"Ambry Genetics"[submitter] AND "UBE2NL"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2515445	NM_001012989.3(UBE2NL):c.112G>A (p.Val38Ile)	UBE2NL (V38I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2537785	NM_001012989.3(UBE2NL):c.136T>G (p.Ser46Ala)	UBE2NL (S46A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2248666	NM_001012989.3(UBE2NL):c.235C>T (p.Pro79Ser)	UBE2NL (P79S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2458570	NM_001012989.3(UBE2NL):c.350A>G (p.Asn117Ser)	UBE2NL (N117S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2330325	NM_001012989.3(UBE2NL):c.353C>T (p.Pro118Leu)	UBE2NL (P118L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2216670	NM_001012989.3(UBE2NL):c.455G>T (p.Ser152Ile)	UBE2NL (S152I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

ClinVar