"PreventionGenetics, part of Exact Sciences"[submitter] AND "UBE3C"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3043379	NM_014671.3(UBE3C):c.459-8T>C	UBE3C	Single nucleotide variant (intron variant)	UBE3C-related disorder	GBenign
Select item 3050746	NM_014671.3(UBE3C):c.528G>C (p.Ser176=)	UBE3C	Single nucleotide variant (synonymous variant)	UBE3C-related disorder	GLikely benign
Select item 3056835	NM_014671.3(UBE3C):c.759G>A (p.Pro253=)	UBE3C	Single nucleotide variant (synonymous variant)	UBE3C-related disorder	GBenign
Select item 3042229	NM_014671.3(UBE3C):c.1143+9C>T	UBE3C	Single nucleotide variant (intron variant)	UBE3C-related disorder	GLikely benign
Select item 3059343	NM_014671.3(UBE3C):c.1503T>C (p.Tyr501=)	UBE3C	Single nucleotide variant (synonymous variant)	UBE3C-related disorder	GBenign
Select item 3051093	NM_014671.3(UBE3C):c.2230A>G (p.Asn744Asp)	UBE3C (N744D)	Single nucleotide variant (missense variant)	UBE3C-related disorder	GUncertain significance
Select item 3057827	NM_014671.3(UBE3C):c.2265C>T (p.His755=)	UBE3C	Single nucleotide variant (synonymous variant)	UBE3C-related disorder	GLikely benign
Select item 3052800	NM_014671.3(UBE3C):c.2754G>A (p.Ala918=)	UBE3C	Single nucleotide variant (synonymous variant)	UBE3C-related disorder	GLikely benign
Select item 3051489	NM_014671.3(UBE3C):c.2801A>C (p.Gln934Pro)	UBE3C (Q934P)	Single nucleotide variant (missense variant)	UBE3C-related disorder	GLikely benign

ClinVar