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

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3330563	NM_001012989.1(UBE2NL):c.35C>T	UBE2NL	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2515445	NM_001012989.3(UBE2NL):c.112G>A (p.Val38Ile)	UBE2NL (V38I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2537785	NM_001012989.3(UBE2NL):c.136T>G (p.Ser46Ala)	UBE2NL (S46A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2248666	NM_001012989.3(UBE2NL):c.235C>T (p.Pro79Ser)	UBE2NL (P79S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3185537	NM_001012989.3(UBE2NL):c.263G>A (p.Ser88Asn)	UBE2NL (S88N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458570	NM_001012989.3(UBE2NL):c.350A>G (p.Asn117Ser)	UBE2NL (N117S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2330325	NM_001012989.3(UBE2NL):c.353C>T (p.Pro118Leu)	UBE2NL (P118L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3330564	NM_001012989.1(UBE2NL):c.430T>C	UBE2NL	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2216670	NM_001012989.3(UBE2NL):c.455G>T (p.Ser152Ile)	UBE2NL (S152I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance