ClinVar Miner

List of variants in gene ZNF292 reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 18
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HGVS dbSNP gnomAD frequency
NM_015021.3(ZNF292):c.5520T>C (p.Ile1840=) rs373138423 0.00002
NM_015021.3(ZNF292):c.5630C>T (p.Thr1877Ile) rs1209095419 0.00002
NM_015021.3(ZNF292):c.1424A>G (p.Asp475Gly) rs1457087238 0.00001
NM_015021.3(ZNF292):c.2723C>T (p.Ser908Phe) rs1269690704 0.00001
NM_015021.3(ZNF292):c.3767A>T (p.Asp1256Val) rs753893386 0.00001
NM_015021.3(ZNF292):c.4726C>A (p.Leu1576Ile) rs752249653 0.00001
NM_015021.3(ZNF292):c.7264A>G (p.Asn2422Asp) rs756541832 0.00001
NM_015021.3(ZNF292):c.7346A>T (p.Lys2449Ile) rs950343147 0.00001
NM_015021.3(ZNF292):c.1142A>G (p.Asp381Gly)
NM_015021.3(ZNF292):c.269C>G (p.Pro90Arg) rs1327633366
NM_015021.3(ZNF292):c.2974C>G (p.Gln992Glu)
NM_015021.3(ZNF292):c.3131C>T (p.Pro1044Leu)
NM_015021.3(ZNF292):c.3491C>T (p.Ser1164Leu)
NM_015021.3(ZNF292):c.6079G>T (p.Ala2027Ser)
NM_015021.3(ZNF292):c.7003C>T (p.Arg2335Ter) rs1168689294
NM_015021.3(ZNF292):c.722A>G (p.Asn241Ser) rs2482126121
NM_015021.3(ZNF292):c.7614T>A (p.Asn2538Lys) rs778061441
NM_015021.3(ZNF292):c.7629_7633del (p.Lys2544fs) rs2482373985

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