"PreventionGenetics, part of Exact Sciences"[submitter] AND "TRAF3IP2" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 761641	NM_147686.4(TRAF3IP2):c.1221T>C (p.Tyr407=)	TRAF3IP2, TRAF3IP2-AS1	Single nucleotide variant (synonymous variant)	TRAF3IP2-related condition +1 more	GLikely benign
Select item 541102	NM_147686.4(TRAF3IP2):c.1184A>G (p.Asn395Ser)	TRAF3IP2-AS1, TRAF3IP2 (N395S +1 more)	Single nucleotide variant (missense variant)	TRAF3IP2-related condition +1 more	GLikely benign
Select item 769688	NM_147686.4(TRAF3IP2):c.1020C>T (p.His340=)	TRAF3IP2, TRAF3IP2-AS1	Single nucleotide variant (synonymous variant)	TRAF3IP2-related condition +1 more	GBenign/Likely benign
Select item 541101	NM_147686.4(TRAF3IP2):c.957C>A (p.Ser319Arg)	TRAF3IP2, TRAF3IP2-AS1 (S319R +1 more)	Single nucleotide variant (missense variant)	TRAF3IP2-related condition +1 more	GBenign
Select item 1106655	NM_147686.4(TRAF3IP2):c.813C>T (p.Pro271=)	TRAF3IP2-AS1, LOC114803478 +1 more	Single nucleotide variant (synonymous variant)	TRAF3IP2-related condition +1 more	GLikely benign
Select item 720205	NM_147686.4(TRAF3IP2):c.232C>G (p.Arg78Gly)	LOC114803478, TRAF3IP2 +1 more (R78G +1 more)	Single nucleotide variant (missense variant)	TRAF3IP2-related condition +1 more	GConflicting classifications of pathogenicity

ClinVar