ClinVar Miner

List of variants in gene ZNF292 reported as pathogenic

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Gene type:
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Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_015021.3(ZNF292):c.6823C>T (p.Arg2275Ter) rs1775506324 0.00001
NM_015021.3(ZNF292):c.1360C>T (p.Arg454Ter) rs1215967523
NM_015021.3(ZNF292):c.1414G>T (p.Glu472Ter) rs2482287354
NM_015021.3(ZNF292):c.1717del (p.Ile573fs) rs2482290757
NM_015021.3(ZNF292):c.2291dup (p.Tyr764Ter) rs2127859550
NM_015021.3(ZNF292):c.2311C>T (p.Arg771Ter) rs2482298524
NM_015021.3(ZNF292):c.2490_2494dup (p.Ser832fs) rs1775194783
NM_015021.3(ZNF292):c.2605dup (p.Arg869fs) rs2482302518
NM_015021.3(ZNF292):c.265C>T (p.Arg89Ter) rs865909396
NM_015021.3(ZNF292):c.2870_2871insT (p.Thr958fs)
NM_015021.3(ZNF292):c.3066_3069del (p.Glu1022fs) rs1135401779
NM_015021.3(ZNF292):c.3432_3436del (p.Asn1144fs) rs2482313661
NM_015021.3(ZNF292):c.3460_3463del (p.Val1154fs) rs1775264625
NM_015021.3(ZNF292):c.3611del (p.Leu1204fs) rs2127863644
NM_015021.3(ZNF292):c.3724del (p.Gln1242fs) rs1775285095
NM_015021.3(ZNF292):c.3915dup (p.Asn1306Ter)
NM_015021.3(ZNF292):c.3990del (p.Phe1330fs) rs2482321726
NM_015021.3(ZNF292):c.433del (p.Ser145fs) rs1772907934
NM_015021.3(ZNF292):c.4417dup (p.Ser1473fs) rs1775334064
NM_015021.3(ZNF292):c.4429_4432del (p.Asn1477fs)
NM_015021.3(ZNF292):c.4450C>T (p.Gln1484Ter) rs2482327974
NM_015021.3(ZNF292):c.4789C>T (p.Gln1597Ter)
NM_015021.3(ZNF292):c.4810del (p.Ser1604fs)
NM_015021.3(ZNF292):c.4837C>T (p.Gln1613Ter) rs2482334414
NM_015021.3(ZNF292):c.4839_4840del (p.Asn1614fs) rs2127867376
NM_015021.3(ZNF292):c.4897A>T (p.Lys1633Ter) rs1775368255
NM_015021.3(ZNF292):c.5112_5113del (p.Asn1705fs)
NM_015021.3(ZNF292):c.5233C>T (p.Gln1745Ter) rs2482339428
NM_015021.3(ZNF292):c.537del (p.Lys179_Val180insTer)
NM_015021.3(ZNF292):c.5759_5769del (p.Phe1920fs) rs2127870346
NM_015021.3(ZNF292):c.5950_5956del (p.Ile1984fs) rs2482349746
NM_015021.3(ZNF292):c.6001C>T (p.Arg2001Ter)
NM_015021.3(ZNF292):c.6038_6039del (p.Glu2013fs) rs879255403
NM_015021.3(ZNF292):c.6145dup (p.Ser2049fs) rs764995318
NM_015021.3(ZNF292):c.6160_6161del (p.Glu2054fs) rs1301328139
NM_015021.3(ZNF292):c.6224_6227del (p.Thr2075fs) rs2127871916
NM_015021.3(ZNF292):c.6239_6240del (p.Arg2080fs)
NM_015021.3(ZNF292):c.6266_6269del (p.Lys2089fs) rs2127872112
NM_015021.3(ZNF292):c.6279dup (p.Arg2094fs) rs1775468280
NM_015021.3(ZNF292):c.6280C>T (p.Arg2094Ter) rs2127872172
NM_015021.3(ZNF292):c.6517C>T (p.Arg2173Ter)
NM_015021.3(ZNF292):c.6541C>T (p.Arg2181Ter) rs377387515

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