ClinVar Miner

List of variants in gene ZNF462 reported as uncertain significance for Weiss-Kruszka syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 35
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_021224.6(ZNF462):c.4261G>A (p.Glu1421Lys) rs146639350 0.00013
NM_021224.6(ZNF462):c.4087C>T (p.Pro1363Ser) rs374016854 0.00004
NM_021224.6(ZNF462):c.6601G>A (p.Gly2201Ser) rs1240557088 0.00002
NM_021224.6(ZNF462):c.4241A>T (p.Glu1414Val) rs779040674 0.00001
NM_021224.6(ZNF462):c.-31+644G>C
NM_021224.6(ZNF462):c.1173G>C (p.Glu391Asp) rs1830136626
NM_021224.6(ZNF462):c.1298G>C (p.Arg433Thr)
NM_021224.6(ZNF462):c.2339A>G (p.Asp780Gly) rs1830188459
NM_021224.6(ZNF462):c.2402A>G (p.Tyr801Cys)
NM_021224.6(ZNF462):c.2760C>G (p.His920Gln)
NM_021224.6(ZNF462):c.2926A>G (p.Thr976Ala)
NM_021224.6(ZNF462):c.2966C>T (p.Ala989Val)
NM_021224.6(ZNF462):c.3047G>A (p.Cys1016Tyr) rs1422121486
NM_021224.6(ZNF462):c.3060G>C (p.Lys1020Asn) rs2131477184
NM_021224.6(ZNF462):c.3160C>G (p.Pro1054Ala)
NM_021224.6(ZNF462):c.3220A>G (p.Arg1074Gly)
NM_021224.6(ZNF462):c.3292_3293insGGCCCCCCCCCCCCCCCCC (p.Ser1098fs)
NM_021224.6(ZNF462):c.3478G>A (p.Val1160Ile)
NM_021224.6(ZNF462):c.3601G>A (p.Gly1201Arg) rs1330178325
NM_021224.6(ZNF462):c.3880A>G (p.Thr1294Ala)
NM_021224.6(ZNF462):c.3965C>T (p.Thr1322Met)
NM_021224.6(ZNF462):c.4147G>C (p.Asp1383His)
NM_021224.6(ZNF462):c.4252C>G (p.Leu1418Val) rs758226459
NM_021224.6(ZNF462):c.4390G>A (p.Ala1464Thr)
NM_021224.6(ZNF462):c.4588G>T (p.Val1530Leu) rs762506887
NM_021224.6(ZNF462):c.4733G>A (p.Arg1578Gln)
NM_021224.6(ZNF462):c.4759G>T (p.Gly1587Cys)
NM_021224.6(ZNF462):c.4885C>T (p.Pro1629Ser) rs2131506841
NM_021224.6(ZNF462):c.5284C>G (p.Arg1762Gly)
NM_021224.6(ZNF462):c.5771G>A (p.Arg1924His)
NM_021224.6(ZNF462):c.5797A>T (p.Ser1933Cys)
NM_021224.6(ZNF462):c.6013-11T>A
NM_021224.6(ZNF462):c.6227C>T (p.Ala2076Val)
NM_021224.6(ZNF462):c.6303C>G (p.His2101Gln)
NM_021224.6(ZNF462):c.6571C>T (p.Leu2191Phe)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.