"PreventionGenetics, part of Exact Sciences"[submitter] AND "TRIM2"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3039148	NM_015271.5(TRIM2):c.-2C>T	TRIM2	Single nucleotide variant (5 prime UTR variant +1 more)	TRIM2-related disorder	GLikely benign
Select item 3033195	NM_015271.5(TRIM2):c.57C>T (p.Ala19=)	TRIM2	Single nucleotide variant (5 prime UTR variant +2 more)	TRIM2-related disorder	GLikely benign
Select item 2179388	NM_015271.5(TRIM2):c.117G>C (p.Val39=)	TRIM2	Single nucleotide variant (synonymous variant +2 more)	TRIM2-related disorder +1 more	GLikely benign
Select item 474610	NM_015271.5(TRIM2):c.122G>A (p.Arg41His)	TRIM2 (R14H +4 more)	Single nucleotide variant (missense variant +2 more)	not provided +2 more	GLikely benign
Select item 1141583	NM_015271.5(TRIM2):c.1296G>T (p.Leu432=)	TRIM2	Single nucleotide variant (synonymous variant)	TRIM2-related disorder +1 more	GLikely benign
Select item 704299	NM_015271.5(TRIM2):c.1671G>T (p.Pro557=)	TRIM2	Single nucleotide variant (synonymous variant)	TRIM2-related disorder +1 more	GLikely benign
Select item 711178	NM_015271.5(TRIM2):c.1698G>A (p.Val566=)	TRIM2	Single nucleotide variant (synonymous variant)	TRIM2-related disorder +2 more	GLikely benign

ClinVar