"PreventionGenetics, part of Exact Sciences"[submitter] AND "UBE3B"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 703032	NM_130466.4(UBE3B):c.219A>C (p.Ala73=)	UBE3B	Single nucleotide variant (synonymous variant)	UBE3B-related disorder +1 more	GBenign
Select item 2174513	NM_130466.4(UBE3B):c.441G>A (p.Gln147=)	UBE3B	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3052911	NM_130466.4(UBE3B):c.631-490C>T	UBE3B	Single nucleotide variant (synonymous variant +1 more)	UBE3B-related disorder	GLikely benign
Select item 1599500	NM_130466.4(UBE3B):c.838T>C (p.Ser280Pro)	UBE3B (S280P)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 703034	NM_130466.4(UBE3B):c.1282+9C>T	UBE3B	Single nucleotide variant (intron variant)	UBE3B-related disorder +1 more	GBenign
Select item 2085176	NM_130466.4(UBE3B):c.2034G>A (p.Pro678=)	UBE3B	Single nucleotide variant (synonymous variant)	UBE3B-related disorder +1 more	GLikely benign
Select item 2725820	NM_130466.4(UBE3B):c.2379C>T (p.Asp793=)	UBE3B	Single nucleotide variant (synonymous variant)	UBE3B-related disorder +1 more	GLikely benign
Select item 702103	NM_130466.4(UBE3B):c.2430C>T (p.Ser810=)	UBE3B	Single nucleotide variant (synonymous variant)	UBE3B-related disorder +1 more	GBenign/Likely benign
Select item 3049427	NM_130466.4(UBE3B):c.2502+9G>A	UBE3B	Single nucleotide variant (intron variant)	UBE3B-related disorder	GLikely benign

ClinVar