ClinVar for Gene (Select 10168) - ClinVar

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Links from Gene

Items: 68

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 3335096	NM_006991.5(ZNF197):c.2924T>C (p.Val975Ala)	ZKSCAN7-AS1, ZNF197 +1 more (V762A +2 more)	Single nucleotide variant (missense variant +2 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 3335094	NM_006991.5(ZNF197):c.2585T>C (p.Ile862Thr)	ZKSCAN7-AS1, ZNF197 +1 more (I649T +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 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 3335091	NM_006991.5(ZNF197):c.2063G>A (p.Gly688Asp)	ZKSCAN7-AS1, ZNF197 +1 more (G485D +2 more)	Single nucleotide variant (missense variant +2 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 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 3335088	NM_006991.5(ZNF197):c.2438C>T (p.Thr813Met)	ZKSCAN7-AS1, ZNF197 +1 more (T813M +2 more)	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 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 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 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 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 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 3194280	NM_006991.5(ZNF197):c.3039C>A (p.Phe1013Leu)	ZKSCAN7-AS1, ZNF197 +1 more (F810L +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3194279	NM_006991.5(ZNF197):c.3016A>C (p.Lys1006Gln)	ZKSCAN7-AS1, ZNF197 +1 more (K793Q +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3194278	NM_006991.5(ZNF197):c.2936T>G (p.Ile979Ser)	ZKSCAN7-AS1, ZNF197 +1 more (I776S +2 more)	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 3194276	NM_006991.5(ZNF197):c.2804G>A (p.Cys935Tyr)	ZKSCAN7-AS1, ZNF197 +1 more (C722Y +2 more)	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 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 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 3194272	NM_006991.5(ZNF197):c.2240C>T (p.Ser747Leu)	ZKSCAN7-AS1, ZNF197 +1 more (S534L +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3194271	NM_006991.5(ZNF197):c.2230A>G (p.Ser744Gly)	ZKSCAN7-AS1, ZNF197 +1 more (S744G +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3194270	NM_006991.5(ZNF197):c.2151G>A (p.Met717Ile)	ZKSCAN7-AS1, ZNF197 +1 more (M504I +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 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 2685915	GRCh37/hg19 3p21.31(chr3:44563378-45177006)x3	CDCP1, CLEC3B +12 more	Copy number gain	not provided	GUncertain significance
Select item 2621672	NM_006991.5(ZNF197):c.2623G>A (p.Glu875Lys)	ZKSCAN7-AS1, ZNF197 +1 more (E662K +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 2601632	NM_006991.5(ZNF197):c.3050A>G (p.Gln1017Arg)	ZKSCAN7-AS1, ZNF197 +1 more (Q1017R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2560313	NM_006991.5(ZNF197):c.2480T>G (p.Phe827Cys)	ZKSCAN7-AS1, ZNF197 +1 more (F614C +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2559347	NM_006991.5(ZNF197):c.2580C>G (p.Asn860Lys)	ZKSCAN7-AS1, ZNF197 +1 more (N647K +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
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 2535479	NM_006991.5(ZNF197):c.2758C>G (p.His920Asp)	ZKSCAN7-AS1, ZNF197 +1 more (H717D +2 more)	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 2529922	NM_006991.5(ZNF197):c.2482A>C (p.Ser828Arg)	ZKSCAN7-AS1, ZNF197 +1 more (S625R +2 more)	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 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 2517729	NM_006991.5(ZNF197):c.2128G>A (p.Glu710Lys)	ZKSCAN7-AS1, ZNF197 +1 more (E507K +2 more)	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 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 2464004	NM_006991.5(ZNF197):c.2540C>T (p.Ala847Val)	ZKSCAN7-AS1, ZNF197 +1 more (A847V +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2459954	NM_006991.5(ZNF197):c.1964G>A (p.Cys655Tyr)	ZKSCAN7-AS1, ZNF197 +1 more (C442Y +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 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 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 2387808	NM_006991.5(ZNF197):c.2882A>G (p.Asn961Ser)	ZKSCAN7-AS1, ZNF197 +1 more (N961S +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 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 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 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 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
Select item 2341476	NM_006991.5(ZNF197):c.2257C>T (p.Arg753Trp)	ZKSCAN7-AS1, ZNF197 +1 more (R540W +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 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 2287514	NM_006991.5(ZNF197):c.2305A>G (p.Arg769Gly)	ZKSCAN7-AS1, ZNF197 +1 more (R769G +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 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 2218945	NM_006991.5(ZNF197):c.2545A>G (p.Ser849Gly)	ZKSCAN7-AS1, ZNF197 +1 more (S636G +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2210334	NM_006991.5(ZNF197):c.2207G>C (p.Cys736Ser)	ZKSCAN7-AS1, ZNF197 +1 more (C533S +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 814439	GRCh37/hg19 3p21.31(chr3:44444902-45413927)x1	CDCP1, CLEC3B +16 more	Copy number loss	not provided	GUncertain significance
Select item 562760	GRCh37/hg19 3p24.3-21.31(chr3:16923595-45249923)x2,3	ABHD5, ACAA1 +135 more	Copy number gain	not provided	GPathogenic
Select item 442401	GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3	A4GNT, AADAC +1054 more	Copy number gain	See cases	GPathogenic
Select item 442400	GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)	CMTM6, CMTM7 +1054 more	Copy number gain	See cases	GPathogenic
Select item 253356	GRCh37/hg19 3p22.2-21.31(chr3:37028313-49929220)x3	ABHD5, ACAA1 +177 more	Copy number gain	See cases	GLikely pathogenic

ClinVar

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Links from Gene

Items: 68