"GeneDx"[submitter] AND "ZNF335"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1231704	NM_022095.4(ZNF335):c.*278G>A	ZNF335	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1197755	NM_022095.4(ZNF335):c.*278G>C	ZNF335	Single nucleotide variant (3 prime UTR variant)	not provided	GLikely benign
Select item 453188	NM_022095.4(ZNF335):c.3998A>G (p.Glu1333Gly)	ZNF335 (E1333G)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2580439	NM_022095.4(ZNF335):c.3984G>C (p.Gln1328His)	ZNF335 (Q1328H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 212652	NM_022095.4(ZNF335):c.3843A>G (p.Pro1281=)	ZNF335	Single nucleotide variant (synonymous variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1208693	NM_022095.4(ZNF335):c.3820-11C>T	ZNF335	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 791209	NM_022095.4(ZNF335):c.3800C>A (p.Pro1267Gln)	ZNF335 (P1267Q)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1309123	NM_022095.4(ZNF335):c.3757C>G (p.Gln1253Glu)	ZNF335 (Q1253E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 787492	NM_022095.4(ZNF335):c.3670-16dup	ZNF335	Duplication (intron variant)	Microcephalic primordial dwarfism due to ZNF335 deficiency +1 more	GBenign/Likely benign
Select item 1196229	NM_022095.4(ZNF335):c.3592-33G>C	ZNF335	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 130806	NM_022095.4(ZNF335):c.3522A>T (p.Pro1174=)	ZNF335	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 130805	NM_022095.4(ZNF335):c.3507C>T (p.His1169=)	ZNF335	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 716509	NM_022095.4(ZNF335):c.3489T>C (p.Thr1163=)	ZNF335	Single nucleotide variant (synonymous variant)	Microcephalic primordial dwarfism due to ZNF335 deficiency +1 more	GBenign/Likely benign
Select item 1261468	NM_022095.4(ZNF335):c.3488-68T>C	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1216206	NM_022095.4(ZNF335):c.3487+46G>C	ZNF335	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1170657	NM_022095.4(ZNF335):c.3487+14G>C	ZNF335	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 130804	NM_022095.4(ZNF335):c.3392G>A (p.Arg1131Lys)	ZNF335 (R1131K)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 130803	NM_022095.4(ZNF335):c.3384T>C (p.Pro1128=)	ZNF335	Single nucleotide variant (synonymous variant)	Microcephalic primordial dwarfism due to ZNF335 deficiency +1 more	GBenign
Select item 779473	NM_022095.4(ZNF335):c.3354C>T (p.Leu1118=)	ZNF335	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1303440	NM_022095.4(ZNF335):c.3351C>A (p.His1117Gln)	ZNF335 (H1117Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 130802	NM_022095.4(ZNF335):c.3187C>A (p.Arg1063=)	ZNF335	Single nucleotide variant (synonymous variant)	Microcephalic primordial dwarfism due to ZNF335 deficiency +2 more	GBenign/Likely benign
Select item 130801	NM_022095.4(ZNF335):c.3180C>T (p.Pro1060=)	ZNF335	Single nucleotide variant (synonymous variant)	Microcephalic primordial dwarfism due to ZNF335 deficiency +1 more	GBenign/Likely benign
Select item 2977763	NM_022095.4(ZNF335):c.3023C>T (p.Pro1008Leu)	ZNF335 (P1008L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 712868	NM_022095.4(ZNF335):c.2986A>G (p.Thr996Ala)	ZNF335 (T996A)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 130800	NM_022095.4(ZNF335):c.2821G>A (p.Ala941Thr)	ZNF335 (A941T)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 1307280	NM_022095.4(ZNF335):c.2814G>A (p.Glu938=)	ZNF335	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 375393	NM_022095.4(ZNF335):c.2744_2747del (p.Ser915fs)	ZNF335 (S915fs)	Microsatellite (frameshift variant)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 130799	NM_022095.4(ZNF335):c.2703C>T (p.Ser901=)	ZNF335	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1230316	NM_022095.4(ZNF335):c.2703-105G>C	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264193	NM_022095.4(ZNF335):c.2702+324C>G	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1252469	NM_022095.4(ZNF335):c.2702+141T>A	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1301160	NM_022095.4(ZNF335):c.2702+54C>T	ZNF335	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 130798	NM_022095.4(ZNF335):c.2595C>A (p.Asp865Glu)	ZNF335 (D865E)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1165196	NM_022095.4(ZNF335):c.2500C>T (p.Pro834Ser)	ZNF335 (P834S)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1183331	NM_022095.4(ZNF335):c.2443-249G>A	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242138	NM_022095.4(ZNF335):c.2442+202G>A	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242335	NM_022095.4(ZNF335):c.2442+189C>T	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2430767	NM_022095.4(ZNF335):c.2429G>A (p.Gly810Asp)	ZNF335 (G810D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 719053	NM_022095.4(ZNF335):c.2414A>G (p.Gln805Arg)	ZNF335 (Q805R)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2580040	NM_022095.4(ZNF335):c.2359T>A (p.Ser787Thr)	ZNF335 (S787T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1261214	NM_022095.4(ZNF335):c.2254-140dup	ZNF335	Duplication (intron variant)	not provided	GBenign
Select item 1206886	NM_022095.4(ZNF335):c.2254-214C>A	ZNF335	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1202863	NM_022095.4(ZNF335):c.2253+255G>A	ZNF335	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1222982	NM_022095.4(ZNF335):c.2253+39C>T	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 130797	NM_022095.4(ZNF335):c.2253+10G>T	ZNF335	Single nucleotide variant (intron variant)	Microcephalic primordial dwarfism due to ZNF335 deficiency +1 more	GBenign
Select item 624195	NM_022095.4(ZNF335):c.2185A>T (p.Ile729Phe)	ZNF335 (I729F)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 212644	NM_022095.4(ZNF335):c.2168TCT[1] (p.Phe724del)	ZNF335 (F724del)	Microsatellite (inframe_deletion)	not provided +1 more	GUncertain significance
Select item 130796	NM_022095.4(ZNF335):c.2167T>G (p.Phe723Val)	ZNF335 (F723V)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1220270	NM_022095.4(ZNF335):c.2021-31G>C	ZNF335	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1287055	NM_022095.4(ZNF335):c.2021-37C>T	ZNF335	Single nucleotide variant (intron variant)	Microcephalic primordial dwarfism due to ZNF335 deficiency +1 more	GBenign
Select item 1290424	NM_022095.4(ZNF335):c.2021-74G>C	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249226	NM_022095.4(ZNF335):c.2021-107C>T	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229203	NM_022095.4(ZNF335):c.2021-169A>G	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229504	NM_022095.4(ZNF335):c.2021-210G>C	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1259534	NM_022095.4(ZNF335):c.2021-333T>C	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1203182	NM_022095.4(ZNF335):c.2020+166A>T	ZNF335	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1259622	NM_022095.4(ZNF335):c.2020+80del	ZNF335	Deletion (intron variant)	not provided	GBenign
Select item 1290629	NM_022095.4(ZNF335):c.2020+31C>G	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 212643	NM_022095.4(ZNF335):c.1963C>T (p.Pro655Ser)	ZNF335 (P655S)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1190756	NM_022095.4(ZNF335):c.1930G>A (p.Val644Ile)	ZNF335 (V644I)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 817743	NM_022095.4(ZNF335):c.1887_1890del (p.Cys630fs)	ZNF335 (C630fs)	Microsatellite (frameshift variant)	not provided	GLikely pathogenic
Select item 1304739	NM_022095.4(ZNF335):c.1736A>G (p.Gln579Arg)	ZNF335 (Q579R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1706296	NM_022095.4(ZNF335):c.1678A>T (p.Ser560Cys)	ZNF335 (S560C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1309032	NM_022095.4(ZNF335):c.1665G>A (p.Pro555=)	ZNF335	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1300300	NM_022095.4(ZNF335):c.1647-159G>A	ZNF335	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1289421	NM_022095.4(ZNF335):c.1647-321G>T	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 437349	NM_022095.4(ZNF335):c.1646+5G>T	ZNF335	Single nucleotide variant (intron variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 130794	NM_022095.4(ZNF335):c.1623C>T (p.His541=)	ZNF335	Single nucleotide variant (synonymous variant)	Microcephalic primordial dwarfism due to ZNF335 deficiency +1 more	GBenign
Select item 1203489	NM_022095.4(ZNF335):c.1552G>A (p.Val518Met)	ZNF335 (V518M)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 1289025	NM_022095.4(ZNF335):c.1534-268C>G	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1214548	NM_022095.4(ZNF335):c.1516C>T (p.Arg506Cys)	ZNF335 (R506C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1327401	NM_022095.4(ZNF335):c.1447C>T (p.His483Tyr)	ZNF335 (H483Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1186803	NM_022095.4(ZNF335):c.1418G>A (p.Arg473His)	ZNF335 (R473H)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 1217663	NM_022095.4(ZNF335):c.1356-32C>T	ZNF335	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1170104	NM_022095.4(ZNF335):c.1355+13G>A	ZNF335	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 130791	NM_022095.4(ZNF335):c.1103-7G>A	ZNF335	Single nucleotide variant (intron variant)	Microcephalic primordial dwarfism due to ZNF335 deficiency +1 more	GBenign
Select item 1276672	NM_022095.4(ZNF335):c.1103-327G>A	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1224935	NM_022095.4(ZNF335):c.1102+39C>T	ZNF335	Single nucleotide variant (intron variant)	Microcephalic primordial dwarfism due to ZNF335 deficiency +1 more	GBenign
Select item 446071	NM_022095.4(ZNF335):c.1102+9T>C	ZNF335	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 1182671	NM_022095.4(ZNF335):c.956-162G>A	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1224937	NM_022095.4(ZNF335):c.956-182C>T	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1217881	NM_022095.4(ZNF335):c.956-246C>T	ZNF335	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1281642	NM_022095.4(ZNF335):c.956-313A>G	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1199005	NM_022095.4(ZNF335):c.955+133G>A	ZNF335	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 130810	NM_022095.4(ZNF335):c.881G>C (p.Ser294Thr)	ZNF335 (S294T)	Single nucleotide variant (missense variant)	Microcephalic primordial dwarfism due to ZNF335 deficiency +1 more	GBenign
Select item 1678808	NM_022095.4(ZNF335):c.857G>A (p.Arg286Gln)	ZNF335 (R286Q)	Single nucleotide variant (missense variant)	Microcephalic primordial dwarfism due to ZNF335 deficiency +1 more	GConflicting classifications of pathogenicity
Select item 130809	NM_022095.4(ZNF335):c.826G>A (p.Ala276Thr)	ZNF335 (A276T)	Single nucleotide variant (missense variant)	Microcephalic primordial dwarfism due to ZNF335 deficiency +2 more	GBenign/Likely benign
Select item 130808	NM_022095.4(ZNF335):c.815-3del	ZNF335	Deletion (intron variant)	Microcephalic primordial dwarfism due to ZNF335 deficiency +2 more	GBenign
Select item 1235889	NM_022095.4(ZNF335):c.814+46G>A	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 130807	NM_022095.4(ZNF335):c.642C>T (p.Ser214=)	ZNF335	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 1247136	NM_022095.4(ZNF335):c.442+131del	ZNF335	Deletion (intron variant)	not provided	GBenign
Select item 1185945	NM_022095.4(ZNF335):c.442+67T>C	ZNF335	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1327335	NM_022095.4(ZNF335):c.304G>A (p.Gly102Ser)	ZNF335 (G102S)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1183677	NM_022095.4(ZNF335):c.202-340A>G	ZNF335	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1189434	NM_022095.4(ZNF335):c.201+296A>G	ZNF335	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2430843	NM_022095.4(ZNF335):c.185G>A (p.Arg62His)	ZNF335 (R62H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 437356	NM_022095.4(ZNF335):c.147_152dup (p.Glu50_Ala51dup)	ZNF335	Duplication (inframe_insertion)	not provided +1 more	GUncertain significance
Select item 2056625	NM_022095.4(ZNF335):c.131C>G (p.Ala44Gly)	ZNF335 (A44G)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 709516	NM_022095.4(ZNF335):c.103G>T (p.Val35Leu)	ZNF335 (V35L)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 2219696	NM_022095.4(ZNF335):c.91A>C (p.Thr31Pro)	ZNF335 (T31P)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance

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