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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 789134	NM_005879.3(TRAIP):c.1269G>C (p.Arg423=)	TRAIP	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2181642	NM_005879.3(TRAIP):c.1260C>T (p.Leu420=)	TRAIP	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 748949	NM_005879.3(TRAIP):c.1067T>C (p.Ile356Thr)	TRAIP (I356T)	Single nucleotide variant (missense variant)	TRAIP-related disorder +1 more	GLikely benign
Select item 729558	NM_005879.3(TRAIP):c.1004G>T (p.Gly335Val)	TRAIP (G335V)	Single nucleotide variant (missense variant)	TRAIP-related disorder +1 more	GLikely benign
Select item 1913415	NM_005879.3(TRAIP):c.706-3T>C	TRAIP	Single nucleotide variant (intron variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2163298	NM_005879.3(TRAIP):c.624C>T (p.Tyr208=)	TRAIP	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 2788790	NM_005879.3(TRAIP):c.579G>A (p.Ala193=)	TRAIP	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 777775	NM_005879.3(TRAIP):c.99-9T>G	TRAIP	Single nucleotide variant (intron variant)	not provided +3 more	GBenign/Likely benign

ClinVar