WDR33[gene] - ClinVar

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Items: 79

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 153085	GRCh38/hg38 2q14.1-14.3(chr2:115302067-129071130)x1	AMMECR1L, BIN1 +254 more	Copy number loss	See cases	GPathogenic
Select item 60184	GRCh38/hg38 2q14.1-21.3(chr2:118086324-134964738)x1	ACMSD, AMER3 +391 more	Copy number loss	See cases	GPathogenic
Select item 60185	GRCh38/hg38 2q14.3(chr2:121824798-128870804)x1	AMMECR1L, BIN1 +121 more	Copy number loss	See cases	GPathogenic
Select item 60186	GRCh38/hg38 2q14.3(chr2:122324343-128371704)x1	LOC115945190, LOC120961783 +101 more	Copy number loss	See cases	GPathogenic
Select item 148393	GRCh38/hg38 2q14.3-21.1(chr2:122847356-129545581)x1	AMMECR1L, BIN1 +116 more	Copy number loss	See cases	GLikely pathogenic
Select item 146132	GRCh38/hg38 2q14.3(chr2:123169989-128460075)x1	AMMECR1L, BIN1 +100 more	Copy number loss	See cases	GPathogenic
Select item 147544	GRCh38/hg38 2q14.3-22.1(chr2:123445762-140592538)x1	ACMSD, AMER3 +336 more	Copy number loss	See cases	GPathogenic
Select item 1180433	NC_000002.12:g.124348648_129410245del	LOC129934710, LOC129934711 +112 more	Deletion	See cases	Gnot provided
Select item 149324	GRCh38/hg38 2q14.3-21.1(chr2:127063206-130527454)x3	AMMECR1L, BIN1 +125 more	Copy number gain	See cases	GUncertain significance
Select item 2310911	NM_032740.4(SFT2D3):c.5C>T (p.Ala2Val)	WDR33, SFT2D3 (A2V)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2262521	NM_032740.4(SFT2D3):c.26A>T (p.Gln9Leu)	WDR33, SFT2D3 (Q9L)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2373752	NM_032740.4(SFT2D3):c.58C>T (p.Pro20Ser)	LOC129934732, SFT2D3 +1 more (P20S)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2217218	NM_032740.4(SFT2D3):c.67G>A (p.Ala23Thr)	LOC129934732, SFT2D3 +1 more (A23T)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2535178	NM_032740.4(SFT2D3):c.308T>C (p.Leu103Pro)	LOC129934732, SFT2D3 +1 more (L103P)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2348877	NM_032740.4(SFT2D3):c.344G>T (p.Gly115Val)	LOC129934732, SFT2D3 +1 more (G115V)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2257613	NM_032740.4(SFT2D3):c.379C>G (p.Arg127Gly)	LOC129934732, SFT2D3 +1 more (R127G)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2590438	NM_032740.4(SFT2D3):c.415G>A (p.Glu139Lys)	LOC129934732, SFT2D3 +1 more (E139K)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2348591	NM_032740.4(SFT2D3):c.487C>T (p.Leu163Phe)	LOC129934732, SFT2D3 +1 more (L163F)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2381945	NM_032740.4(SFT2D3):c.493A>G (p.Ser165Gly)	LOC129934732, SFT2D3 +1 more (S165G)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2365079	NM_032740.4(SFT2D3):c.506C>G (p.Thr169Arg)	LOC129934732, SFT2D3 +1 more (T169R)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2537398	NM_032740.4(SFT2D3):c.547G>A (p.Ala183Thr)	LOC129934732, SFT2D3 +1 more (A183T)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2274584	NM_032740.4(SFT2D3):c.548C>T (p.Ala183Val)	LOC129934732, SFT2D3 +1 more (A183V)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2482222	NM_032740.4(SFT2D3):c.577G>A (p.Gly193Ser)	LOC129934732, SFT2D3 +1 more (G193S)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2389221	NM_018383.5(WDR33):c.4007G>A (p.Arg1336Gln)	WDR33 (R1336Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2214062	NM_018383.5(WDR33):c.3968C>T (p.Pro1323Leu)	WDR33 (P1323L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2494953	NM_018383.5(WDR33):c.3922C>T (p.Arg1308Trp)	WDR33 (R1308W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2618046	NM_018383.5(WDR33):c.3620A>G (p.Asp1207Gly)	WDR33 (D1207G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2517124	NM_018383.5(WDR33):c.3608A>G (p.His1203Arg)	WDR33 (H1203R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2348960	NM_018383.5(WDR33):c.3526G>A (p.Gly1176Arg)	WDR33 (G1176R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2270354	NM_018383.5(WDR33):c.3514C>T (p.Arg1172Cys)	WDR33 (R1172C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2602716	NM_018383.5(WDR33):c.3476G>A (p.Gly1159Glu)	WDR33 (G1159E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2290466	NM_018383.5(WDR33):c.3437G>A (p.Arg1146Gln)	WDR33 (R1146Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2401740	NM_018383.5(WDR33):c.3344G>A (p.Arg1115His)	WDR33 (R1115H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2458384	NM_018383.5(WDR33):c.3340G>A (p.Gly1114Ser)	WDR33 (G1114S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2517689	NM_018383.5(WDR33):c.3280C>T (p.Pro1094Ser)	WDR33 (P1094S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2460072	NM_018383.5(WDR33):c.3279C>G (p.Asp1093Glu)	WDR33 (D1093E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2475672	NM_018383.5(WDR33):c.3138G>C (p.Arg1046Ser)	WDR33 (R1046S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2409020	NM_018383.5(WDR33):c.3070C>T (p.Arg1024Cys)	WDR33 (R1024C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2344215	NM_018383.5(WDR33):c.3049G>C (p.Asp1017His)	WDR33 (D1017H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2298208	NM_018383.5(WDR33):c.2878C>T (p.Arg960Cys)	WDR33 (R960C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2232326	NM_018383.5(WDR33):c.2718A>C (p.Lys906Asn)	WDR33 (K906N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2353568	NM_018383.5(WDR33):c.2591C>T (p.Pro864Leu)	WDR33 (P864L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2368561	NM_018383.5(WDR33):c.2558G>A (p.Arg853Gln)	WDR33 (R853Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2466680	NM_018383.5(WDR33):c.2486G>A (p.Gly829Asp)	WDR33 (G829D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2237789	NM_018383.5(WDR33):c.2465A>G (p.His822Arg)	WDR33 (H822R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2322777	NM_018383.5(WDR33):c.2456T>C (p.Leu819Pro)	WDR33 (L819P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2271859	NM_018383.5(WDR33):c.2384G>T (p.Gly795Val)	WDR33 (G795V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2457964	NM_018383.5(WDR33):c.2218A>G (p.Met740Val)	WDR33 (M740V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2261793	NM_018383.5(WDR33):c.2131C>T (p.Pro711Ser)	WDR33 (P711S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2491300	NM_018383.5(WDR33):c.2093G>A (p.Ser698Asn)	WDR33 (S698N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2212481	NM_018383.5(WDR33):c.1885C>T (p.Pro629Ser)	WDR33 (P629S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2464935	NM_018383.5(WDR33):c.1883C>T (p.Pro628Leu)	WDR33 (P628L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2338420	NM_018383.5(WDR33):c.1805A>G (p.Gln602Arg)	WDR33 (Q602R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2601399	NM_018383.5(WDR33):c.1750G>A (p.Gly584Arg)	WDR33 (G584R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2372766	NM_018383.5(WDR33):c.1738A>G (p.Thr580Ala)	WDR33 (T580A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2220186	NM_018383.5(WDR33):c.1537G>A (p.Val513Ile)	WDR33, LOC126806344 (V513I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2317568	NM_018383.5(WDR33):c.1505C>T (p.Ala502Val)	WDR33 (A502V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2372857	NM_018383.5(WDR33):c.1449A>C (p.Gln483His)	WDR33 (Q483H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2227198	NM_018383.5(WDR33):c.1293T>G (p.Asp431Glu)	WDR33 (D431E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2247313	NM_018383.5(WDR33):c.1116G>A (p.Met372Ile)	WDR33 (M372I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2398442	NM_018383.5(WDR33):c.244A>G (p.Ile82Val)	WDR33 (I82V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2406507	NM_018383.5(WDR33):c.238C>T (p.Arg80Trp)	WDR33 (R80W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3062651	GRCh37/hg19 2q12.2-21.2(chr2:106755586-134302739)x1	ACOXL, ACTR3 +121 more	Copy number loss	not specified	GPathogenic
Select item 3062624	GRCh37/hg19 2q14.3(chr2:125361063-129616153)x3	AMMECR1L, BIN1 +16 more	Copy number gain	not specified	GUncertain significance
Select item 2684675	GRCh37/hg19 2q14.3(chr2:124806439-128906413)x1	AMMECR1L, BIN1 +15 more	Copy number loss	not provided	GUncertain significance
Select item 2422856	NC_000002.11:g.(?_127806102)_(129076137_?)del	ERCC3, PROC +14 more	Deletion	Thrombophilia due to protein C deficiency, autosomal dominant	GPathogenic
Select item 2422380	NC_000002.11:g.(?_127451420)_(129076137_?)del	POLR2D, PROC +15 more	Deletion	not provided	GPathogenic
Select item 1703543	GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373)	ABCA12, ABCB11 +1216 more	Copy number gain	Mosaic trisomy 2	GPathogenic
Select item 1679114	GRCh37/hg19 2q13-22.3(chr2:112475655-145691999)x3	EPB41L5, ERCC3 +120 more	Copy number gain	2q13q22.3 microduplication syndrome	GPathogenic
Select item 1526896	GRCh37/hg19 2q14.3(chr2:128024782-129332242)	AMMECR1L, ERCC3 +12 more	Copy number gain	not specified	GUncertain significance
Select item 1340017	GRCh37/hg19 2q13-22.3(chr2:111484468-146333604)x3	GPR39, IL1F10 +122 more	Copy number gain	not provided	GPathogenic
Select item 1339988	GRCh37/hg19 2q14.3-22.2(chr2:122699106-143799629)x1	ACMSD, AMER3 +64 more	Copy number loss	not provided	GPathogenic
Select item 929341	GRCh37/hg19 2q14.3-21.2(chr2:122952356-133826358)x1	AMER3, AMMECR1L +44 more	Copy number loss	See cases	GLikely pathogenic
Select item 814303	GRCh37/hg19 2q14.3(chr2:128494642-128910835)x3	WDR33, POLR2D +3 more	Copy number gain	not provided	GUncertain significance
Select item 524189	Single allele	ACMSD, C2orf27A +486 more	Deletion	not provided	GLikely pathogenic
Select item 523163	GRCh37/hg19 2q12.1-24.3(chr2:104172062-168223828)x1	CCDC74B, CCDC93 +218 more	Copy number loss	Poly (ADP-Ribose) polymerase inhibitor response	Gdrug response
Select item 442998	GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)	DCAF17, DCDC2C +1214 more	Copy number gain	See cases	GPathogenic
Select item 442997	GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3	AAK1, AAMP +1214 more	Copy number gain	See cases	GPathogenic
Select item 441676	GRCh37/hg19 2q14.2-22.1(chr2:120571363-141627287)x1	ACMSD, AMER3 +74 more	Copy number loss	See cases	GPathogenic

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Items: 79