List of variants in gene TRAPPC9 reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_001160372.4(TRAPPC9):c.7G>A (p.Val3Ile)	rs76033442	0.00489
NM_001160372.4(TRAPPC9):c.263C>T (p.Ser88Leu)	rs139631202	0.00072
NM_001160372.4(TRAPPC9):c.2671A>C (p.Thr891Pro)	rs562249191	0.00066
NM_001160372.4(TRAPPC9):c.1019C>T (p.Ala340Val)	rs143778652	0.00056
NM_001160372.4(TRAPPC9):c.3175G>A (p.Ala1059Thr)	rs150200902	0.00056
NM_001160372.4(TRAPPC9):c.853C>T (p.Arg285Trp)	rs141441030	0.00045
NM_001160372.4(TRAPPC9):c.140G>A (p.Arg47Gln)	rs147182402	0.00024
NM_001160372.4(TRAPPC9):c.2882C>T (p.Ala961Val)	rs769398594	0.00010
NM_001160372.4(TRAPPC9):c.136G>A (p.Val46Met)	rs201233141	0.00009
NM_031466.8(TRAPPC9):c.-73G>C	rs767996463	0.00005
NM_001160372.4(TRAPPC9):c.3013C>A (p.Gln1005Lys)	rs913893905	0.00003
NM_001160372.4(TRAPPC9):c.1129C>T (p.Arg377Ter)	rs267607136	0.00001
NM_001160372.4(TRAPPC9):c.3217C>T (p.His1073Tyr)	rs1459705932	0.00001
NM_001160372.4(TRAPPC9):c.3364G>A (p.Glu1122Lys)	rs767963216	0.00001

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