"Ambry Genetics"[submitter] AND "LOC130059836"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2616644	NM_001113525.2(ZNF276):c.86G>A (p.Arg29Gln)	LOC130059836, ZNF276 (R29Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2345237	NM_001113525.2(ZNF276):c.92G>C (p.Arg31Pro)	LOC130059836, ZNF276 (R31P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2356007	NM_001113525.2(ZNF276):c.106C>T (p.Leu36Phe)	LOC130059836, ZNF276 (L36F)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2512046	NM_001113525.2(ZNF276):c.119C>G (p.Pro40Arg)	LOC130059836, ZNF276 (P40R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3194825	NM_001113525.2(ZNF276):c.153G>C (p.Trp51Cys)	LOC130059836, ZNF276 (W51C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2349775	NM_001113525.2(ZNF276):c.154G>T (p.Gly52Cys)	LOC130059836, ZNF276 (G52C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3194826	NM_001113525.2(ZNF276):c.164G>C (p.Gly55Ala)	LOC130059836, ZNF276 (G55A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

ClinVar