ClinVar for Gene (Select 83889) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3332997	NM_001291088.2(WDR87):c.1733G>A (p.Cys578Tyr)	WDR87 (C539Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332996	NM_001291088.2(WDR87):c.7212A>T (p.Arg2404Ser)	WDR87 (R2365S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332995	NM_001291088.2(WDR87):c.100T>C (p.Cys34Arg)	WDR87 (C34R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332994	NM_001291088.2(WDR87):c.3044G>C (p.Ser1015Thr)	WDR87 (S1015T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332993	NM_001291088.2(WDR87):c.8666C>T (p.Ala2889Val)	WDR87 (A2889V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332992	NM_001291088.2(WDR87):c.121C>T (p.Arg41Trp)	WDR87 (R41W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332991	NM_001291088.2(WDR87):c.62T>C (p.Ile21Thr)	WDR87 (I21T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332990	NM_001291088.2(WDR87):c.6838G>A (p.Glu2280Lys)	WDR87 (E2280K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332989	NM_001291088.2(WDR87):c.5408C>T (p.Ser1803Phe)	WDR87 (S1764F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332988	NM_001291088.2(WDR87):c.1411C>T (p.Arg471Trp)	WDR87 (R432W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332987	NM_001291088.2(WDR87):c.8722G>A (p.Val2908Ile)	WDR87 (V2869I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3332986	NM_001291088.2(WDR87):c.7055T>C (p.Met2352Thr)	WDR87 (M2313T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3332985	NM_001291088.2(WDR87):c.7972G>C (p.Val2658Leu)	WDR87 (V2619L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332984	NM_001291088.2(WDR87):c.2971A>T (p.Thr991Ser)	WDR87 (T952S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332983	NM_001291088.2(WDR87):c.1252G>A (p.Asp418Asn)	WDR87 (D418N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332982	NM_001291088.2(WDR87):c.5504A>G (p.Glu1835Gly)	WDR87 (E1835G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332981	NM_001291088.2(WDR87):c.7702C>T (p.Arg2568Cys)	WDR87 (R2568C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3332980	NM_001291088.2(WDR87):c.1136G>A (p.Arg379Gln)	WDR87 (R379Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3257422	NM_001291088.2(WDR87):c.1835T>G (p.Phe612Cys)	WDR87 (F573C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3257219	NM_001291088.2(WDR87):c.8279A>G (p.Glu2760Gly)	WDR87 (E2721G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3190354	NM_001291088.2(WDR87):c.1028C>T (p.Ala343Val)	WDR87 (A304V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190353	NM_001291088.2(WDR87):c.949C>A (p.Leu317Met)	WDR87 (L278M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190351	NM_001291088.2(WDR87):c.7846C>T (p.His2616Tyr)	WDR87 (H2577Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190350	NM_001291088.2(WDR87):c.7802T>C (p.Leu2601Ser)	WDR87 (L2601S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190348	NM_001291088.2(WDR87):c.7451C>A (p.Pro2484His)	WDR87 (P2484H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190346	NM_001291088.2(WDR87):c.6778G>C (p.Glu2260Gln)	WDR87 (E2221Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190345	NM_001291088.2(WDR87):c.6665G>A (p.Gly2222Glu)	WDR87 (G2183E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190343	NM_001291088.2(WDR87):c.6011T>C (p.Leu2004Pro)	WDR87 (L2004P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190342	NM_001291088.2(WDR87):c.5888C>G (p.Ala1963Gly)	WDR87 (A1924G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190340	NM_001291088.2(WDR87):c.5673A>C (p.Lys1891Asn)	WDR87 (K1891N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190339	NM_001291088.2(WDR87):c.5529A>C (p.Gln1843His)	WDR87 (Q1804H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190337	NM_001291088.2(WDR87):c.4930G>C (p.Glu1644Gln)	WDR87 (E1605Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190336	NM_001291088.2(WDR87):c.4847T>C (p.Ile1616Thr)	WDR87 (I1616T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190335	NM_001291088.2(WDR87):c.4687G>C (p.Val1563Leu)	WDR87 (V1563L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190334	NM_001291088.2(WDR87):c.4628C>T (p.Ser1543Phe)	WDR87 (S1504F +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190333	NM_001291088.2(WDR87):c.4372G>A (p.Glu1458Lys)	WDR87 (E1419K +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190332	NM_001291088.2(WDR87):c.4341G>T (p.Gln1447His)	WDR87 (Q1408H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190331	NM_001291088.2(WDR87):c.4265T>C (p.Met1422Thr)	WDR87 (M1383T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190330	NM_001291088.2(WDR87):c.4234G>A (p.Val1412Ile)	WDR87 (V1373I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190329	NM_001291088.2(WDR87):c.4229A>C (p.Lys1410Thr)	WDR87 (K1371T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190328	NM_001291088.2(WDR87):c.4175A>G (p.Lys1392Arg)	WDR87 (K1353R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190327	NM_001291088.2(WDR87):c.4058A>G (p.Lys1353Arg)	WDR87 (K1314R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190326	NM_001291088.2(WDR87):c.3780C>G (p.Ile1260Met)	WDR87 (I1221M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190325	NM_001291088.2(WDR87):c.3575T>C (p.Val1192Ala)	WDR87 (V1153A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190324	NM_001291088.2(WDR87):c.2863C>T (p.Pro955Ser)	WDR87 (P916S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190323	NM_001291088.2(WDR87):c.2788G>T (p.Val930Phe)	WDR87 (V930F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190322	NM_001291088.2(WDR87):c.2788G>A (p.Val930Ile)	WDR87 (V891I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190321	NM_001291088.2(WDR87):c.2732G>A (p.Arg911Lys)	WDR87 (R911K +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190320	NM_001291088.2(WDR87):c.2708G>C (p.Gly903Ala)	WDR87 (G903A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190319	NM_001291088.2(WDR87):c.2600G>A (p.Arg867Lys)	WDR87 (R828K +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190318	NM_001291088.2(WDR87):c.1732T>G (p.Cys578Gly)	WDR87 (C578G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190317	NM_001291088.2(WDR87):c.1666A>C (p.Ser556Arg)	WDR87 (S517R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190316	NM_001291088.2(WDR87):c.1646G>A (p.Arg549Gln)	WDR87 (R510Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3190315	NM_001291088.2(WDR87):c.1645C>T (p.Arg549Trp)	WDR87 (R549W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190314	NM_001291088.2(WDR87):c.1318C>T (p.Arg440Cys)	WDR87 (R401C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3190313	NM_001291088.2(WDR87):c.1283C>G (p.Thr428Arg)	WDR87 (T389R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062386	GRCh37/hg19 19q11-13.2(chr19:28271146-41508851)x3	SLC7A9, SNRPA +215 more	Copy number gain	not specified	GPathogenic
Select item 3020582	NM_001291088.2(WDR87):c.8054A>G (p.Tyr2685Cys)	WDR87 (Y2646C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3019869	NM_001291088.2(WDR87):c.1905C>T (p.Phe635=)	WDR87	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3003032	NM_001291088.2(WDR87):c.3074G>A (p.Arg1025Lys)	WDR87 (R986K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2974543	NM_001291088.2(WDR87):c.6669AGA[3] (p.Glu2227del)	WDR87 (E2188del +1 more)	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 2971109	NM_001291088.2(WDR87):c.8341C>T (p.Arg2781Ter)	WDR87 (R2742* +1 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2965131	NM_001291088.2(WDR87):c.7022A>G (p.Lys2341Arg)	WDR87 (K2302R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2964578	NM_001291088.2(WDR87):c.1862T>C (p.Phe621Ser)	WDR87 (F582S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2964222	NM_001291088.2(WDR87):c.5551C>T (p.Leu1851=)	WDR87	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2918016	NM_001291088.2(WDR87):c.1512C>T (p.Gly504=)	WDR87	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2910793	NM_001291088.2(WDR87):c.3726T>C (p.Asn1242=)	WDR87	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2896770	NM_001291088.2(WDR87):c.5215C>A (p.Leu1739Met)	WDR87 (L1700M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2889003	NM_001291088.2(WDR87):c.3607C>A (p.His1203Asn)	WDR87 (H1203N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2888088	NM_001291088.2(WDR87):c.8718C>T (p.His2906=)	WDR87	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2861306	NM_001291088.2(WDR87):c.3126G>A (p.Gln1042=)	WDR87	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2860378	NM_001291088.2(WDR87):c.582del (p.Asp195fs)	WDR87 (D156fs +1 more)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 2858899	NM_001291088.2(WDR87):c.5310A>G (p.Lys1770=)	WDR87	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2853782	NM_001291088.2(WDR87):c.7082_7085del (p.Ser2361fs)	WDR87 (S2322fs +1 more)	Deletion (frameshift variant)	not provided	GBenign
Select item 2853295	NM_001291088.2(WDR87):c.2285G>A (p.Arg762His)	WDR87 (R762H +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2832171	NM_001291088.2(WDR87):c.3158A>T (p.His1053Leu)	WDR87 (H1014L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2808794	NM_001291088.2(WDR87):c.2986A>G (p.Met996Val)	WDR87 (M996V +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2806766	NM_001291088.2(WDR87):c.1755T>C (p.His585=)	WDR87	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2800207	NM_001291088.2(WDR87):c.562C>T (p.His188Tyr)	WDR87 (H149Y +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2768429	NM_001291088.2(WDR87):c.1515T>C (p.Ala505=)	WDR87	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2765838	NM_001291088.2(WDR87):c.7221C>T (p.Ser2407=)	WDR87	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2752052	NM_001291088.2(WDR87):c.4864C>T (p.Arg1622Ter)	WDR87 (R1583* +1 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2748871	NM_001291088.2(WDR87):c.4478C>T (p.Thr1493Ile)	WDR87 (T1493I +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2734996	NM_001291088.2(WDR87):c.6561C>T (p.Asn2187=)	WDR87	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2723140	NM_001291088.2(WDR87):c.1600G>A (p.Val534Met)	WDR87 (V534M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2720238	NM_001291088.2(WDR87):c.2626T>C (p.Tyr876His)	WDR87 (Y876H +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2718567	NM_001291088.2(WDR87):c.4260A>T (p.Val1420=)	WDR87	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2713264	NM_001291088.2(WDR87):c.8521C>T (p.Arg2841Trp)	WDR87 (R2841W +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2711758	NM_001291088.2(WDR87):c.57C>T (p.Asp19=)	WDR87	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2710778	NM_001291088.2(WDR87):c.2787G>A (p.Met929Ile)	WDR87 (M929I +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2708913	NM_001291088.2(WDR87):c.6997AAG[2] (p.Lys2335del)	WDR87 (K2296del +1 more)	Microsatellite (inframe_deletion)	not provided	GUncertain significance
Select item 2695244	NM_001291088.2(WDR87):c.2217C>G (p.Ala739=)	WDR87	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2693824	NM_001291088.2(WDR87):c.7981C>T (p.Gln2661Ter)	WDR87 (Q2622* +1 more)	Single nucleotide variant (nonsense)	not provided	GLikely benign
Select item 2681646	NM_001291088.2(WDR87):c.1164G>T (p.Leu388Phe)	WDR87 (L349F +1 more)	Single nucleotide variant (missense variant)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2649779	NM_001291088.2(WDR87):c.4215T>C (p.Ile1405=)	WDR87	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2649778	NM_001291088.2(WDR87):c.5199C>G (p.Ala1733=)	WDR87	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2624088	NM_001291088.2(WDR87):c.6389C>T (p.Thr2130Ile)	WDR87 (T2091I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623951	NM_001291088.2(WDR87):c.4340A>G (p.Gln1447Arg)	WDR87 (Q1408R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621768	NM_001291088.2(WDR87):c.6503G>A (p.Arg2168Gln)	WDR87 (R2129Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2618702	NM_001291088.2(WDR87):c.8560C>T (p.Pro2854Ser)	WDR87 (P2815S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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