List of variants in gene TRAPPC9 reported as benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_001160372.4(TRAPPC9):c.207T>C (p.Gly69=)	rs3735801	0.55959
NM_001160372.4(TRAPPC9):c.288T>C (p.Phe96=)	rs3735802	0.55845
NM_001160372.4(TRAPPC9):c.411C>T (p.Asn137=)	rs3735803	0.45974
NM_001160372.4(TRAPPC9):c.1692C>T (p.Asn564=)	rs12549048	0.22639
NM_001160372.4(TRAPPC9):c.2292C>T (p.Gly764=)	rs11166965	0.10684
NM_001160372.4(TRAPPC9):c.2431+7G>A	rs11166964	0.10663
NM_001160372.4(TRAPPC9):c.2799= (p.Gly933=)	rs2614718	0.08065
NM_001160372.4(TRAPPC9):c.2742C>T (p.Thr914=)	rs28710457	0.01086
NM_001160372.4(TRAPPC9):c.1869C>T (p.Ser623=)	rs117685875	0.01001
NM_001160372.4(TRAPPC9):c.3249C>T (p.Phe1083=)	rs112551069	0.00501
NM_001160372.4(TRAPPC9):c.2871G>A (p.Lys957=)	rs188700138	0.00045
NM_031466.8(TRAPPC9):c.-129_-109dup	rs367682297

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