Related gene-specific medical variations for Gene (Select 339327) - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3258628	NM_178544.5(ZNF546):c.1366C>G (p.Leu456Val)	LOC126862907, ZNF546 (L430V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258627	NM_178544.5(ZNF546):c.1477G>A (p.Gly493Ser)	LOC126862907, ZNF546 (G493S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258626	NM_178544.5(ZNF546):c.2083T>C (p.Cys695Arg)	LOC126862907, ZNF546 (C669R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258625	NM_178544.5(ZNF546):c.2138G>T (p.Arg713Ile)	LOC126862907, ZNF546 (R687I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258622	NM_178544.5(ZNF546):c.1486C>T (p.Pro496Ser)	LOC126862907, ZNF546 (P470S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196606	NM_178544.5(ZNF546):c.2096G>A (p.Gly699Glu)	LOC126862907, ZNF546 (G673E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196605	NM_178544.5(ZNF546):c.2080A>G (p.Ile694Val)	LOC126862907, ZNF546 (I694V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196604	NM_178544.5(ZNF546):c.2018C>T (p.Thr673Met)	LOC126862907, ZNF546 (T647M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196603	NM_178544.5(ZNF546):c.1916G>T (p.Cys639Phe)	LOC126862907, ZNF546 (C639F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196602	NM_178544.5(ZNF546):c.1895C>T (p.Thr632Ile)	LOC126862907, ZNF546 (T606I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196601	NM_178544.5(ZNF546):c.1832G>A (p.Cys611Tyr)	LOC126862907, ZNF546 (C585Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196600	NM_178544.5(ZNF546):c.1831T>C (p.Cys611Arg)	LOC126862907, ZNF546 (C585R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196599	NM_178544.5(ZNF546):c.1807C>A (p.His603Asn)	LOC126862907, ZNF546 (H577N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196598	NM_178544.5(ZNF546):c.1778G>A (p.Arg593His)	LOC126862907, ZNF546 (R567H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196597	NM_178544.5(ZNF546):c.1756T>C (p.Cys586Arg)	LOC126862907, ZNF546 (C586R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196596	NM_178544.5(ZNF546):c.1681G>T (p.Ala561Ser)	LOC126862907, ZNF546 (A561S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196595	NM_178544.5(ZNF546):c.1343A>G (p.Lys448Arg)	LOC126862907, ZNF546 (K448R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196593	NM_178544.5(ZNF546):c.1337G>A (p.Cys446Tyr)	LOC126862907, ZNF546 (C420Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196592	NM_178544.5(ZNF546):c.1328G>A (p.Cys443Tyr)	LOC126862907, ZNF546 (C443Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2649871	NM_178544.5(ZNF546):c.1974T>A (p.Ile658=)	LOC126862907, ZNF546	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2541075	NM_178544.5(ZNF546):c.1367T>C (p.Leu456Pro)	LOC126862907, ZNF546 (L456P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494114	NM_178544.5(ZNF546):c.1915T>G (p.Cys639Gly)	LOC126862907, ZNF546 (C613G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493991	NM_178544.5(ZNF546):c.1942C>T (p.Arg648Cys)	LOC126862907, ZNF546 (R622C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492013	NM_178544.5(ZNF546):c.2074C>G (p.Pro692Ala)	LOC126862907, ZNF546 (P666A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404122	NM_178544.5(ZNF546):c.1943G>A (p.Arg648His)	LOC126862907, ZNF546 (R648H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370725	NM_178544.5(ZNF546):c.1645T>C (p.Cys549Arg)	LOC126862907, ZNF546 (C549R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353715	NM_178544.5(ZNF546):c.2120G>A (p.Arg707Gln)	LOC126862907, ZNF546 (R681Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2340862	NM_178544.5(ZNF546):c.2198G>A (p.Arg733Gln)	LOC126862907, ZNF546 (R707Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323533	NM_178544.5(ZNF546):c.1718G>A (p.Arg573Gln)	LOC126862907, ZNF546 (R547Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308198	NM_178544.5(ZNF546):c.2447G>A (p.Arg816His)	LOC126862907, ZNF546 (R790H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205318	NM_178544.5(ZNF546):c.2458C>T (p.Leu820Phe)	LOC126862907, ZNF546 (L820F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 31