ClinVar for Gene (Select 284371) - ClinVar

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Links from Gene

Items: 67

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3198761	NM_001136499.2(ZNF841):c.880T>C (p.Ser294Pro)	ZNF841 (S294P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198760	NM_001136499.2(ZNF841):c.737C>T (p.Ser246Leu)	ZNF841 (S130L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198758	NM_001136499.2(ZNF841):c.2558A>G (p.Glu853Gly)	LOC126862922, ZNF841 (E853G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198757	NM_001136499.2(ZNF841):c.2439G>A (p.Met813Ile)	LOC126862922, ZNF841 (M697I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198756	NM_001136499.2(ZNF841):c.206T>C (p.Val69Ala)	ZNF841 (V69A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3198755	NM_001136499.2(ZNF841):c.1993C>T (p.Arg665Cys)	LOC126862922, ZNF841 (R549C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198754	NM_001136499.2(ZNF841):c.1898T>C (p.Val633Ala)	LOC126862922, ZNF841 (V517A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198753	NM_001136499.2(ZNF841):c.1343A>G (p.Gln448Arg)	ZNF841 (Q332R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198752	NM_001136499.2(ZNF841):c.1334T>G (p.Val445Gly)	ZNF841 (V329G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198750	NM_001136499.2(ZNF841):c.1325C>T (p.Ser442Leu)	ZNF841 (S443L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2684892	GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3	ACP4, ADM5 +261 more	Copy number gain	not provided	GLikely pathogenic
Select item 2615221	NM_001136499.2(ZNF841):c.512G>C (p.Ser171Thr)	ZNF841 (S172T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612598	NM_001136499.2(ZNF841):c.393C>G (p.Phe131Leu)	ZNF841 (F132L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610124	NM_001136499.2(ZNF841):c.1521T>G (p.His507Gln)	ZNF841 (H507Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2561101	NM_001136499.2(ZNF841):c.1528G>A (p.Glu510Lys)	ZNF841 (E511K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552294	NM_001136499.2(ZNF841):c.1394T>C (p.Val465Ala)	ZNF841 (V466A +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2523503	NM_001136499.2(ZNF841):c.1720T>C (p.Cys574Arg)	LOC126862922, ZNF841 (C574R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516616	NM_001136499.2(ZNF841):c.2434C>G (p.Gln812Glu)	LOC126862922, ZNF841 (Q696E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2516601	NM_001136499.2(ZNF841):c.2756C>T (p.Thr919Ile)	LOC126862922, ZNF841 (T803I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2510616	NM_001136499.2(ZNF841):c.1427G>A (p.Arg476Gln)	ZNF841 (R476Q +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2488422	NM_001136499.2(ZNF841):c.851C>T (p.Thr284Ile)	ZNF841 (T168I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470437	NM_001136499.2(ZNF841):c.1850G>A (p.Arg617Gln)	LOC126862922, ZNF841 (R617Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460816	NM_001136499.2(ZNF841):c.1426C>T (p.Arg476Trp)	ZNF841 (R477W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409294	NM_001136499.2(ZNF841):c.2665C>T (p.Arg889Cys)	LOC126862922, ZNF841 (R773C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407742	NM_001136499.2(ZNF841):c.764A>G (p.His255Arg)	ZNF841 (H256R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400179	NM_001136499.2(ZNF841):c.2413C>T (p.Arg805Cys)	LOC126862922, ZNF841 (R805C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2390456	NM_001136499.2(ZNF841):c.1861G>A (p.Gly621Arg)	LOC126862922, ZNF841 (G622R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381622	NM_001136499.2(ZNF841):c.368G>A (p.Ser123Asn)	ZNF841 (S124N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378886	NM_001136499.2(ZNF841):c.1210A>G (p.Asn404Asp)	ZNF841 (N288D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377566	NM_001136499.2(ZNF841):c.523G>A (p.Val175Ile)	ZNF841 (V59I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351639	NM_001136499.2(ZNF841):c.2414G>A (p.Arg805His)	LOC126862922, ZNF841 (R806H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349560	NM_001136499.2(ZNF841):c.827T>C (p.Leu276Pro)	ZNF841 (L276P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340319	NM_001136499.2(ZNF841):c.539T>C (p.Met180Thr)	ZNF841 (M181T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325126	NM_001136499.2(ZNF841):c.7C>G (p.Leu3Val)	ZNF841 (L3V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2315318	NM_001136499.2(ZNF841):c.133G>A (p.Gly45Ser)	ZNF841 (G45S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2304942	NM_001136499.2(ZNF841):c.1517T>C (p.Val506Ala)	ZNF841 (V506A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297880	NM_001136499.2(ZNF841):c.2578C>T (p.Arg860Trp)	LOC126862922, ZNF841 (R744W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295264	NM_001136499.2(ZNF841):c.2419A>G (p.Ile807Val)	LOC126862922, ZNF841 (I691V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2292587	NM_001136499.2(ZNF841):c.896A>G (p.His299Arg)	ZNF841 (H299R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283636	NM_001136499.2(ZNF841):c.1021G>A (p.Gly341Arg)	ZNF841 (G341R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268222	NM_001136499.2(ZNF841):c.2338C>T (p.Leu780Phe)	LOC126862922, ZNF841 (L781F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244091	NM_001136499.2(ZNF841):c.2698G>A (p.Ala900Thr)	LOC126862922, ZNF841 (A901T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2242124	NM_001136499.2(ZNF841):c.1168A>G (p.Thr390Ala)	ZNF841 (T391A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241730	NM_001136499.2(ZNF841):c.796T>A (p.Cys266Ser)	ZNF841 (C266S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224565	NM_001136499.2(ZNF841):c.1339C>T (p.His447Tyr)	ZNF841 (H331Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215042	NM_001136499.2(ZNF841):c.1561G>A (p.Ala521Thr)	ZNF841 (A522T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204091	NM_001136499.2(ZNF841):c.2450G>T (p.Gly817Val)	LOC126862922, ZNF841 (G817V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2204058	NM_001136499.2(ZNF841):c.1820T>C (p.Ile607Thr)	LOC126862922, ZNF841 (I491T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1526670	GRCh37/hg19 19q13.33-13.41(chr19:49911081-53127438)	FPR3, ZNF577 +115 more	Copy number gain	not specified	GLikely pathogenic
Select item 980768	GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3	FLT3LG, FPR1 +308 more	Copy number gain	not provided	GPathogenic
Select item 972980	GRCh37/hg19 19q13.32-13.42(chr19:47939842-54626871)	FUZ, GARIN5A +228 more	Copy number gain	not provided	Gnot provided
Select item 816084	GRCh37/hg19 19q13.31-13.42(chr19:44738088-53621561)x3	CLDND2, IGSF23 +293 more	Copy number gain	not provided	GPathogenic
Select item 443499	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	A1BG, ABCA7 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443498	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	LILRA4, LILRA5 +1364 more	Copy number gain	See cases	GPathogenic
Select item 394342	GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3	A1BG, ACP4 +280 more	Copy number gain	See cases	GPathogenic
Select item 221886	GRCh37/hg19 19q13.41(chr19:52272131-52588718)x3	ZNF613, ZNF614 +8 more	Copy number gain	Premature ovarian failure	GBenign
Select item 157458	NM_001005738.1(FPR2):c.290_344331dup	FPR2, FPR3 +20 more	Duplication	Gestational diabetes mellitus uncontrolled	Gnot provided
Select item 154882	GRCh38/hg38 19q13.41(chr19:51785545-52075049)x3	FPR3, LOC126862921 +16 more	Copy number gain	See cases	GLikely benign
Select item 154637	GRCh38/hg38 19q13.41(chr19:51769103-52124150)x3	FPR2, FPR3 +20 more	Copy number gain	See cases	GBenign
Select item 147613	GRCh38/hg38 19q13.41(chr19:51865544-52113443)x3	LOC126862922, LOC126862923 +16 more	Copy number gain	See cases	GBenign
Select item 146579	GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3	MIR498, MIR512-1 +782 more	Copy number gain	See cases	GPathogenic
Select item 59127	GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3	A1BG, A1BG-AS1 +647 more	Copy number gain	See cases	GPathogenic
Select item 59126	GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3	LOC113939975, LOC116286194 +806 more	Copy number gain	See cases	GPathogenic
Select item 59117	GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3	LOC130064933, LOC130064934 +1093 more	Copy number gain	See cases	GPathogenic
Select item 59116	GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3	ZBTB45, ZFP28 +1081 more	Copy number gain	See cases	GPathogenic
Select item 58803	GRCh38/hg38 19q13.41(chr19:51824349-52113443)x3	FPR3, LOC126862921 +18 more	Copy number gain	See cases	GUncertain significance
Select item 57219	GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3	LOC130065070, LOC130065071 +761 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 67