"Ambry Genetics"[submitter] AND "ZNF667"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2299075	NM_001321356.2(ZNF667):c.1808A>G (p.Asn603Ser)	ZNF667 (N603S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197587	NM_001321356.2(ZNF667):c.1651G>A (p.Gly551Arg)	ZNF667 (G551R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197586	NM_001321356.2(ZNF667):c.1510T>C (p.Cys504Arg)	ZNF667 (C504R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233278	NM_001321356.2(ZNF667):c.1292A>G (p.Lys431Arg)	ZNF667 (K431R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544223	NM_001321356.2(ZNF667):c.1256A>G (p.Glu419Gly)	ZNF667 (E362G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389948	NM_001321356.2(ZNF667):c.1190G>A (p.Arg397Gln)	ZNF667 (R340Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345822	NM_001321356.2(ZNF667):c.935C>T (p.Ala312Val)	ZNF667 (A255V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3197590	NM_001321356.2(ZNF667):c.919A>G (p.Lys307Glu)	ZNF667 (K250E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197589	NM_001321356.2(ZNF667):c.775G>A (p.Gly259Arg)	ZNF667 (G202R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197588	NM_001321356.2(ZNF667):c.245G>A (p.Arg82Gln)	LOC126862940, ZNF667 (R82Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2588291	NM_001321356.2(ZNF667):c.244C>T (p.Arg82Trp)	LOC126862940, ZNF667 (R82W)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2390843	NM_001321356.2(ZNF667):c.173G>A (p.Arg58Gln)	ZNF667 (R58Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3197585	NM_001321356.2(ZNF667):c.142C>T (p.Arg48Trp)	ZNF667 (R48W)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance