Related gene-specific medical variations for Gene (Select 101929746) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 100 of 178

<< First< Prev

Page of 2

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3011938	NM_001282933.2(ZNF341):c.1881C>T (p.Cys627=)	ZNF341-AS1, ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3004343	NM_001282933.2(ZNF341):c.2202C>T (p.Gly734=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3003947	NM_001282933.2(ZNF341):c.2448G>C (p.Val816=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3002007	NM_001282933.2(ZNF341):c.2145C>G (p.Gly715=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3000444	NM_001282933.2(ZNF341):c.2035+12T>C	ZNF341, ZNF341-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2998067	NM_001282933.2(ZNF341):c.1914G>A (p.Lys638=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2997947	NM_001282933.2(ZNF341):c.2511C>T (p.Ala837=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2994790	NM_001282933.2(ZNF341):c.1853-6C>T	ZNF341, ZNF341-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2993479	NM_001282933.2(ZNF341):c.1964+1G>A	ZNF341, ZNF341-AS1	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 2980003	NM_001282933.2(ZNF341):c.2081G>A (p.Arg694His)	ZNF341, ZNF341-AS1 (R694H +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2972463	NM_001282933.2(ZNF341):c.2252C>T (p.Ala751Val)	ZNF341, ZNF341-AS1 (A744V +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2970364	NM_001282933.2(ZNF341):c.2409C>T (p.Ile803=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2967583	NM_001282933.2(ZNF341):c.2544C>T (p.Val848=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2965818	NM_001282933.2(ZNF341):c.2001G>A (p.Pro667=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2965676	NM_001282933.2(ZNF341):c.2282G>T (p.Arg761Leu)	ZNF341, ZNF341-AS1 (R671L +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2955654	NM_001282933.2(ZNF341):c.2535T>G (p.Ala845=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2908760	NM_001282933.2(ZNF341):c.2430C>T (p.Gly810=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2902000	NM_001282933.2(ZNF341):c.2355C>T (p.Pro785=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2895766	NM_001282933.2(ZNF341):c.2352G>A (p.Val784=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2879958	NM_001282933.2(ZNF341):c.2467G>A (p.Gly823Arg)	ZNF341, ZNF341-AS1 (G733R +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2874561	NM_001282933.2(ZNF341):c.2371A>G (p.Lys791Glu)	ZNF341, ZNF341-AS1 (K701E +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2870424	NM_001282933.2(ZNF341):c.2547C>T (p.Tyr849=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2794092	NM_001282933.2(ZNF341):c.2130G>A (p.Lys710=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2788201	NM_001282933.2(ZNF341):c.2248A>C (p.Arg750=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2776102	NM_001282933.2(ZNF341):c.2241C>G (p.Pro747=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2723579	NM_001282933.2(ZNF341):c.2242C>A (p.Gln748Lys)	ZNF341, ZNF341-AS1 (Q741K +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2718569	NM_001282933.2(ZNF341):c.2262C>A (p.Arg754=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2705623	NM_001282933.2(ZNF341):c.1909C>T (p.Leu637=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2702138	NM_001282933.2(ZNF341):c.1877T>C (p.Val626Ala)	ZNF341, ZNF341-AS1 (V626A +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2628236	NM_001282933.2(ZNF341):c.2036-62G>A	ZNF341, ZNF341-AS1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 2614954	NM_001282933.2(ZNF341):c.2390C>G (p.Pro797Arg)	ZNF341, ZNF341-AS1 (P707R +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2550463	NM_001282933.2(ZNF341):c.2344G>A (p.Gly782Arg)	ZNF341, ZNF341-AS1 (G692R +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2527706	NM_001282933.2(ZNF341):c.1896C>A (p.Asn632Lys)	ZNF341, ZNF341-AS1 (N625K +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2421947	NM_001282933.2(ZNF341):c.2520A>G (p.Pro840=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2416160	NM_001282933.2(ZNF341):c.2519C>T (p.Pro840Leu)	ZNF341, ZNF341-AS1 (P750L +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2378910	NM_001282933.2(ZNF341):c.2269G>C (p.Gly757Arg)	ZNF341, ZNF341-AS1 (G757R +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2297143	NM_001282933.2(ZNF341):c.2197C>A (p.Leu733Ile)	ZNF341, ZNF341-AS1 (L643I +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2285311	NM_001282933.2(ZNF341):c.2197C>T (p.Leu733Phe)	ZNF341-AS1, ZNF341 (L726F +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2256624	NM_001282933.2(ZNF341):c.2489T>C (p.Leu830Pro)	ZNF341-AS1, ZNF341 (L740P +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2216427	NM_001282933.2(ZNF341):c.2107C>T (p.Arg703Cys)	ZNF341, ZNF341-AS1 (R613C +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2194428	NM_001282933.2(ZNF341):c.2000C>T (p.Pro667Leu)	ZNF341, ZNF341-AS1 (P577L +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2190089	NM_001282933.2(ZNF341):c.2149G>A (p.Ala717Thr)	ZNF341-AS1, ZNF341 (A627T +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2182815	NM_001282933.2(ZNF341):c.1968G>A (p.Thr656=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2180683	NM_001282933.2(ZNF341):c.2433G>A (p.Ala811=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2161342	NM_001282933.2(ZNF341):c.2069A>G (p.Lys690Arg)	ZNF341-AS1, ZNF341 (K600R +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2160306	NM_001282933.2(ZNF341):c.2237C>A (p.Pro746His)	ZNF341, ZNF341-AS1 (P746H +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 2152329	NM_001282933.2(ZNF341):c.1967C>T (p.Thr656Met)	ZNF341, ZNF341-AS1 (T566M +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2149698	NM_001282933.2(ZNF341):c.2261G>A (p.Arg754His)	ZNF341, ZNF341-AS1 (R664H +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2125299	NM_001282933.2(ZNF341):c.2007G>A (p.Lys669=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2111044	NM_001282933.2(ZNF341):c.1965-15G>T	ZNF341, ZNF341-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2109712	NM_001282933.2(ZNF341):c.1921_1922del (p.Met641fs)	ZNF341, ZNF341-AS1 (M634fs +2 more)	Deletion (frameshift variant +1 more)	not provided	GPathogenic
Select item 2103961	NM_001282933.2(ZNF341):c.1857G>A (p.Glu619=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2096425	NM_001282933.2(ZNF341):c.2543T>C (p.Val848Ala)	ZNF341, ZNF341-AS1 (V841A +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2092185	NM_001282933.2(ZNF341):c.1916G>A (p.Arg639Lys)	ZNF341, ZNF341-AS1 (R549K +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2090453	NM_001282933.2(ZNF341):c.2391G>C (p.Pro797=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2090261	NM_001282933.2(ZNF341):c.1943A>G (p.Lys648Arg)	ZNF341, ZNF341-AS1 (K648R +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2089077	NM_001282933.2(ZNF341):c.1988A>G (p.Glu663Gly)	ZNF341, ZNF341-AS1 (E656G +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2076569	NM_001282933.2(ZNF341):c.1890G>T (p.Ala630=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2076237	NM_001282933.2(ZNF341):c.2424G>T (p.Ala808=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2074205	NM_001282933.2(ZNF341):c.2395G>A (p.Ala799Thr)	ZNF341, ZNF341-AS1 (A709T +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2071777	NM_001282933.2(ZNF341):c.1965-7G>A	ZNF341, ZNF341-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2050661	NM_001282933.2(ZNF341):c.2533G>A (p.Ala845Thr)	ZNF341, ZNF341-AS1 (A838T +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2049839	NM_001282933.2(ZNF341):c.2035+15G>C	ZNF341, ZNF341-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2012590	NM_001282933.2(ZNF341):c.1963T>C (p.Ser655Pro)	ZNF341, ZNF341-AS1 (S648P +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2005806	NM_001282933.2(ZNF341):c.2007G>C (p.Lys669Asn)	ZNF341, ZNF341-AS1 (K579N +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1996738	NM_001282933.2(ZNF341):c.2452C>G (p.Pro818Ala)	ZNF341, ZNF341-AS1 (P728A +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1994470	NM_001282933.2(ZNF341):c.2475C>T (p.Gly825=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1989003	NM_001282933.2(ZNF341):c.2097C>T (p.Ala699=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1984733	NM_001282933.2(ZNF341):c.2112C>T (p.Ala704=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1974116	NM_001282933.2(ZNF341):c.2296C>T (p.Pro766Ser)	ZNF341, ZNF341-AS1 (P759S +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1959509	NM_001282933.2(ZNF341):c.2157C>T (p.Gly719=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1958673	NM_001282933.2(ZNF341):c.2360C>G (p.Ala787Gly)	ZNF341, ZNF341-AS1 (A780G +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1955154	NM_001282933.2(ZNF341):c.1964C>T (p.Ser655Leu)	ZNF341-AS1, ZNF341 (S565L +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1951681	NM_001282933.2(ZNF341):c.2432C>A (p.Ala811Glu)	ZNF341, ZNF341-AS1 (A721E +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1951522	NM_001282933.2(ZNF341):c.1979G>A (p.Cys660Tyr)	ZNF341, ZNF341-AS1 (C570Y +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1949775	NM_001282933.2(ZNF341):c.2555C>T (p.Ala852Val)	ZNF341, ZNF341-AS1 (A852V +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1946673	NM_001282933.2(ZNF341):c.2089C>T (p.His697Tyr)	ZNF341, ZNF341-AS1 (H697Y +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1935820	NM_001282933.2(ZNF341):c.2055C>T (p.Cys685=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1934556	NM_001282933.2(ZNF341):c.2036-13C>T	ZNF341, ZNF341-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1928648	NM_001282933.2(ZNF341):c.2421T>G (p.Gly807=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1925799	NM_001282933.2(ZNF341):c.2479A>G (p.Asn827Asp)	ZNF341, ZNF341-AS1 (N737D +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1910334	NM_001282933.2(ZNF341):c.2529G>T (p.Met843Ile)	ZNF341, ZNF341-AS1 (M836I +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1909980	NM_001282933.2(ZNF341):c.2233C>T (p.Arg745Trp)	ZNF341, ZNF341-AS1 (R655W +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1907521	NM_001282933.2(ZNF341):c.2275G>C (p.Gly759Arg)	ZNF341, ZNF341-AS1 (G759R +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1907037	NM_001282933.2(ZNF341):c.2167C>T (p.His723Tyr)	ZNF341, ZNF341-AS1 (H716Y +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 1903311	NM_001282933.2(ZNF341):c.2165G>T (p.Arg722Leu)	ZNF341, ZNF341-AS1 (R715L +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1897019	NM_001282933.2(ZNF341):c.2559C>T (p.Ser853=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1672434	NM_001282933.2(ZNF341):c.2391G>A (p.Pro797=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1661808	NM_001282933.2(ZNF341):c.1860G>A (p.Lys620=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1656076	NM_001282933.2(ZNF341):c.2454T>C (p.Pro818=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1649563	NM_001282933.2(ZNF341):c.2542G>A (p.Val848Ile)	ZNF341, ZNF341-AS1 (V758I +2 more)	Single nucleotide variant (missense variant +1 more)	Hyper-IgE recurrent infection syndrome 3, autosomal recessive +1 more	GConflicting classifications of pathogenicity
Select item 1621468	NM_001282933.2(ZNF341):c.2082C>T (p.Arg694=)	ZNF341-AS1, ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1616372	NM_001282933.2(ZNF341):c.1938C>T (p.Pro646=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1611285	NM_001282933.2(ZNF341):c.2259C>T (p.Pro753=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 1608480	NM_001282933.2(ZNF341):c.2376G>A (p.Pro792=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1607307	NM_001282933.2(ZNF341):c.2328G>A (p.Leu776=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1600415	NM_001282933.2(ZNF341):c.2423C>T (p.Ala808Val)	ZNF341, ZNF341-AS1 (A718V +2 more)	Single nucleotide variant (missense variant +1 more)	ZNF341-related condition +1 more	GBenign
Select item 1599824	NM_001282933.2(ZNF341):c.2166C>T (p.Arg722=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1592020	NM_001282933.2(ZNF341):c.1962C>T (p.Phe654=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1589706	NM_001282933.2(ZNF341):c.2532C>T (p.Leu844=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	ZNF341-related condition +1 more	GLikely benign

<< First< Prev

Page of 2