ClinVar for Gene (Select 197335) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3338188	NM_145294.5(WDR90):c.4489C>T (p.Arg1497Trp)	WDR90 (R1497W)	Single nucleotide variant (missense variant)	Autism	GUncertain significance
Select item 3333022	NM_145294.5(WDR90):c.3986G>A (p.Arg1329His)	WDR90 (R1329H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333019	NM_145294.5(WDR90):c.4241C>T (p.Ala1414Val)	WDR90 (A1414V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333018	NM_145294.5(WDR90):c.5086G>T (p.Ala1696Ser)	WDR90 (A1696S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333017	NM_145294.5(WDR90):c.2902A>G (p.Ile968Val)	WDR90 (I968V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333016	NM_145294.5(WDR90):c.967T>C (p.Ser323Pro)	WDR90 (S323P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333015	NM_145294.5(WDR90):c.1309C>T (p.Leu437Phe)	WDR90 (L437F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333014	NM_145294.5(WDR90):c.1720T>A (p.Phe574Ile)	WDR90 (F574I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333013	NM_145294.5(WDR90):c.3122A>G (p.Lys1041Arg)	WDR90 (K1041R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333012	NM_145294.5(WDR90):c.3415C>T (p.Arg1139Cys)	WDR90 (R1139C)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3333011	NM_145294.5(WDR90):c.1766G>A (p.Arg589His)	WDR90 (R589H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333010	NM_145294.5(WDR90):c.1546G>A (p.Asp516Asn)	WDR90 (D516N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333008	NM_145294.5(WDR90):c.2537G>A (p.Arg846His)	WDR90 (R846H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333007	NM_145294.5(WDR90):c.3868C>G (p.Arg1290Gly)	WDR90 (R1290G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333006	NM_145294.5(WDR90):c.1777C>T (p.Arg593Trp)	WDR90 (R593W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333005	NM_145294.5(WDR90):c.1981G>A (p.Val661Ile)	WDR90 (V661I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3333004	NM_145294.5(WDR90):c.2465G>C (p.Arg822Pro)	WDR90 (R822P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333003	NM_145294.5(WDR90):c.3752C>T (p.Pro1251Leu)	WDR90 (P1251L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3243622	NC_000016.9:g.(?_256302)_(1557737_?)del	TELO2, STUB1 +53 more	Deletion	not provided	GPathogenic
Select item 3243338	NC_000016.9:g.(?_396128)_(1204056_?)dup	ANTKMT, AXIN1 +34 more	Duplication	Idiopathic generalized epilepsy +1 more	GUncertain significance
Select item 3243222	NC_000016.9:g.(?_339420)_(3767509_?)dup	ABCA3, AMDHD2 +142 more	Duplication	Idiopathic generalized epilepsy +2 more	GUncertain significance
Select item 3190405	NM_145294.5(WDR90):c.5239G>A (p.Gly1747Ser)	WDR90 (G1747S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190404	NM_145294.5(WDR90):c.5026C>A (p.Pro1676Thr)	WDR90 (P1676T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190403	NM_145294.5(WDR90):c.481G>A (p.Gly161Ser)	WDR90 (G161S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190402	NM_145294.5(WDR90):c.4450G>T (p.Ala1484Ser)	WDR90 (A1484S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190401	NM_145294.5(WDR90):c.4445G>T (p.Cys1482Phe)	WDR90 (C1482F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190400	NM_145294.5(WDR90):c.4423G>T (p.Val1475Leu)	WDR90 (V1475L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190399	NM_145294.5(WDR90):c.4346A>G (p.His1449Arg)	WDR90 (H1449R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190398	NM_145294.5(WDR90):c.4130A>G (p.Lys1377Arg)	WDR90 (K1377R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190397	NM_145294.5(WDR90):c.4085G>A (p.Arg1362Gln)	WDR90 (R1362Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190396	NM_145294.5(WDR90):c.4024G>A (p.Gly1342Ser)	WDR90 (G1342S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190395	NM_145294.5(WDR90):c.3991G>A (p.Gly1331Ser)	WDR90 (G1331S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190394	NM_145294.5(WDR90):c.3806G>A (p.Gly1269Asp)	WDR90 (G1269D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190393	NM_145294.5(WDR90):c.3784G>T (p.Ala1262Ser)	WDR90 (A1262S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190392	NM_145294.5(WDR90):c.3746C>T (p.Pro1249Leu)	WDR90 (P1249L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190391	NM_145294.5(WDR90):c.3362G>A (p.Arg1121Gln)	WDR90 (R1121Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190390	NM_145294.5(WDR90):c.3307G>A (p.Ala1103Thr)	WDR90 (A1103T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190389	NM_145294.5(WDR90):c.3217C>G (p.Arg1073Gly)	WDR90 (R1073G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190388	NM_145294.5(WDR90):c.3175G>A (p.Gly1059Ser)	WDR90 (G1059S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190387	NM_145294.5(WDR90):c.2966C>T (p.Ala989Val)	WDR90 (A989V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190386	NM_145294.5(WDR90):c.2912C>T (p.Ser971Leu)	WDR90 (S971L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190385	NM_145294.5(WDR90):c.278A>G (p.Lys93Arg)	WDR90 (K93R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190384	NM_145294.5(WDR90):c.2663T>C (p.Met888Thr)	WDR90 (M888T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190383	NM_145294.5(WDR90):c.2385C>G (p.Asp795Glu)	WDR90 (D795E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190381	NM_145294.5(WDR90):c.2239G>A (p.Ala747Thr)	WDR90 (A747T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190380	NM_145294.5(WDR90):c.2068C>T (p.Arg690Trp)	WDR90 (R690W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190379	NM_145294.5(WDR90):c.202A>G (p.Thr68Ala)	WDR90 (T68A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190378	NM_145294.5(WDR90):c.2014C>T (p.Arg672Cys)	WDR90 (R672C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190377	NM_145294.5(WDR90):c.1789C>T (p.Arg597Cys)	WDR90 (R597C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190376	NM_145294.5(WDR90):c.1768A>G (p.Met590Val)	WDR90 (M590V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190375	NM_145294.5(WDR90):c.1754T>C (p.Ile585Thr)	WDR90 (I585T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190374	NM_145294.5(WDR90):c.172C>T (p.Pro58Ser)	WDR90 (P58S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190373	NM_145294.5(WDR90):c.1580G>C (p.Ser527Thr)	WDR90 (S527T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190372	NM_145294.5(WDR90):c.1502C>T (p.Ala501Val)	WDR90 (A501V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190371	NM_145294.5(WDR90):c.1393G>A (p.Gly465Arg)	WDR90 (G465R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2685536	GRCh37/hg19 16p13.3(chr16:85881-1657611)x1	PRR35, ANTKMT +65 more	Copy number loss	not provided	GPathogenic
Select item 2645842	NM_145294.5(WDR90):c.5154C>T (p.Asn1718=)	WDR90	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645841	NM_145294.5(WDR90):c.3990C>T (p.Ala1330=)	WDR90	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645840	NM_145294.5(WDR90):c.3831C>G (p.Leu1277=)	WDR90	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645839	NM_145294.5(WDR90):c.3060C>T (p.Gly1020=)	WDR90	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645838	NM_145294.5(WDR90):c.1594C>A (p.Arg532=)	WDR90	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645837	NM_145294.5(WDR90):c.1089C>T (p.Gly363=)	WDR90	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645836	NM_145294.5(WDR90):c.687G>T (p.Leu229Phe)	WDR90 (L229F)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2645835	NM_145294.5(WDR90):c.560-7C>T	WDR90	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2624047	NM_145294.5(WDR90):c.4262G>C (p.Ser1421Thr)	WDR90 (S1421T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620405	NM_145294.5(WDR90):c.2423T>C (p.Leu808Pro)	WDR90 (L808P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618934	NM_145294.5(WDR90):c.3898G>A (p.Ala1300Thr)	WDR90 (A1300T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615216	NM_145294.5(WDR90):c.185C>T (p.Thr62Ile)	WDR90 (T62I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609477	NM_145294.5(WDR90):c.2620A>G (p.Ile874Val)	WDR90 (I874V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2603857	NM_145294.5(WDR90):c.3227A>C (p.Tyr1076Ser)	WDR90 (Y1076S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600812	NM_145294.5(WDR90):c.1951G>A (p.Val651Met)	WDR90 (V651M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598698	NM_145294.5(WDR90):c.4193G>A (p.Ser1398Asn)	WDR90 (S1398N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598256	NM_145294.5(WDR90):c.22C>T (p.Pro8Ser)	WDR90 (P8S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598244	NM_145294.5(WDR90):c.1805G>A (p.Arg602Gln)	WDR90 (R602Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2596328	NM_145294.5(WDR90):c.3206C>T (p.Ser1069Leu)	WDR90 (S1069L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595238	NM_145294.5(WDR90):c.5209C>G (p.Arg1737Gly)	WDR90 (R1737G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594924	NM_145294.5(WDR90):c.5059G>A (p.Gly1687Arg)	WDR90 (G1687R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588495	NM_145294.5(WDR90):c.2438G>A (p.Cys813Tyr)	WDR90 (C813Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2567525	NM_145294.5(WDR90):c.2465G>A (p.Arg822Gln)	WDR90 (R822Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559049	NM_145294.5(WDR90):c.2761C>T (p.Arg921Trp)	WDR90 (R921W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555644	NM_145294.5(WDR90):c.3032C>T (p.Ala1011Val)	WDR90 (A1011V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554367	NM_145294.5(WDR90):c.1363G>T (p.Val455Phe)	WDR90 (V455F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554125	NM_145294.5(WDR90):c.1489G>A (p.Val497Ile)	WDR90 (V497I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2553515	NM_145294.5(WDR90):c.1777C>G (p.Arg593Gly)	WDR90 (R593G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549474	NM_145294.5(WDR90):c.3739C>T (p.Arg1247Cys)	WDR90 (R1247C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549107	NM_145294.5(WDR90):c.2165G>A (p.Arg722His)	WDR90 (R722H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2542469	NM_145294.5(WDR90):c.4247C>T (p.Thr1416Met)	WDR90 (T1416M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540769	NM_145294.5(WDR90):c.233C>T (p.Pro78Leu)	WDR90 (P78L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537947	NM_145294.5(WDR90):c.415G>T (p.Ala139Ser)	WDR90 (A139S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529107	NM_145294.5(WDR90):c.272C>T (p.Ser91Phe)	WDR90 (S91F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525954	NM_145294.5(WDR90):c.2747C>T (p.Ser916Leu)	WDR90 (S916L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523825	NM_145294.5(WDR90):c.3364G>T (p.Ala1122Ser)	WDR90 (A1122S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522733	NM_145294.5(WDR90):c.2500G>A (p.Ala834Thr)	WDR90 (A834T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522422	NM_145294.5(WDR90):c.3932C>G (p.Pro1311Arg)	WDR90 (P1311R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520933	NM_145294.5(WDR90):c.2755A>G (p.Ile919Val)	WDR90 (I919V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2520560	NM_145294.5(WDR90):c.2290G>A (p.Gly764Arg)	WDR90 (G764R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520127	NM_145294.5(WDR90):c.5029T>G (p.Phe1677Val)	WDR90 (F1677V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515523	NM_145294.5(WDR90):c.3068C>T (p.Pro1023Leu)	WDR90 (P1023L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513064	NM_145294.5(WDR90):c.4780G>A (p.Ala1594Thr)	WDR90 (A1594T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511391	NM_145294.5(WDR90):c.1436C>T (p.Thr479Met)	WDR90 (T479M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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