ClinVar for Gene (Select 7757) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3335135	NM_007153.3(ZNF208):c.2942G>T (p.Gly981Val)	ZNF208 (G981V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335134	NM_007153.3(ZNF208):c.617G>A (p.Gly206Asp)	ZNF208 (G206D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335133	NM_007153.3(ZNF208):c.616G>A (p.Gly206Ser)	ZNF208 (G206S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335132	NM_007153.3(ZNF208):c.2041A>G (p.Thr681Ala)	ZNF208 (T681A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335131	NM_007153.3(ZNF208):c.3604T>A (p.Cys1202Ser)	ZNF208 (C1202S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335130	NM_007153.3(ZNF208):c.3033C>G (p.Asn1011Lys)	ZNF208 (N1011K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335129	NM_007153.3(ZNF208):c.2261G>C (p.Cys754Ser)	ZNF208 (C754S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335128	NM_007153.3(ZNF208):c.610G>A (p.Glu204Lys)	ZNF208 (E204K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335127	NM_007153.3(ZNF208):c.1157A>T (p.Tyr386Phe)	ZNF208 (Y386F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335126	NM_007153.3(ZNF208):c.2138G>C (p.Arg713Thr)	ZNF208 (R713T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335125	NM_007153.3(ZNF208):c.1267A>G (p.Lys423Glu)	ZNF208 (K423E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335124	NM_007153.3(ZNF208):c.1640A>G (p.His547Arg)	ZNF208 (H547R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335123	NM_007153.3(ZNF208):c.3560A>G (p.His1187Arg)	ZNF208 (H1187R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335122	NM_007153.3(ZNF208):c.2966C>G (p.Thr989Ser)	ZNF208 (T989S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335121	NM_007153.3(ZNF208):c.1013A>G (p.Glu338Gly)	ZNF208 (E338G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335120	NM_007153.3(ZNF208):c.2188T>G (p.Phe730Val)	ZNF208 (F730V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335119	NM_007153.3(ZNF208):c.319G>A (p.Gly107Arg)	ZNF208 (G107R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335118	NM_007153.3(ZNF208):c.3158G>C (p.Gly1053Ala)	ZNF208 (G1053A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335117	NM_007153.3(ZNF208):c.2756G>A (p.Cys919Tyr)	ZNF208 (C919Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335116	NM_007153.3(ZNF208):c.2098A>G (p.Lys700Glu)	ZNF208 (K700E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335115	NM_007153.3(ZNF208):c.1775A>G (p.Gln592Arg)	ZNF208 (Q592R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335114	NM_007153.3(ZNF208):c.3639A>T (p.Arg1213Ser)	ZNF208 (R1213S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194361	NM_007153.3(ZNF208):c.902C>A (p.Thr301Asn)	ZNF208 (T301N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194360	NM_007153.3(ZNF208):c.763A>G (p.Lys255Glu)	ZNF208 (K255E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194358	NM_007153.3(ZNF208):c.599C>T (p.Ser200Phe)	ZNF208 (S200F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194357	NM_007153.3(ZNF208):c.439C>T (p.Arg147Cys)	ZNF208 (R147C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194356	NM_007153.3(ZNF208):c.3662G>T (p.Gly1221Val)	ZNF208 (G1221V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194355	NM_007153.3(ZNF208):c.3647A>G (p.Lys1216Arg)	ZNF208 (K1216R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194354	NM_007153.3(ZNF208):c.3601G>A (p.Glu1201Lys)	ZNF208 (E1201K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194353	NM_007153.3(ZNF208):c.307T>C (p.Tyr103His)	ZNF208 (Y103H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3194352	NM_007153.3(ZNF208):c.2936G>A (p.Gly979Asp)	ZNF208 (G979D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194351	NM_007153.3(ZNF208):c.2656G>A (p.Glu886Lys)	ZNF208 (E886K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194350	NM_007153.3(ZNF208):c.2567C>T (p.Thr856Ile)	ZNF208 (T856I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194349	NM_007153.3(ZNF208):c.2515G>T (p.Gly839Cys)	ZNF208 (G839C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194348	NM_007153.3(ZNF208):c.2479C>G (p.His827Asp)	ZNF208 (H827D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194347	NM_007153.3(ZNF208):c.2458C>T (p.Leu820Phe)	ZNF208 (L820F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194346	NM_007153.3(ZNF208):c.2401G>T (p.Asp801Tyr)	ZNF208 (D801Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194344	NM_007153.3(ZNF208):c.2384A>G (p.His795Arg)	ZNF208 (H795R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194343	NM_007153.3(ZNF208):c.2268A>T (p.Lys756Asn)	ZNF208 (K756N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194342	NM_007153.3(ZNF208):c.2255A>G (p.Glu752Gly)	ZNF208 (E752G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194341	NM_007153.3(ZNF208):c.2144A>G (p.His715Arg)	ZNF208 (H715R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194340	NM_007153.3(ZNF208):c.2102C>G (p.Ala701Gly)	ZNF208 (A701G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194338	NM_007153.3(ZNF208):c.2057T>C (p.Ile686Thr)	ZNF208 (I686T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194337	NM_007153.3(ZNF208):c.1924T>A (p.Cys642Ser)	ZNF208 (C642S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194336	NM_007153.3(ZNF208):c.169G>A (p.Glu57Lys)	ZNF208 (E57K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194335	NM_007153.3(ZNF208):c.1544A>G (p.His515Arg)	ZNF208 (H515R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194334	NM_007153.3(ZNF208):c.1292G>T (p.Gly431Val)	ZNF208 (G431V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194333	NM_007153.3(ZNF208):c.1247A>C (p.Glu416Ala)	ZNF208 (E416A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2681660	NM_007153.3(ZNF208):c.853A>T (p.Asn285Tyr)	ZNF208 (N285Y)	Single nucleotide variant (missense variant +1 more)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2649640	NM_007153.3(ZNF208):c.1062A>C (p.Ser354=)	ZNF208	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2649639	NM_007153.3(ZNF208):c.1533C>T (p.Asn511=)	ZNF208	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2649638	NM_007153.3(ZNF208):c.1557T>C (p.His519=)	ZNF208	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2649637	NM_007153.3(ZNF208):c.1674T>C (p.Cys558=)	ZNF208	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2649636	NM_007153.3(ZNF208):c.2922A>G (p.Lys974=)	ZNF208	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2649635	NM_007153.3(ZNF208):c.3555A>T (p.Ala1185=)	ZNF208	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2623563	NM_007153.3(ZNF208):c.487C>T (p.His163Tyr)	ZNF208 (H163Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620675	NM_007153.3(ZNF208):c.877G>A (p.Ala293Thr)	ZNF208 (A293T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619496	NM_007153.3(ZNF208):c.3650A>T (p.Lys1217Ile)	ZNF208 (K1217I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619313	NM_007153.3(ZNF208):c.2798G>A (p.Ser933Asn)	ZNF208 (S933N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2618323	NM_007153.3(ZNF208):c.3288G>C (p.Trp1096Cys)	ZNF208 (W1096C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2610878	NM_007153.3(ZNF208):c.1073A>G (p.Lys358Arg)	ZNF208 (K358R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2604130	NM_007153.3(ZNF208):c.430G>T (p.Val144Leu)	ZNF208 (V144L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2599111	NM_007153.3(ZNF208):c.1712A>G (p.His571Arg)	ZNF208 (H571R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2599110	NM_007153.3(ZNF208):c.1262G>C (p.Gly421Ala)	ZNF208 (G421A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2589706	NM_007153.3(ZNF208):c.1496G>A (p.Cys499Tyr)	ZNF208 (C499Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2589703	NM_007153.3(ZNF208):c.1982G>C (p.Gly661Ala)	ZNF208 (G661A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2569183	NM_007153.3(ZNF208):c.961G>A (p.Ala321Thr)	ZNF208 (A321T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2556710	NM_007153.3(ZNF208):c.928G>C (p.Glu310Gln)	ZNF208 (E310Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2551359	NM_007153.3(ZNF208):c.780A>C (p.Glu260Asp)	ZNF208 (E260D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540040	NM_007153.3(ZNF208):c.1121G>A (p.Cys374Tyr)	ZNF208 (C374Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2539306	NM_007153.3(ZNF208):c.2804A>G (p.His935Arg)	ZNF208 (H935R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2538940	NM_007153.3(ZNF208):c.2602A>G (p.Lys868Glu)	ZNF208 (K868E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2537076	NM_007153.3(ZNF208):c.2633A>G (p.Tyr878Cys)	ZNF208 (Y878C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526710	NM_007153.3(ZNF208):c.2091A>C (p.Glu697Asp)	ZNF208 (E697D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2525100	NM_007153.3(ZNF208):c.3476A>G (p.His1159Arg)	ZNF208 (H1159R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2519749	NM_007153.3(ZNF208):c.2984A>G (p.His995Arg)	ZNF208 (H995R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2518938	NM_007153.3(ZNF208):c.3233C>T (p.Thr1078Ile)	ZNF208 (T1078I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517007	NM_007153.3(ZNF208):c.2654G>T (p.Gly885Val)	ZNF208 (G885V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2514152	NM_007153.3(ZNF208):c.3322A>G (p.Thr1108Ala)	ZNF208 (T1108A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489000	NM_007153.3(ZNF208):c.3524G>A (p.Gly1175Asp)	ZNF208 (G1175D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2485976	NM_007153.3(ZNF208):c.2971C>A (p.His991Asn)	ZNF208 (H991N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2482321	NM_007153.3(ZNF208):c.189G>T (p.Trp63Cys)	ZNF208 (W63C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2479610	NM_007153.3(ZNF208):c.2821G>A (p.Gly941Arg)	ZNF208 (G941R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2478621	NM_007153.3(ZNF208):c.32T>C (p.Ile11Thr)	ZNF208 (I11T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2476133	NM_007153.3(ZNF208):c.808G>T (p.Ala270Ser)	ZNF208 (A270S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2472031	NM_007153.3(ZNF208):c.2852G>A (p.Gly951Asp)	ZNF208 (G951D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2470829	NM_007153.3(ZNF208):c.2326C>T (p.Pro776Ser)	ZNF208 (P776S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2470311	NM_007153.3(ZNF208):c.550A>C (p.Met184Leu)	ZNF208 (M184L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2466371	NM_007153.3(ZNF208):c.3715A>G (p.Ile1239Val)	ZNF208 (I1239V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2462683	NM_007153.3(ZNF208):c.2398A>G (p.Thr800Ala)	ZNF208 (T800A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2412132	NM_007153.3(ZNF208):c.2395C>T (p.His799Tyr)	ZNF208 (H799Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2401715	NM_007153.3(ZNF208):c.1531A>C (p.Asn511His)	ZNF208 (N511H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398514	NM_007153.3(ZNF208):c.2341G>C (p.Glu781Gln)	ZNF208 (E781Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2396901	NM_007153.3(ZNF208):c.1750G>A (p.Glu584Lys)	ZNF208 (E584K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2373861	NM_007153.3(ZNF208):c.2383C>T (p.His795Tyr)	ZNF208 (H795Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2362420	NM_007153.3(ZNF208):c.1270C>A (p.Pro424Thr)	ZNF208 (P424T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2356063	NM_007153.3(ZNF208):c.2028G>C (p.Lys676Asn)	ZNF208 (K676N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2340613	NM_007153.3(ZNF208):c.1026A>T (p.Lys342Asn)	ZNF208 (K342N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2338218	NM_007153.3(ZNF208):c.3397G>C (p.Val1133Leu)	ZNF208 (V1133L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337693	NM_007153.3(ZNF208):c.2557G>A (p.Val853Ile)	ZNF208 (V853I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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