List of variants in gene ZNF292 reported as uncertain significance for not provided

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: 123

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HGVS	dbSNP	gnomAD frequency
NM_015021.3(ZNF292):c.4046G>A (p.Arg1349Gln)	rs572597069	0.00003
NM_015021.3(ZNF292):c.2632A>G (p.Ile878Val)	rs1256311307	0.00002
NM_015021.3(ZNF292):c.6809G>A (p.Arg2270Gln)	rs1256417163	0.00002
NM_015021.3(ZNF292):c.1178A>T (p.Glu393Val)	rs957020155	0.00001
NM_015021.3(ZNF292):c.7423A>G (p.Lys2475Glu)	rs753298856	0.00001
NM_015021.3(ZNF292):c.7870C>G (p.His2624Asp)	rs551397183	0.00001
NM_015021.3(ZNF292):c.7930C>A (p.Pro2644Thr)	rs1775603873	0.00001
NM_015021.3(ZNF292):c.8139dup (p.Ile2714fs)	rs769701632	0.00001
NM_015021.3(ZNF292):c.1034G>C (p.Gly345Ala)	rs2482283134
NM_015021.3(ZNF292):c.1066G>A (p.Ala356Thr)	rs976963327
NM_015021.3(ZNF292):c.1094C>G (p.Thr365Ser)
NM_015021.3(ZNF292):c.1160G>A (p.Arg387His)	rs2482284460
NM_015021.3(ZNF292):c.1223TGT[1] (p.Leu409del)
NM_015021.3(ZNF292):c.1232A>G (p.Asn411Ser)
NM_015021.3(ZNF292):c.1270A>G (p.Ile424Val)	rs1775128550
NM_015021.3(ZNF292):c.1388A>C (p.Glu463Ala)	rs1775133764
NM_015021.3(ZNF292):c.1436A>G (p.Tyr479Cys)
NM_015021.3(ZNF292):c.1673G>A (p.Arg558Gln)	rs2482290215
NM_015021.3(ZNF292):c.1675C>T (p.His559Tyr)
NM_015021.3(ZNF292):c.1715C>T (p.Pro572Leu)	rs2127857888
NM_015021.3(ZNF292):c.1760A>C (p.His587Pro)	rs2127858055
NM_015021.3(ZNF292):c.1805C>G (p.Ala602Gly)
NM_015021.3(ZNF292):c.189G>C (p.Glu63Asp)	rs2482017974
NM_015021.3(ZNF292):c.1946A>G (p.Asn649Ser)	rs1160342281
NM_015021.3(ZNF292):c.1957G>T (p.Gly653Cys)
NM_015021.3(ZNF292):c.2036A>G (p.Asn679Ser)
NM_015021.3(ZNF292):c.2059T>A (p.Phe687Ile)	rs200991861
NM_015021.3(ZNF292):c.2150T>C (p.Met717Thr)
NM_015021.3(ZNF292):c.2204C>A (p.Thr735Asn)	rs2482297353
NM_015021.3(ZNF292):c.2342G>A (p.Cys781Tyr)
NM_015021.3(ZNF292):c.2462A>C (p.Gln821Pro)
NM_015021.3(ZNF292):c.2614C>T (p.Leu872Phe)
NM_015021.3(ZNF292):c.2689_2690delinsCA (p.Ser897Gln)
NM_015021.3(ZNF292):c.2743G>A (p.Gly915Arg)
NM_015021.3(ZNF292):c.2758G>C (p.Gly920Arg)	rs1775214847
NM_015021.3(ZNF292):c.2780CTC[1] (p.Pro928del)	rs575913628
NM_015021.3(ZNF292):c.2971_2973del (p.Glu991del)	rs2482307101
NM_015021.3(ZNF292):c.3120A>T (p.Gln1040His)	rs369021831
NM_015021.3(ZNF292):c.3260C>T (p.Pro1087Leu)	rs1775252925
NM_015021.3(ZNF292):c.3418C>G (p.Gln1140Glu)	rs2482313479
NM_015021.3(ZNF292):c.3549G>C (p.Gln1183His)
NM_015021.3(ZNF292):c.3568C>G (p.Pro1190Ala)	rs1775274397
NM_015021.3(ZNF292):c.3797C>T (p.Pro1266Leu)	rs2482318800
NM_015021.3(ZNF292):c.3831A>G (p.Ser1277=)
NM_015021.3(ZNF292):c.3962C>T (p.Pro1321Leu)	rs1775299810
NM_015021.3(ZNF292):c.4012T>G (p.Ser1338Ala)
NM_015021.3(ZNF292):c.4033_4035del (p.Lys1345del)	rs2482322258
NM_015021.3(ZNF292):c.4094A>C (p.Lys1365Thr)
NM_015021.3(ZNF292):c.4300T>A (p.Leu1434Met)	rs2482325784
NM_015021.3(ZNF292):c.436T>G (p.Cys146Gly)	rs2482036334
NM_015021.3(ZNF292):c.4378A>G (p.Asn1460Asp)	rs2482326923
NM_015021.3(ZNF292):c.4433T>G (p.Phe1478Cys)
NM_015021.3(ZNF292):c.4493G>T (p.Gly1498Val)
NM_015021.3(ZNF292):c.4505C>G (p.Thr1502Arg)
NM_015021.3(ZNF292):c.4531C>T (p.His1511Tyr)	rs2482329454
NM_015021.3(ZNF292):c.463G>A (p.Ala155Thr)	rs2482036628
NM_015021.3(ZNF292):c.4723T>G (p.Leu1575Val)
NM_015021.3(ZNF292):c.4746T>A (p.Asn1582Lys)
NM_015021.3(ZNF292):c.4771A>G (p.Asn1591Asp)
NM_015021.3(ZNF292):c.4789C>G (p.Gln1597Glu)
NM_015021.3(ZNF292):c.4917T>C (p.Ile1639=)	rs2482335466
NM_015021.3(ZNF292):c.4937A>G (p.Asn1646Ser)	rs2482335733
NM_015021.3(ZNF292):c.4943T>G (p.Val1648Gly)	rs2482335833
NM_015021.3(ZNF292):c.5030G>T (p.Cys1677Phe)
NM_015021.3(ZNF292):c.5046G>C (p.Leu1682Phe)	rs2127868090
NM_015021.3(ZNF292):c.5080A>C (p.Asn1694His)
NM_015021.3(ZNF292):c.5083A>C (p.Asn1695His)	rs2482337555
NM_015021.3(ZNF292):c.5185C>G (p.Gln1729Glu)
NM_015021.3(ZNF292):c.5251G>A (p.Val1751Ile)	rs2482339657
NM_015021.3(ZNF292):c.5270A>C (p.Lys1757Thr)	rs2482339935
NM_015021.3(ZNF292):c.5285T>C (p.Ile1762Thr)
NM_015021.3(ZNF292):c.5298G>C (p.Met1766Ile)
NM_015021.3(ZNF292):c.5367A>G (p.Ile1789Met)	rs2482341179
NM_015021.3(ZNF292):c.5440T>G (p.Ser1814Ala)
NM_015021.3(ZNF292):c.554C>T (p.Ala185Val)
NM_015021.3(ZNF292):c.5578T>C (p.Cys1860Arg)
NM_015021.3(ZNF292):c.5675_5678del (p.Ile1892fs)	rs1775426161
NM_015021.3(ZNF292):c.5760T>G (p.Phe1920Leu)	rs2482347539
NM_015021.3(ZNF292):c.5775A>C (p.Lys1925Asn)
NM_015021.3(ZNF292):c.5820T>G (p.Asn1940Lys)
NM_015021.3(ZNF292):c.583A>G (p.Arg195Gly)	rs2482124878
NM_015021.3(ZNF292):c.5858C>T (p.Thr1953Ile)	rs2127870701
NM_015021.3(ZNF292):c.5939T>G (p.Val1980Gly)	rs2127870871
NM_015021.3(ZNF292):c.6055T>C (p.Ser2019Pro)	rs769408368
NM_015021.3(ZNF292):c.6145del (p.Ser2049fs)	rs764995318
NM_015021.3(ZNF292):c.6175G>A (p.Val2059Met)
NM_015021.3(ZNF292):c.6248G>A (p.Arg2083Lys)	rs539510683
NM_015021.3(ZNF292):c.6254A>G (p.His2085Arg)	rs1397964000
NM_015021.3(ZNF292):c.6268G>C (p.Glu2090Gln)
NM_015021.3(ZNF292):c.6292G>T (p.Val2098Phe)
NM_015021.3(ZNF292):c.6296C>A (p.Ser2099Tyr)	rs768826330
NM_015021.3(ZNF292):c.6305T>A (p.Leu2102His)
NM_015021.3(ZNF292):c.6329C>T (p.Pro2110Leu)	rs2127872385
NM_015021.3(ZNF292):c.6527T>C (p.Val2176Ala)	rs1395658492
NM_015021.3(ZNF292):c.6806C>T (p.Thr2269Ile)	rs2482362536
NM_015021.3(ZNF292):c.685C>G (p.Gln229Glu)
NM_015021.3(ZNF292):c.6878G>T (p.Arg2293Ile)	rs2482363293
NM_015021.3(ZNF292):c.6884dup (p.Leu2295fs)	rs2127873897
NM_015021.3(ZNF292):c.6998C>A (p.Thr2333Asn)
NM_015021.3(ZNF292):c.7001A>T (p.Lys2334Ile)	rs890621431
NM_015021.3(ZNF292):c.7018_7023del (p.Asn2340_Leu2341del)	rs2482365296
NM_015021.3(ZNF292):c.7021T>A (p.Leu2341Ile)	rs1270393952
NM_015021.3(ZNF292):c.7032_7034del (p.Lys2344del)	rs1216193398
NM_015021.3(ZNF292):c.7043T>C (p.Ile2348Thr)	rs3812131
NM_015021.3(ZNF292):c.7044T>G (p.Ile2348Met)
NM_015021.3(ZNF292):c.7168A>G (p.Ile2390Val)
NM_015021.3(ZNF292):c.7192A>G (p.Thr2398Ala)	rs2482367741
NM_015021.3(ZNF292):c.7378G>C (p.Asp2460His)
NM_015021.3(ZNF292):c.742-3T>G	rs2482207163
NM_015021.3(ZNF292):c.7507C>T (p.Gln2503Ter)	rs1131691860
NM_015021.3(ZNF292):c.7531A>G (p.Ser2511Gly)
NM_015021.3(ZNF292):c.7614T>G (p.Asn2538Lys)
NM_015021.3(ZNF292):c.7754C>A (p.Ser2585Tyr)
NM_015021.3(ZNF292):c.7832A>G (p.Asp2611Gly)
NM_015021.3(ZNF292):c.7849A>G (p.Thr2617Ala)	rs2482376797
NM_015021.3(ZNF292):c.7874C>A (p.Ser2625Ter)	rs2127877426
NM_015021.3(ZNF292):c.8102C>G (p.Ser2701Ter)
NM_015021.3(ZNF292):c.8152A>G (p.Thr2718Ala)	rs1775618174
NM_015021.3(ZNF292):c.824T>C (p.Leu275Ser)	rs2482208154
NM_015021.3(ZNF292):c.855A>T (p.Gln285His)
NM_015021.3(ZNF292):c.872G>T (p.Cys291Phe)
NM_015021.3(ZNF292):c.923C>T (p.Pro308Leu)
NM_015021.3(ZNF292):c.976A>C (p.Thr326Pro)

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