"Ambry Genetics"[submitter] AND "ZNF346"[gene] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2333325	NM_012279.4(ZNF346):c.20C>G (p.Ala7Gly)	ZNF346 (A7G)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3335559	NM_012279.4(ZNF346):c.35C>T (p.Ala12Val)	ZNF346 (A12V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316599	NM_012279.4(ZNF346):c.64A>C (p.Ser22Arg)	ZNF346 (S22R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316600	NM_012279.4(ZNF346):c.65G>C (p.Ser22Thr)	ZNF346 (S22T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2410375	NM_012279.4(ZNF346):c.82G>A (p.Gly28Ser)	ZNF346 (G28S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2255360	NM_012279.4(ZNF346):c.98G>A (p.Gly33Glu)	ZNF346 (G33E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2226349	NM_012279.4(ZNF346):c.124C>T (p.Arg42Cys)	ZNF346 (R42C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550396	NM_012279.4(ZNF346):c.170A>G (p.Glu57Gly)	ZNF346 (E57G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2542486	NM_012279.4(ZNF346):c.189C>G (p.Ile63Met)	ZNF346 (I88M +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2404826	NM_012279.4(ZNF346):c.263A>G (p.Lys88Arg)	ZNF346 (K88R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2469724	NM_012279.4(ZNF346):c.442G>A (p.Val148Met)	ZNF346 (V173M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3195314	NM_012279.4(ZNF346):c.481A>G (p.Asn161Asp)	ZNF346 (N161D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2611805	NM_012279.4(ZNF346):c.589C>T (p.Pro197Ser)	ZNF346 (P213S +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2615943	NM_012279.4(ZNF346):c.643A>G (p.Lys215Glu)	ZNF346 (K117E +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2560818	NM_012279.4(ZNF346):c.691A>G (p.Thr231Ala)	ZNF346 (T256A +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3195315	NM_012279.4(ZNF346):c.868A>G (p.Thr290Ala)	ZNF346 (N148S +7 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance