ClinVar Miner

List of variants in gene ZNF676 reported as uncertain significance

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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_001001411.3(ZNF676):c.1124G>A (p.Ser375Asn) rs200273136 0.00106
NM_001001411.3(ZNF676):c.172G>A (p.Gly58Ser) rs189442130 0.00046
NM_001001411.3(ZNF676):c.560A>G (p.Tyr187Cys) rs371456888 0.00046
NM_001001411.3(ZNF676):c.1405A>G (p.Arg469Gly) rs200365534 0.00036
NM_001001411.3(ZNF676):c.164C>T (p.Pro55Leu) rs199670498 0.00026
NM_001001411.3(ZNF676):c.430A>G (p.Lys144Glu) rs192725054 0.00014
NM_001001411.3(ZNF676):c.1463C>T (p.Thr488Met) rs372702194 0.00013
NM_001001411.3(ZNF676):c.788G>C (p.Ser263Thr) rs1291774986 0.00012
NM_001001411.3(ZNF676):c.1702A>G (p.Lys568Glu) rs774878650 0.00011
NM_001001411.3(ZNF676):c.183T>G (p.Asp61Glu) rs549335423 0.00011
NM_001001411.3(ZNF676):c.229G>C (p.Glu77Gln) rs756136777 0.00011
NM_001001411.3(ZNF676):c.1175C>T (p.Pro392Leu) rs199601535 0.00008
NM_001001411.3(ZNF676):c.361G>A (p.Val121Ile) rs376158454 0.00008
NM_001001411.3(ZNF676):c.277G>A (p.Val93Met) rs184119584 0.00006
NM_001001411.3(ZNF676):c.1153G>A (p.Ala385Thr) rs746950296 0.00005
NM_001001411.3(ZNF676):c.1471A>G (p.Ile491Val) rs200330533 0.00004
NM_001001411.3(ZNF676):c.1445G>A (p.Cys482Tyr) rs763929340 0.00003
NM_001001411.3(ZNF676):c.343T>C (p.Cys115Arg) rs938116360 0.00003
NM_001001411.3(ZNF676):c.390A>T (p.Arg130Ser) rs772808312 0.00003
NM_001001411.3(ZNF676):c.770A>G (p.Glu257Gly) rs200737633 0.00003
NM_001001411.3(ZNF676):c.1115A>G (p.Lys372Arg) rs761280683 0.00002
NM_001001411.3(ZNF676):c.1320G>C (p.Lys440Asn) rs752044501 0.00002
NM_001001411.3(ZNF676):c.176T>C (p.Ile59Thr) rs367723653 0.00002
NM_001001411.3(ZNF676):c.1196G>A (p.Gly399Asp) rs369300351 0.00001
NM_001001411.3(ZNF676):c.1285G>T (p.Ala429Ser) rs201835667 0.00001
NM_001001411.3(ZNF676):c.1660A>T (p.Ile554Phe) rs2023708668 0.00001
NM_001001411.3(ZNF676):c.211T>C (p.Tyr71His) rs2023751571 0.00001
NM_001001411.3(ZNF676):c.582G>C (p.Glu194Asp) rs765582913 0.00001
NM_001001411.3(ZNF676):c.662G>T (p.Gly221Val) rs1156963536 0.00001
NM_001001411.3(ZNF676):c.982A>G (p.Lys328Glu) rs369672319 0.00001
NM_001001411.3(ZNF676):c.1094A>G (p.Tyr365Cys)
NM_001001411.3(ZNF676):c.1112G>A (p.Gly371Asp)
NM_001001411.3(ZNF676):c.1156A>G (p.Ile386Val)
NM_001001411.3(ZNF676):c.1184G>C (p.Cys395Ser)
NM_001001411.3(ZNF676):c.1274A>T (p.Glu425Val)
NM_001001411.3(ZNF676):c.1380G>T (p.Trp460Cys)
NM_001001411.3(ZNF676):c.1411C>A (p.His471Asn)
NM_001001411.3(ZNF676):c.1495C>G (p.His499Asp)
NM_001001411.3(ZNF676):c.1496A>G (p.His499Arg) rs1372993570
NM_001001411.3(ZNF676):c.1562C>A (p.Thr521Asn)
NM_001001411.3(ZNF676):c.1582A>G (p.Thr528Ala)
NM_001001411.3(ZNF676):c.1627A>C (p.Ser543Arg) rs956826116
NM_001001411.3(ZNF676):c.1741A>G (p.Lys581Glu) rs1301937233
NM_001001411.3(ZNF676):c.226C>T (p.His76Tyr) rs2023751338
NM_001001411.3(ZNF676):c.251G>C (p.Ser84Thr)
NM_001001411.3(ZNF676):c.277G>T (p.Val93Leu)
NM_001001411.3(ZNF676):c.292T>C (p.Tyr98His)
NM_001001411.3(ZNF676):c.356C>A (p.Ala119Glu) rs2513070970
NM_001001411.3(ZNF676):c.398T>G (p.Ile133Arg)
NM_001001411.3(ZNF676):c.406A>G (p.Thr136Ala) rs2023746006
NM_001001411.3(ZNF676):c.428G>A (p.Cys143Tyr)
NM_001001411.3(ZNF676):c.572A>G (p.His191Arg) rs1215098315
NM_001001411.3(ZNF676):c.586C>A (p.Pro196Thr) rs2023741036
NM_001001411.3(ZNF676):c.793G>T (p.Val265Phe)
NM_001001411.3(ZNF676):c.809C>T (p.Thr270Ile)
NM_001001411.3(ZNF676):c.87G>C (p.Glu29Asp) rs2513129001
NM_001001411.3(ZNF676):c.908A>G (p.His303Arg) rs765193548
NM_001001411.3(ZNF676):c.913G>C (p.Gly305Arg) rs767350295
NM_001001411.3(ZNF676):c.99G>A (p.Met33Ile)

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