ClinVar Miner

List of variants in gene ZNF292 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 77
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HGVS dbSNP gnomAD frequency
NM_015021.3(ZNF292):c.3177T>C (p.Asn1059=) rs143504993 0.00451
NM_015021.3(ZNF292):c.1206G>A (p.Ala402=) rs116277830 0.00373
NM_015021.3(ZNF292):c.7387A>G (p.Arg2463Gly) rs141403535 0.00368
NM_015021.3(ZNF292):c.7721T>C (p.Ile2574Thr) rs114321262 0.00368
NM_015021.3(ZNF292):c.4896G>A (p.Lys1632=) rs114815908 0.00367
NM_015021.3(ZNF292):c.4926C>T (p.Asn1642=) rs41273277 0.00341
NM_015021.3(ZNF292):c.6951G>A (p.Gly2317=) rs187534807 0.00316
NM_015021.3(ZNF292):c.3667C>G (p.Gln1223Glu) rs61739183 0.00220
NM_015021.3(ZNF292):c.5823A>G (p.Gln1941=) rs146654070 0.00211
NM_015021.3(ZNF292):c.7286G>A (p.Arg2429Gln) rs61747660 0.00207
NM_015021.3(ZNF292):c.4724T>C (p.Leu1575Ser) rs11753862 0.00170
NM_015021.3(ZNF292):c.3426T>A (p.Ala1142=) rs41273273 0.00155
NM_015021.3(ZNF292):c.3589G>C (p.Ala1197Pro) rs140831084 0.00117
NM_015021.3(ZNF292):c.871T>G (p.Cys291Gly) rs184839913 0.00103
NM_015021.3(ZNF292):c.4911A>G (p.Pro1637=) rs148546767 0.00094
NM_015021.3(ZNF292):c.5027C>T (p.Thr1676Ile) rs183279203 0.00080
NM_015021.3(ZNF292):c.2930C>T (p.Thr977Ile) rs143144210 0.00069
NM_015021.3(ZNF292):c.5974T>C (p.Ser1992Pro) rs200457425 0.00063
NM_015021.3(ZNF292):c.3190C>T (p.Pro1064Ser) rs201859341 0.00055
NM_015021.3(ZNF292):c.5330C>T (p.Ser1777Phe) rs41273279 0.00055
NM_015021.3(ZNF292):c.7268T>A (p.Leu2423His) rs202042334 0.00040
NM_015021.3(ZNF292):c.6302C>T (p.Ser2101Phe) rs200254331 0.00030
NM_015021.3(ZNF292):c.2112G>A (p.Gly704=) rs375509766 0.00029
NM_015021.3(ZNF292):c.4577C>T (p.Thr1526Met) rs200259538 0.00029
NM_015021.3(ZNF292):c.4658C>T (p.Thr1553Met) rs199744299 0.00024
NM_015021.3(ZNF292):c.5211A>G (p.Thr1737=) rs201719507 0.00015
NM_015021.3(ZNF292):c.2919A>G (p.Pro973=) rs372245966 0.00013
NM_015021.3(ZNF292):c.6378G>A (p.Thr2126=) rs201454729 0.00013
NM_015021.3(ZNF292):c.6265A>C (p.Lys2089Gln) rs201626407 0.00012
NM_015021.3(ZNF292):c.3602C>T (p.Thr1201Ile) rs780800206 0.00010
NM_015021.3(ZNF292):c.515A>G (p.Gln172Arg) rs375133485 0.00010
NM_015021.3(ZNF292):c.5432C>T (p.Pro1811Leu) rs202137359 0.00008
NM_015021.3(ZNF292):c.6281G>A (p.Arg2094Gln) rs746371148 0.00007
NM_015021.3(ZNF292):c.3051C>G (p.Thr1017=) rs748571596 0.00005
NM_015021.3(ZNF292):c.5889C>T (p.Asn1963=) rs554012118 0.00005
NM_015021.3(ZNF292):c.3807T>C (p.Ser1269=) rs769502246 0.00004
NM_015021.3(ZNF292):c.2052T>C (p.Pro684=) rs373848653 0.00003
NM_015021.3(ZNF292):c.4328A>G (p.Asn1443Ser) rs199698005 0.00003
NM_015021.3(ZNF292):c.4519G>A (p.Glu1507Lys) rs750773292 0.00003
NM_015021.3(ZNF292):c.4778G>C (p.Gly1593Ala) rs747743366 0.00003
NM_015021.3(ZNF292):c.5563A>G (p.Thr1855Ala) rs370204704 0.00003
NM_015021.3(ZNF292):c.6103A>G (p.Asn2035Asp) rs772144518 0.00003
NM_015021.3(ZNF292):c.7797T>C (p.Leu2599=) rs369582897 0.00003
NM_015021.3(ZNF292):c.7905T>A (p.Ala2635=) rs376443708 0.00003
NM_015021.3(ZNF292):c.1287C>T (p.Arg429=) rs376610075 0.00002
NM_015021.3(ZNF292):c.1626G>A (p.Gln542=) rs182042752 0.00001
NM_015021.3(ZNF292):c.6002G>A (p.Arg2001Gln) rs1256350761 0.00001
NM_015021.3(ZNF292):c.6029C>T (p.Ala2010Val) rs751384080 0.00001
NM_015021.3(ZNF292):c.6498A>G (p.Lys2166=) rs752830835 0.00001
NM_015021.3(ZNF292):c.7280T>G (p.Phe2427Cys) rs774642356 0.00001
NM_015021.3(ZNF292):c.834G>A (p.Ala278=) rs781382344 0.00001
NM_015021.3(ZNF292):c.1446G>C (p.Val482=)
NM_015021.3(ZNF292):c.168+13941G>T
NM_015021.3(ZNF292):c.2277T>G (p.Ala759=) rs2482298164
NM_015021.3(ZNF292):c.2500CCT[1] (p.Pro835del) rs766239064
NM_015021.3(ZNF292):c.2622A>G (p.Ser874=) rs1031100251
NM_015021.3(ZNF292):c.2727G>C (p.Glu909Asp)
NM_015021.3(ZNF292):c.2904A>G (p.Thr968=)
NM_015021.3(ZNF292):c.3235G>A (p.Asp1079Asn) rs377156350
NM_015021.3(ZNF292):c.3820C>G (p.Leu1274Val)
NM_015021.3(ZNF292):c.4045C>T (p.Arg1349Trp)
NM_015021.3(ZNF292):c.4407A>G (p.Thr1469=) rs41273275
NM_015021.3(ZNF292):c.4630A>G (p.Asn1544Asp) rs766154099
NM_015021.3(ZNF292):c.5422G>A (p.Asp1808Asn) rs556893194
NM_015021.3(ZNF292):c.5648T>C (p.Ile1883Thr)
NM_015021.3(ZNF292):c.5838C>G (p.Pro1946=) rs140100853
NM_015021.3(ZNF292):c.6214C>T (p.Leu2072Phe)
NM_015021.3(ZNF292):c.7149A>G (p.Val2383=) rs915235064
NM_015021.3(ZNF292):c.717A>G (p.Ser239=)
NM_015021.3(ZNF292):c.7185A>G (p.Ser2395=)
NM_015021.3(ZNF292):c.7293C>T (p.Cys2431=)
NM_015021.3(ZNF292):c.7498G>A (p.Val2500Ile) rs915267492
NM_015021.3(ZNF292):c.7537_7539del (p.Asp2513del) rs540701557
NM_015021.3(ZNF292):c.7659A>T (p.Ala2553=)
NM_015021.3(ZNF292):c.7845G>A (p.Pro2615=) rs777380559
NM_015021.3(ZNF292):c.849G>A (p.Gln283=)
NM_015021.3(ZNF292):c.957A>G (p.Gln319=) rs368623280

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