ZKSCAN7-AS1[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3193688	NM_001288590.2(ZKSCAN7):c.349C>T (p.His117Tyr)	ZKSCAN7, ZKSCAN7-AS1 (H117Y)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3193689	NM_001288590.2(ZKSCAN7):c.527C>G (p.Ala176Gly)	ZKSCAN7, ZKSCAN7-AS1 (A26G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218447	NM_001288590.2(ZKSCAN7):c.667C>T (p.Arg223Trp)	ZKSCAN7, ZKSCAN7-AS1 (R73W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285991	NM_001288590.2(ZKSCAN7):c.679C>T (p.Pro227Ser)	ZKSCAN7, ZKSCAN7-AS1 (P227S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246361	NM_001288590.2(ZKSCAN7):c.689C>T (p.Thr230Ile)	ZKSCAN7, ZKSCAN7-AS1 (T230I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457504	NM_001288590.2(ZKSCAN7):c.694G>A (p.Ala232Thr)	ZKSCAN7, ZKSCAN7-AS1 (A232T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385170	NM_001288590.2(ZKSCAN7):c.713T>A (p.Val238Glu)	ZKSCAN7, ZKSCAN7-AS1 (V88E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3334769	NM_001288590.2(ZKSCAN7):c.739A>G (p.Ser247Gly)	ZKSCAN7, ZKSCAN7-AS1 (S247G +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3334773	NM_001288590.2(ZKSCAN7):c.745A>G (p.Thr249Ala)	ZKSCAN7, ZKSCAN7-AS1 (T99A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2266482	NM_001288590.2(ZKSCAN7):c.757A>G (p.Arg253Gly)	ZKSCAN7, ZKSCAN7-AS1 (R103G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289295	NM_001288590.2(ZKSCAN7):c.908G>A (p.Gly303Glu)	ZKSCAN7, ZKSCAN7-AS1 (G303E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334768	NM_001288590.2(ZKSCAN7):c.940G>A (p.Val314Ile)	ZKSCAN7, ZKSCAN7-AS1 (V314I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2247408	NM_001288590.2(ZKSCAN7):c.956T>C (p.Phe319Ser)	ZKSCAN7, ZKSCAN7-AS1 (F168S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3193690	NM_001288590.2(ZKSCAN7):c.977C>G (p.Thr326Ser)	ZKSCAN7, ZKSCAN7-AS1 (T326S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193691	NM_001288590.2(ZKSCAN7):c.992G>A (p.Gly331Glu)	ZKSCAN7, ZKSCAN7-AS1 (G180E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334774	NM_001288590.2(ZKSCAN7):c.1065C>G (p.Asp355Glu)	ZKSCAN7, ZKSCAN7-AS1 (D204E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3334775	NM_001288590.2(ZKSCAN7):c.1066A>G (p.Lys356Glu)	ZKSCAN7, ZKSCAN7-AS1 (K205E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2491731	NM_001288590.2(ZKSCAN7):c.1114G>A (p.Glu372Lys)	ZKSCAN7, ZKSCAN7-AS1 (E372K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398857	NM_001288590.2(ZKSCAN7):c.1166G>T (p.Gly389Val)	ZKSCAN7, ZKSCAN7-AS1 (G238V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2246965	NM_001288590.2(ZKSCAN7):c.1191C>A (p.His397Gln)	ZKSCAN7, ZKSCAN7-AS1 (H246Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193681	NM_001288590.2(ZKSCAN7):c.1268C>T (p.Thr423Ile)	ZKSCAN7, ZKSCAN7-AS1 (T272I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2324714	NM_001288590.2(ZKSCAN7):c.1282G>A (p.Val428Ile)	ZKSCAN7, ZKSCAN7-AS1 (V277I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193682	NM_001288590.2(ZKSCAN7):c.1340C>T (p.Ala447Val)	ZKSCAN7, ZKSCAN7-AS1 (A296V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334771	NM_001288590.2(ZKSCAN7):c.1376G>A (p.Arg459Lys)	ZKSCAN7, ZKSCAN7-AS1 (R308K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193683	NM_001288590.2(ZKSCAN7):c.1388G>A (p.Gly463Glu)	ZKSCAN7, ZKSCAN7-AS1 (G463E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2529173	NM_001288590.2(ZKSCAN7):c.1400A>T (p.Tyr467Phe)	ZKSCAN7, ZKSCAN7-AS1 (Y467F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2531147	NM_001288590.2(ZKSCAN7):c.1420A>G (p.Lys474Glu)	ZKSCAN7, ZKSCAN7-AS1 (K323E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193685	NM_001288590.2(ZKSCAN7):c.1499G>A (p.Cys500Tyr)	ZKSCAN7, ZKSCAN7-AS1 (C349Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597540	NM_001288590.2(ZKSCAN7):c.1555G>C (p.Gly519Arg)	ZKSCAN7, ZKSCAN7-AS1 (G519R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329532	NM_001288590.2(ZKSCAN7):c.1591G>T (p.Ala531Ser)	ZKSCAN7, ZKSCAN7-AS1 (A531S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334772	NM_001288590.2(ZKSCAN7):c.1618G>T (p.Asp540Tyr)	ZKSCAN7, ZKSCAN7-AS1 (D540Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2372816	NM_001288590.2(ZKSCAN7):c.1684C>T (p.Arg562Trp)	ZKSCAN7, ZKSCAN7-AS1 (R562W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3193686	NM_001288590.2(ZKSCAN7):c.1685G>A (p.Arg562Gln)	ZKSCAN7, ZKSCAN7-AS1 (R562Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334765	NM_001288590.2(ZKSCAN7):c.1742G>A (p.Cys581Tyr)	ZKSCAN7-AS1, ZKSCAN7 (C581Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334777	NM_001288590.2(ZKSCAN7):c.1796G>T (p.Arg599Leu)	ZKSCAN7, ZKSCAN7-AS1 (R599L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2653724	NM_001288590.2(ZKSCAN7):c.1821T>C (p.Phe607=)	ZKSCAN7, ZKSCAN7-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2473954	NM_001288590.2(ZKSCAN7):c.2081A>G (p.Asn694Ser)	ZKSCAN7, ZKSCAN7-AS1 (N694S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366221	NM_001288590.2(ZKSCAN7):c.2082T>G (p.Asn694Lys)	ZKSCAN7, ZKSCAN7-AS1 (N694K)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2484284	NM_001288590.2(ZKSCAN7):c.2162G>A (p.Cys721Tyr)	ZKSCAN7, ZKSCAN7-AS1 (C721Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3334767	NM_001288590.2(ZKSCAN7):c.2191C>T (p.Arg731Cys)	ZKSCAN7-AS1, ZKSCAN7 (R731C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2592304	NM_001288590.2(ZKSCAN7):c.2243G>T (p.Gly748Val)	ZKSCAN7, ZKSCAN7-AS1 (G748V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197547	NM_173658.4(ZNF660):c.99G>T (p.Gln33His)	ZKSCAN7-AS1, ZNF660 +1 more (Q33H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619719	NM_173658.4(ZNF660):c.127G>C (p.Val43Leu)	ZKSCAN7-AS1, ZNF660 +1 more (V43L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197540	NM_173658.4(ZNF660):c.209G>A (p.Arg70Gln)	ZKSCAN7-AS1, ZNF660 +1 more (R70Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386390	NM_173658.4(ZNF660):c.328G>C (p.Glu110Gln)	ZKSCAN7-AS1, ZNF660 +1 more (E110Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2602889	NM_173658.4(ZNF660):c.367C>T (p.Arg123Trp)	ZKSCAN7-AS1, ZNF660 +1 more (R123W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2372284	NM_173658.4(ZNF660):c.434G>A (p.Arg145Gln)	ZKSCAN7-AS1, ZNF660 +1 more (R145Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3259086	NM_173658.4(ZNF660):c.469A>G (p.Thr157Ala)	ZKSCAN7-AS1, ZNF660 +1 more (T157A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3259085	NM_173658.4(ZNF660):c.493A>G (p.Ile165Val)	ZKSCAN7-AS1, ZNF660 +1 more (I165V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2361384	NM_173658.4(ZNF660):c.494T>C (p.Ile165Thr)	ZKSCAN7-AS1, ZNF660 +1 more (I165T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197542	NM_173658.4(ZNF660):c.537A>C (p.Gln179His)	ZKSCAN7-AS1, ZNF660 +1 more (Q179H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2262661	NM_173658.4(ZNF660):c.538C>T (p.His180Tyr)	ZKSCAN7-AS1, ZNF660 +1 more (H180Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197543	NM_173658.4(ZNF660):c.583T>C (p.Cys195Arg)	ZKSCAN7-AS1, ZNF660 +1 more (C195R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2476495	NM_173658.4(ZNF660):c.640G>A (p.Gly214Arg)	ZKSCAN7-AS1, ZNF660 +1 more (G214R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2225913	NM_173658.4(ZNF660):c.649C>G (p.Pro217Ala)	ZKSCAN7-AS1, ZNF660 +1 more (P217A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2258027	NM_173658.4(ZNF660):c.662A>C (p.Asp221Ala)	ZKSCAN7-AS1, ZNF660 +1 more (D221A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197544	NM_173658.4(ZNF660):c.664G>A (p.Glu222Lys)	ZKSCAN7-AS1, ZNF660 +1 more (E222K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197545	NM_173658.4(ZNF660):c.681C>A (p.Phe227Leu)	ZKSCAN7-AS1, ZNF660 +1 more (F227L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 156210	NM_173658.4(ZNF660):c.721C>T (p.Arg241Cys)	ZKSCAN7-AS1, ZNF660 +1 more (R241C)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2366702	NM_173658.4(ZNF660):c.722G>A (p.Arg241His)	ZKSCAN7-AS1, ZNF660 +1 more (R241H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2525975	NM_173658.4(ZNF660):c.780C>G (p.Asn260Lys)	ZKSCAN7-AS1, ZNF660 +1 more (N260K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197546	NM_173658.4(ZNF660):c.870T>G (p.Ile290Met)	ZKSCAN7-AS1, ZNF660 +1 more (I290M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3259087	NM_173658.4(ZNF660):c.986A>C (p.Glu329Ala)	ZKSCAN7-AS1, ZNF660 +1 more (E329A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335095	NM_006991.5(ZNF197):c.4A>T (p.Thr2Ser)	ZKSCAN7-AS1, ZNF197 +1 more (T2S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3194275	NM_006991.5(ZNF197):c.22C>T (p.His8Tyr)	ZKSCAN7-AS1, ZNF197 +1 more (H8Y)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2409053	NM_006991.5(ZNF197):c.62A>G (p.Asp21Gly)	ZKSCAN7-AS1, ZNF197 +1 more (D21G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2489454	NM_006991.5(ZNF197):c.152A>G (p.His51Arg)	ZKSCAN7-AS1, ZNF197 +1 more (H51R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2533271	NM_006991.5(ZNF197):c.182G>A (p.Ser61Asn)	ZKSCAN7-AS1, ZNF197 +1 more (S61N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2406766	NM_006991.5(ZNF197):c.184C>T (p.Arg62Trp)	ZKSCAN7-AS1, ZNF197 +1 more (R62W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3194273	NM_006991.5(ZNF197):c.226C>T (p.Arg76Cys)	ZKSCAN7-AS1, ZNF197 +1 more (R76C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3194274	NM_006991.5(ZNF197):c.227G>T (p.Arg76Leu)	ZKSCAN7-AS1, ZNF197 +1 more (R76L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3194277	NM_006991.5(ZNF197):c.280C>G (p.Leu94Val)	ZKSCAN7-AS1, ZNF197 +1 more (L94V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2528760	NM_006991.5(ZNF197):c.296G>A (p.Arg99Gln)	ZKSCAN7-AS1, ZNF197 +1 more (R99Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3194281	NM_006991.5(ZNF197):c.340G>A (p.Val114Met)	ZKSCAN7-AS1, ZNF197 +1 more (V114M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3335087	NM_006991.5(ZNF197):c.478C>T (p.His160Tyr)	ZKSCAN7-AS1, ZNF197 +1 more (H160Y)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3335089	NM_006991.5(ZNF197):c.523G>T (p.Ala175Ser)	ZKSCAN7-AS1, ZNF197 +1 more (A175S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2366326	NM_006991.5(ZNF197):c.658G>A (p.Glu220Lys)	ZKSCAN7-AS1, ZNF197 +1 more (E17K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2481744	NM_006991.5(ZNF197):c.673T>C (p.Cys225Arg)	ZKSCAN7-AS1, ZNF197 +1 more (C225R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194282	NM_006991.5(ZNF197):c.676T>G (p.Phe226Val)	ZKSCAN7-AS1, ZNF197 +1 more (F23V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2255186	NM_006991.5(ZNF197):c.718G>A (p.Ala240Thr)	ZKSCAN7-AS1, ZNF197 +1 more (A240T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194283	NM_006991.5(ZNF197):c.758T>C (p.Val253Ala)	ZKSCAN7-AS1, ZNF197 +1 more (V50A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335090	NM_006991.5(ZNF197):c.787G>A (p.Glu263Lys)	ZKSCAN7-AS1, ZNF197 +1 more (E50K +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3335085	NM_006991.5(ZNF197):c.853A>G (p.Lys285Glu)	ZKSCAN7-AS1, ZNF197 +1 more (K82E +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2308782	NM_006991.5(ZNF197):c.869G>T (p.Ser290Ile)	ZKSCAN7-AS1, ZNF197 +1 more (S290I +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2384923	NM_006991.5(ZNF197):c.902G>T (p.Cys301Phe)	ZKSCAN7-AS1, ZNF197 +1 more (C88F +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3335086	NM_006991.5(ZNF197):c.1001G>A (p.Arg334Lys)	ZKSCAN7-AS1, ZNF197 +1 more (R131K +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3335092	NM_006991.5(ZNF197):c.1007C>T (p.Pro336Leu)	ZKSCAN7-AS1, ZNF197 +1 more (P336L +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2545998	NM_006991.5(ZNF197):c.1129A>G (p.Lys377Glu)	ZKSCAN7-AS1, ZNF197 +1 more (K164E +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2616460	NM_006991.5(ZNF197):c.1137T>G (p.Phe379Leu)	ZKSCAN7-AS1, ZNF197 +1 more (F166L +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3335097	NM_006991.5(ZNF197):c.1207T>C (p.Cys403Arg)	ZKSCAN7-AS1, ZNF197 +1 more (C200R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2365940	NM_006991.5(ZNF197):c.1229G>A (p.Arg410His)	ZKSCAN7-AS1, ZNF197 +1 more (R410H +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3335093	NM_006991.5(ZNF197):c.1421G>A (p.Arg474Lys)	ZKSCAN7-AS1, ZNF197 +1 more (R271K +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2454402	NM_006991.5(ZNF197):c.1423C>T (p.Arg475Cys)	ZKSCAN7-AS1, ZNF197 +1 more (R262C +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2387317	NM_006991.5(ZNF197):c.1499A>C (p.His500Pro)	ZKSCAN7-AS1, ZNF197 +1 more (H500P +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2275808	NM_006991.5(ZNF197):c.1505G>C (p.Arg502Thr)	ZKSCAN7-AS1, ZNF197 +1 more (R289T +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2294867	NM_006991.5(ZNF197):c.1565A>C (p.Lys522Thr)	ZKSCAN7-AS1, ZNF197 +1 more (K522T +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3194268	NM_006991.5(ZNF197):c.1598C>T (p.Ser533Phe)	ZKSCAN7-AS1, ZNF197 +1 more (S533F +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3194269	NM_006991.5(ZNF197):c.1637C>T (p.Thr546Ile)	ZKSCAN7-AS1, ZNF197 +1 more (T343I +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2525562	NM_006991.5(ZNF197):c.1702T>C (p.Cys568Arg)	ZKSCAN7-AS1, ZNF197 +1 more (C355R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2352228	NM_006991.5(ZNF197):c.1730G>A (p.Arg577Gln)	ZKSCAN7-AS1, ZNF197 +1 more (R577Q +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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