"Ambry Genetics"[submitter] AND "ZNF25"[gene] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3335248	NM_145011.4(ZNF25):c.1363G>C (p.Glu455Gln)	ZNF25 (E455Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194663	NM_145011.4(ZNF25):c.1327G>T (p.Ala443Ser)	ZNF25 (A407S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2548865	NM_145011.4(ZNF25):c.1193A>T (p.Tyr398Phe)	ZNF25 (Y402F +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2383452	NM_145011.4(ZNF25):c.1192T>C (p.Tyr398His)	ZNF25 (Y362H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194662	NM_145011.4(ZNF25):c.1126G>A (p.Gly376Ser)	ZNF25 (G340S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2232481	NM_145011.4(ZNF25):c.1109A>G (p.Tyr370Cys)	ZNF25 (Y334C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3335249	NM_145011.4(ZNF25):c.1099G>A (p.Glu367Lys)	ZNF25 (E366K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615065	NM_145011.4(ZNF25):c.1077A>T (p.Lys359Asn)	ZNF25 (K323N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2472740	NM_145011.4(ZNF25):c.1001G>A (p.Arg334Gln)	ZNF25 (R333Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194665	NM_145011.4(ZNF25):c.958A>G (p.Arg320Gly)	ZNF25 (R324G +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2246325	NM_145011.4(ZNF25):c.900C>G (p.His300Gln)	ZNF25 (H299Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2487493	NM_145011.4(ZNF25):c.800T>C (p.Phe267Ser)	ZNF25 (F231S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2373362	NM_145011.4(ZNF25):c.529A>G (p.Lys177Glu)	ZNF25 (K177E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392800	NM_145011.4(ZNF25):c.521A>G (p.Tyr174Cys)	ZNF25 (Y173C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366078	NM_145011.4(ZNF25):c.226C>T (p.Arg76Trp)	ZNF25 (R40W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194664	NM_145011.4(ZNF25):c.201G>T (p.Trp67Cys)	ZNF25 (W71C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2404570	NM_145011.4(ZNF25):c.175A>G (p.Lys59Glu)	ZNF25 (K23E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2317571	NM_145011.4(ZNF25):c.64T>C (p.Trp22Arg)	ZNF25 (W26R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2254629	NM_145011.4(ZNF25):c.14A>G (p.Gln5Arg)	ZNF25 (Q5R)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance