ZNF208[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 144406	GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	ABHD8, ACP5 +2135 more	Copy number gain	See cases	GPathogenic
Select item 59114	GRCh38/hg38 19p13.12-q11(chr19:13974677-27839676)x3	ABHD8, ADGRE2 +695 more	Copy number gain	See cases	GPathogenic
Select item 147522	GRCh38/hg38 19p13.12-12(chr19:15133594-24193591)x3	ABHD8, AKAP8 +574 more	Copy number gain	See cases	GPathogenic
Select item 57042	GRCh38/hg38 19p13.11-q13.11(chr19:17176767-34924150)x3	LOC130064154, LOC130064155 +625 more	Copy number gain	See cases	GPathogenic
Select item 153725	GRCh38/hg38 19p12(chr19:20637987-21976216)x3	LINC00664, LOC105372321 +27 more	Copy number gain	See cases	GUncertain significance
Select item 146475	GRCh38/hg38 19p12(chr19:21591877-22802732)x3	ZNF100, LINC01233 +13 more	Copy number gain	See cases	GUncertain significance
Select item 145763	GRCh38/hg38 19p12(chr19:21591877-22830542)x3	LINC01233, LINC01785 +14 more	Copy number gain	See cases	GBenign
Select item 145093	GRCh38/hg38 19p12(chr19:21591877-22802673)x3	LINC01233, LINC01785 +13 more	Copy number gain	See cases	GBenign
Select item 805976	NM_007153.3(ZNF208):c.3843G>C (p.Ter1281Tyr)	ZNF208	Single nucleotide variant (stop lost +1 more)	CIC-rearranged sarcoma	Gnot provided
Select item 2307700	NM_007153.3(ZNF208):c.3757T>C (p.Tyr1253His)	ZNF208 (Y1253H)	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 2314588	NM_007153.3(ZNF208):c.3701T>A (p.Phe1234Tyr)	ZNF208 (F1234Y)	Single nucleotide variant (intron 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 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 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 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 2331047	NM_007153.3(ZNF208):c.3614C>T (p.Ala1205Val)	ZNF208 (A1205V)	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 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 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 2649635	NM_007153.3(ZNF208):c.3555A>T (p.Ala1185=)	ZNF208	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2204704	NM_007153.3(ZNF208):c.3547A>G (p.Ile1183Val)	ZNF208 (I1183V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2302584	NM_007153.3(ZNF208):c.3539T>G (p.Met1180Arg)	ZNF208 (M1180R)	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 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 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 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 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 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 2204886	NM_007153.3(ZNF208):c.3193G>A (p.Ala1065Thr)	ZNF208 (A1065T)	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 2287646	NM_007153.3(ZNF208):c.3139C>A (p.His1047Asn)	ZNF208 (H1047N)	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 2308194	NM_007153.3(ZNF208):c.3011A>G (p.Glu1004Gly)	ZNF208 (E1004G)	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 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 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 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 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 2315806	NM_007153.3(ZNF208):c.2924A>G (p.Tyr975Cys)	ZNF208 (Y975C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
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 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 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 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 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 2250372	NM_007153.3(ZNF208):c.2773G>A (p.Ala925Thr)	ZNF208 (A925T)	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 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 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 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 2229990	NM_007153.3(ZNF208):c.2630G>A (p.Ser877Asn)	ZNF208 (S877N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2218206	NM_007153.3(ZNF208):c.2608T>G (p.Tyr870Asp)	ZNF208 (Y870D)	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 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 2337693	NM_007153.3(ZNF208):c.2557G>A (p.Val853Ile)	ZNF208 (V853I)	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 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 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 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 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 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 2309515	NM_007153.3(ZNF208):c.2287A>G (p.Thr763Ala)	ZNF208 (T763A)	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 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 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 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 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 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 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 2252497	NM_007153.3(ZNF208):c.2101G>C (p.Ala701Pro)	ZNF208 (A701P)	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 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 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 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 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 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 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 2255230	NM_007153.3(ZNF208):c.1915T>A (p.Cys639Ser)	ZNF208 (C639S)	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 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 2298211	NM_007153.3(ZNF208):c.1724A>T (p.His575Leu)	ZNF208 (H575L)	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 2212381	NM_007153.3(ZNF208):c.1681G>A (p.Ala561Thr)	ZNF208 (A561T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2303726	NM_007153.3(ZNF208):c.1676G>C (p.Gly559Ala)	ZNF208 (G559A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
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 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 2649638	NM_007153.3(ZNF208):c.1557T>C (p.His519=)	ZNF208	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
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 2649639	NM_007153.3(ZNF208):c.1533C>T (p.Asn511=)	ZNF208	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
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 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 2237079	NM_007153.3(ZNF208):c.1483A>G (p.Lys495Glu)	ZNF208 (K495E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2256530	NM_007153.3(ZNF208):c.1399A>C (p.Ile467Leu)	ZNF208 (I467L)	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 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 3335125	NM_007153.3(ZNF208):c.1267A>G (p.Lys423Glu)	ZNF208 (K423E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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