"Ambry Genetics"[submitter] AND "ZNF595"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3258837	NM_182524.4(ZNF595):c.277G>T (p.Asp93Tyr)	ZNF595 (D61Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2342302	NM_182524.4(ZNF595):c.295A>G (p.Ile99Val)	ZNF595 (I67V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2209402	NM_182524.4(ZNF595):c.301A>C (p.Lys101Gln)	ZNF595 (K101Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2490523	NM_182524.4(ZNF595):c.325G>A (p.Glu109Lys)	ZNF595 (E77K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2205848	NM_182524.4(ZNF595):c.362A>G (p.Asn121Ser)	ZNF595 (N121S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3258836	NM_182524.4(ZNF595):c.373G>A (p.Val125Met)	ZNF595 (V93M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2537494	NM_182524.4(ZNF595):c.388A>T (p.Asn130Tyr)	ZNF595 (N130Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2389957	NM_182524.4(ZNF595):c.493A>G (p.Ile165Val)	ZNF595 (I133V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar