"Ambry Genetics"[submitter] AND "LOC126805644"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3330718	NM_020765.3(UBR4):c.5401A>T (p.Asn1801Tyr)	LOC126805644, UBR4 (N1801Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205611	NM_020765.3(UBR4):c.5386C>T (p.Arg1796Trp)	LOC126805644, UBR4 (R1796W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544023	NM_020765.3(UBR4):c.5250G>T (p.Arg1750Ser)	LOC126805644, UBR4 (R1750S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607057	NM_020765.3(UBR4):c.5119G>A (p.Ala1707Thr)	LOC126805644, UBR4 (A1707T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326629	NM_020765.3(UBR4):c.5068G>A (p.Val1690Ile)	LOC126805644, UBR4 (V1690I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255226	NM_020765.3(UBR4):c.4978A>G (p.Lys1660Glu)	LOC126805644, UBR4 (K1660E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar