List of variants in gene TRIOBP reported as benign by Eurofins NTD LLC (GA)

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001039141.3(TRIOBP):c.3899A>G (p.His1300Arg)	rs739138	0.58971
NM_001039141.3(TRIOBP):c.3885C>T (p.Ser1295=)	rs739137	0.35439
NM_001039141.3(TRIOBP):c.1740C>A (p.Ala580=)	rs79945262	0.01670
NM_001039141.3(TRIOBP):c.4178C>T (p.Pro1393Leu)	rs28450766	0.00750
NM_001039141.3(TRIOBP):c.1158C>T (p.Asp386=)	rs116964444	0.00651
NM_001039141.3(TRIOBP):c.504C>A (p.Asp168Glu)	rs116448422	0.00567
NM_001039141.3(TRIOBP):c.6736G>A (p.Glu2246Lys)	rs138139146	0.00483
NM_001039141.3(TRIOBP):c.265C>G (p.Pro89Ala)	rs199646135	0.00379
NM_001039141.3(TRIOBP):c.3074G>A (p.Arg1025Gln)	rs368593552	0.00020
NM_001039141.3(TRIOBP):c.1193_1195del (p.Gln398del)	rs55745992
NM_001039141.3(TRIOBP):c.6472+13_6472+14insT	rs541980281
NM_001039141.3(TRIOBP):c.6472+15_6472+16insC	rs149021782
NM_001039141.3(TRIOBP):c.6472+19dup	rs3833924

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