ClinVar for Gene (Select 84905) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3335548	NM_001282933.2(ZNF341):c.2150C>T (p.Ala717Val)	ZNF341, ZNF341-AS1 (A710V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335547	NM_001282933.2(ZNF341):c.307G>A (p.Val103Ile)	ZNF341 (V103I)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3335546	NM_001282933.2(ZNF341):c.2356G>A (p.Glu786Lys)	ZNF341, ZNF341-AS1 (E696K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3248359	NC_000020.10:g.(?_32349648)_(32349881_?)dup	ZNF341	Duplication	not provided	GLikely pathogenic
Select item 3248358	NC_000020.10:g.(?_32354637)_(32354867_?)del	ZNF341	Deletion	not provided	GPathogenic
Select item 3248357	NC_000020.10:g.(?_32369077)_(32369213_?)del	ZNF341	Deletion	not provided	GPathogenic
Select item 3248356	NC_000020.10:g.(?_32319828)_(32379323_?)del	ZNF341	Deletion	not provided	GPathogenic
Select item 3248297	NC_000020.10:g.(?_31571600)_(33001705_?)del	ACTL10, AHCY +22 more	Deletion	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase	GPathogenic
Select item 3248260	NC_000020.10:g.(?_31368130)_(34287210_?)del	ACSS2, ACTL10 +51 more	Deletion	Glutathione synthetase deficiency with 5-oxoprolinuria	GPathogenic
Select item 3195292	NM_001282933.2(ZNF341):c.995C>T (p.Thr332Ile)	ZNF341 (T242I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195291	NM_001282933.2(ZNF341):c.977A>G (p.Tyr326Cys)	ZNF341 (Y319C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195289	NM_001282933.2(ZNF341):c.535C>T (p.Pro179Ser)	ZNF341 (P179S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195288	NM_001282933.2(ZNF341):c.28G>C (p.Glu10Gln)	LOC130065694, ZNF341 (E10Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3195287	NM_001282933.2(ZNF341):c.2506G>A (p.Gly836Arg)	ZNF341, ZNF341-AS1 (G829R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195286	NM_001282933.2(ZNF341):c.2014G>A (p.Ala672Thr)	ZNF341, ZNF341-AS1 (A582T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195285	NM_001282933.2(ZNF341):c.111T>A (p.Ser37Arg)	ZNF341 (V13E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3042456	NM_001282933.2(ZNF341):c.-7C>T	LOC130065694, ZNF341	Single nucleotide variant (5 prime UTR variant +1 more)	ZNF341-related disorder	GBenign
Select item 3021163	NM_001282933.2(ZNF341):c.1414G>A (p.Val472Met)	ZNF341 (V465M +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3020745	NM_001282933.2(ZNF341):c.72G>A (p.Leu24=)	ZNF341	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 3017809	NM_001282933.2(ZNF341):c.1761C>T (p.Thr587=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3016212	NM_001282933.2(ZNF341):c.489+9G>A	ZNF341	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3011938	NM_001282933.2(ZNF341):c.1881C>T (p.Cys627=)	ZNF341, ZNF341-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3011385	NM_001282933.2(ZNF341):c.941C>A (p.Ala314Glu)	ZNF341 (A307E +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3010923	NM_001282933.2(ZNF341):c.741+13G>A	ZNF341	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3007227	NM_001282933.2(ZNF341):c.741+15C>A	ZNF341	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3005668	NM_001282933.2(ZNF341):c.1199G>A (p.Arg400Lys)	ZNF341 (R310K +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
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 3003693	NM_001282933.2(ZNF341):c.1629C>T (p.Val543=)	ZNF341	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3002937	NM_001282933.2(ZNF341):c.1092T>C (p.Asn364=)	ZNF341	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 3000089	NM_001282933.2(ZNF341):c.996C>T (p.Thr332=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	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-AS1, ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2997924	NM_001282933.2(ZNF341):c.48C>T (p.Thr16=)	ZNF341	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2997233	NM_001282933.2(ZNF341):c.241C>G (p.Pro81Ala)	ZNF341 (P81A)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
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 2991599	NM_001282933.2(ZNF341):c.1536C>A (p.Phe512Leu)	ZNF341 (F505L +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2990732	NM_001282933.2(ZNF341):c.1509C>T (p.Tyr503=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2989599	NM_001282933.2(ZNF341):c.894G>T (p.Thr298=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2980711	NM_001282933.2(ZNF341):c.1581C>G (p.Leu527=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
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 2979778	NM_001282933.2(ZNF341):c.1413+7G>A	ZNF341	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2979083	NM_001282933.2(ZNF341):c.1643A>G (p.Lys548Arg)	ZNF341 (K541R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2976032	NM_001282933.2(ZNF341):c.192G>A (p.Ser64=)	ZNF341	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2975919	NM_001282933.2(ZNF341):c.1222+19C>T	ZNF341	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2974862	NM_001282933.2(ZNF341):c.894G>A (p.Thr298=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
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 (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2965989	NM_001282933.2(ZNF341):c.143-18C>A	ZNF341	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2965828	NM_001282933.2(ZNF341):c.31+12_31+23dup	LOC130065694, ZNF341	Duplication (intron variant)	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 2964964	NM_001282933.2(ZNF341):c.801C>A (p.Gly267=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2962005	NM_001282933.2(ZNF341):c.1028+11G>A	ZNF341	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2959077	NM_001282933.2(ZNF341):c.31+24_31+29dup	LOC130065694, ZNF341	Duplication (intron variant)	not provided	GLikely benign
Select item 2957891	NM_001282933.2(ZNF341):c.1110G>A (p.Gln370=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2956582	NM_001282933.2(ZNF341):c.340-8C>A	ZNF341	Single nucleotide variant (intron variant)	not provided	GLikely benign
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 2916171	NM_001282933.2(ZNF341):c.925G>A (p.Gly309Arg)	ZNF341 (G309R +1 more)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 2909477	NM_001282933.2(ZNF341):c.1811G>A (p.Arg604Gln)	ZNF341 (R514Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
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 2905365	NM_001282933.2(ZNF341):c.1209C>T (p.Asp403=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2904955	NM_001282933.2(ZNF341):c.1539C>T (p.Pro513=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2904067	NM_001282933.2(ZNF341):c.1530G>A (p.Lys510=)	ZNF341	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 2888003	NM_001282933.2(ZNF341):c.783C>A (p.Pro261=)	ZNF341	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 2876345	NM_001282933.2(ZNF341):c.1062A>G (p.Ala354=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2875101	NM_001282933.2(ZNF341):c.825A>G (p.Gly275=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
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 2842725	NM_001282933.2(ZNF341):c.938-7C>A	ZNF341	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2833008	NM_001282933.2(ZNF341):c.659T>C (p.Val220Ala)	ZNF341 (V130A +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2828923	NM_001282933.2(ZNF341):c.1428G>A (p.Val476=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2817047	NM_001282933.2(ZNF341):c.1852+15C>G	ZNF341	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2816513	NM_001282933.2(ZNF341):c.31+15_31+26dup	LOC130065694, ZNF341	Duplication (intron variant)	not provided	GLikely benign
Select item 2810620	NM_001282933.2(ZNF341):c.1365C>T (p.Ser455=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2804550	NM_001282933.2(ZNF341):c.1653C>T (p.Thr551=)	ZNF341	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2796548	NM_001282933.2(ZNF341):c.98C>T (p.Pro33Leu)	ZNF341 (R9* +1 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GConflicting classifications of pathogenicity
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 2792431	NM_001282933.2(ZNF341):c.1206G>A (p.Glu402=)	ZNF341	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 2784482	NM_001282933.2(ZNF341):c.284C>T (p.Pro95Leu)	ZNF341 (P95L)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2778284	NM_001282933.2(ZNF341):c.240C>T (p.Ala80=)	ZNF341	Single nucleotide variant (synonymous variant +2 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 2771573	NM_001282933.2(ZNF341):c.1852+1G>A	ZNF341	Single nucleotide variant (splice donor variant)	not provided	GLikely pathogenic
Select item 2763709	NM_001282933.2(ZNF341):c.627T>C (p.Arg209=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2759918	NM_001282933.2(ZNF341):c.567C>T (p.Pro189=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2752004	NM_001282933.2(ZNF341):c.90C>A (p.Val30=)	ZNF341 (S6Y)	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2750284	NM_001282933.2(ZNF341):c.951A>G (p.Pro317=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2732393	NM_001282933.2(ZNF341):c.92del (p.Pro31fs)	ZNF341 (P31fs)	Deletion (frameshift variant +2 more)	not provided	GPathogenic
Select item 2729072	NM_001282933.2(ZNF341):c.31+17C>T	LOC130065694, ZNF341	Single nucleotide variant (intron variant)	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 2722790	NM_001282933.2(ZNF341):c.618C>T (p.Pro206=)	ZNF341	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2720009	NM_001282933.2(ZNF341):c.1637T>C (p.Val546Ala)	ZNF341 (V539A +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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