List of variants in gene ZNF335 reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 39

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HGVS	dbSNP	gnomAD frequency
NM_022095.4(ZNF335):c.3187C>A (p.Arg1063=)	rs11905235	0.02316
NM_022095.4(ZNF335):c.2167T>G (p.Phe723Val)	rs41305805	0.01608
NM_022095.4(ZNF335):c.442+67T>C	rs115355976	0.01259
NM_022095.4(ZNF335):c.1102+9T>C	rs112458662	0.00945
NM_022095.4(ZNF335):c.3800C>A (p.Pro1267Gln)	rs113958814	0.00829
NM_022095.4(ZNF335):c.1963C>T (p.Pro655Ser)	rs117132825	0.00766
NM_022095.4(ZNF335):c.201+296A>G	rs145802687	0.00716
NM_022095.4(ZNF335):c.3180C>T (p.Pro1060=)	rs61729182	0.00669
NM_022095.4(ZNF335):c.1356-32C>T	rs142226722	0.00648
NM_022095.4(ZNF335):c.3489T>C (p.Thr1163=)	rs116077790	0.00620
NM_022095.4(ZNF335):c.2254-214C>A	rs139689930	0.00561
NM_022095.4(ZNF335):c.2821G>A (p.Ala941Thr)	rs116247914	0.00511
NM_022095.4(ZNF335):c.2702+54C>T	rs141323614	0.00459
NM_022095.4(ZNF335):c.3507C>T (p.His1169=)	rs141812371	0.00420
NM_022095.4(ZNF335):c.1647-159G>A	rs138395446	0.00416
NM_022095.4(ZNF335):c.3487+46G>C	rs115628563	0.00403
NM_022095.4(ZNF335):c.2253+255G>A	rs116243696	0.00402
NM_022095.4(ZNF335):c.-50-17G>A	rs181753695	0.00401
NM_022095.4(ZNF335):c.956-246C>T	rs77340136	0.00401
NM_022095.4(ZNF335):c.2020+166A>T	rs116326494	0.00397
NM_022095.4(ZNF335):c.955+133G>A	rs114670028	0.00394
NM_022095.4(ZNF335):c.2021-31G>C	rs116816891	0.00382
NM_022095.4(ZNF335):c.2986A>G (p.Thr996Ala)	rs146217460	0.00316
NM_022095.4(ZNF335):c.103G>T (p.Val35Leu)	rs114356103	0.00300
NM_022095.4(ZNF335):c.3592-33G>C	rs201495017	0.00265
NM_022095.4(ZNF335):c.-50-45G>T	rs527700402	0.00198
NM_022095.4(ZNF335):c.3820-11C>T	rs191147826	0.00194
NM_022095.4(ZNF335):c.-50-50G>A	rs552261090	0.00187
NM_022095.4(ZNF335):c.3392G>A (p.Arg1131Lys)	rs114864530	0.00119
NM_022095.4(ZNF335):c.2185A>T (p.Ile729Phe)	rs190178539	0.00039
NM_022095.4(ZNF335):c.3843A>G (p.Pro1281=)	rs35291173	0.00016
NM_022095.4(ZNF335):c.2414A>G (p.Gln805Arg)	rs199704102	0.00010
NM_022095.4(ZNF335):c.1930G>A (p.Val644Ile)	rs140668957	0.00008
NM_022095.4(ZNF335):c.2500C>T (p.Pro834Ser)	rs549937846	0.00008
NM_022095.4(ZNF335):c.857G>A (p.Arg286Gln)	rs559354455	0.00007
NM_022095.4(ZNF335):c.1552G>A (p.Val518Met)	rs768453184	0.00002
NM_022095.4(ZNF335):c.1665G>A (p.Pro555=)	rs1201395437	0.00001
NM_022095.4(ZNF335):c.*278G>C	rs3363
NM_022095.4(ZNF335):c.3670-16dup	rs201440041

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