ClinVar Miner

List of variants in gene ZNF292 reported as uncertain significance for neurodevelopmental disorder

Included ClinVar conditions (779):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP gnomAD frequency
NM_015021.3(ZNF292):c.1408A>G (p.Ile470Val) rs1166797338 0.00001
NM_015021.3(ZNF292):c.1858G>T (p.Glu620Ter) rs1775159559
NM_015021.3(ZNF292):c.1897C>T (p.Arg633Ter) rs1775161294
NM_015021.3(ZNF292):c.1910del (p.Lys637fs) rs1775161900
NM_015021.3(ZNF292):c.2311C>T (p.Arg771Ter)
NM_015021.3(ZNF292):c.3053dup (p.Gln1019fs) rs1775236367
NM_015021.3(ZNF292):c.5374_5378del (p.Asn1792fs) rs1775403177
NM_015021.3(ZNF292):c.6578A>C (p.Tyr2193Ser) rs1554208945
NM_015021.3(ZNF292):c.6661_6664del (p.Leu2221fs) rs1775494843
NM_015021.3(ZNF292):c.6935dup (p.Ser2313fs) rs1775514251
NM_015021.3(ZNF292):c.6944_6946del (p.His2315del) rs2127874099
NM_015021.3(ZNF292):c.7062_7064del (p.Asn2354del) rs1775529808
NM_015021.3(ZNF292):c.7304_7308del (p.Val2435fs) rs1775548411

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