KIF15):c.2816G>A (p.Arg939His)	KIF15 (R939H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114482	NM_020242.3(KIF15):c.3005C>T (p.Thr1002Ile)	KIF15 (T1002I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 791923	NM_020242.3(KIF15):c.3049-7T>C	KIF15	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2373453	NM_020242.3(KIF15):c.3108G>C (p.Gln1036His)	KIF15 (Q1036H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 767901	NM_020242.3(KIF15):c.3111A>G (p.Glu1037=)	KIF15	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1695932	NM_020242.3(KIF15):c.3158_3159del (p.Leu1052_Ser1053insTer)	KIF15	Deletion (nonsense)	Pulmonary fibrosis	GLikely risk allele
Select item 3114483	NM_020242.3(KIF15):c.3175G>A (p.Asp1059Asn)	KIF15 (D1059N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 774841	NM_020242.3(KIF15):c.3248C>T (p.Ser1083Leu)	KIF15 (S1083L)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2405950	NM_020242.3(KIF15):c.3251G>A (p.Gly1084Glu)	KIF15 (G1084E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528902	NM_020242.3(KIF15):c.3281C>T (p.Thr1094Ile)	KIF15 (T1094I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 872542	NM_020242.3(KIF15):c.3359A>G (p.Glu1120Gly)	KIF15 (E1120G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3114484	NM_020242.3(KIF15):c.3400T>C (p.Ser1134Pro)	KIF15 (S1134P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1695919	NM_020242.3(KIF15):c.3421-2A>G	KIF15	Single nucleotide variant (splice acceptor variant)	Pulmonary fibrosis	GLikely risk allele
Select item 767902	NM_020242.3(KIF15):c.3441C>G (p.His1147Gln)	KIF15 (H1147Q)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2611109	NM_020242.3(KIF15):c.3463C>T (p.Leu1155Phe)	KIF15 (L1155F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114485	NM_020242.3(KIF15):c.3475C>G (p.Gln1159Glu)	KIF15 (Q1159E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3114486	NM_020242.3(KIF15):c.3527T>C (p.Leu1176Pro)	KIF15 (L1176P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276510	NM_020242.3(KIF15):c.3613C>T (p.Arg1205Cys)	KIF15 (R1205C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400857	NM_020242.3(KIF15):c.3614G>T (p.Arg1205Leu)	KIF15 (R1205L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607229	NM_020242.3(KIF15):c.3620A>G (p.Glu1207Gly)	KIF15 (E1207G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288306	NM_020242.3(KIF15):c.3622A>C (p.Ser1208Arg)	KIF15 (S1208R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366543	NM_020242.3(KIF15):c.3634A>G (p.Ile1212Val)	KIF15 (I1212V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330148	NM_020242.3(KIF15):c.3674T>A (p.Ile1225Asn)	KIF15 (I1225N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533368	NM_020242.3(KIF15):c.3734A>C (p.Glu1245Ala)	KIF15 (E1245A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354942	NM_020242.3(KIF15):c.3736C>A (p.Gln1246Lys)	KIF15 (Q1246K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324839	NM_020242.3(KIF15):c.3815A>T (p.Glu1272Val)	KIF15 (E1272V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 767903	NM_020242.3(KIF15):c.3816A>C (p.Glu1272Asp)	KIF15 (E1272D)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3025508	NM_020242.3(KIF15):c.3863C>T (p.Thr1288Ile)	KIF15 (T1288I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2349383	NM_020242.3(KIF15):c.3874G>A (p.Glu1292Lys)	KIF15 (E1292K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 744297	NM_020242.3(KIF15):c.3877C>A (p.Arg1293=)	KIF15	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2221729	NM_020242.3(KIF15):c.4020T>G (p.Asn1340Lys)	KIF15 (N1340K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307006	NM_020242.3(KIF15):c.4029G>C (p.Leu1343Phe)	KIF15 (L1343F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327027	NM_020242.3(KIF15):c.4112A>G (p.Glu1371Gly)	KIF15 (E1371G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 725428	NM_020242.3(KIF15):c.4125C>T (p.Ala1375=)	KIF15	Single nucleotide variant (synonymous variant)	not provided	GBenign

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