List of variants in gene TRAPPC9 reported as benign by Ambry Genetics

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: 18

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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.399T>C (p.Ala133=)	rs61739560	0.08885
NM_001160372.4(TRAPPC9):c.555G>A (p.Lys185=)	rs57593250	0.08881
NM_001160372.4(TRAPPC9):c.357G>A (p.Gly119=)	rs34457678	0.08878
NM_001160372.4(TRAPPC9):c.2799= (p.Gly933=)	rs2614718	0.08065
NM_001160372.4(TRAPPC9):c.3279+4C>T	rs79877357	0.02434
NM_001160372.4(TRAPPC9):c.1869C>T (p.Ser623=)	rs117685875	0.01001
NM_001160372.4(TRAPPC9):c.414C>T (p.Tyr138=)	rs115986561	0.00912
NM_001160372.4(TRAPPC9):c.2797G>A (p.Gly933Ser)	rs114949291	0.00641
NM_001160372.4(TRAPPC9):c.7G>A (p.Val3Ile)	rs76033442	0.00489
NM_001160372.4(TRAPPC9):c.2871G>A (p.Lys957=)	rs188700138	0.00045
NM_031466.8(TRAPPC9):c.-135A>G	rs148523016	0.00037
NM_001160372.4(TRAPPC9):c.3225C>T (p.Tyr1075=)	rs58740567
NM_031466.8(TRAPPC9):c.-129_-109dup	rs367682297

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