List of variants in gene TRIOBP reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_001039141.3(TRIOBP):c.4129T>C (p.Trp1377Arg)	rs8140958	0.96815
NM_001039141.3(TRIOBP):c.3975G>A (p.Gln1325=)	rs7284476	0.35508
NM_001039141.3(TRIOBP):c.6498C>T (p.Tyr2166=)	rs4821708	0.24140
NM_001039141.3(TRIOBP):c.4116G>T (p.Glu1372Asp)	rs8140207	0.23344
NM_001039141.3(TRIOBP):c.-14C>G	rs12484441	0.18268
NM_001039141.3(TRIOBP):c.6324+226A>G	rs57799594	0.10409
NM_001039141.3(TRIOBP):c.4178C>T (p.Pro1393Leu)	rs28450766	0.00750
NM_001039141.3(TRIOBP):c.6899T>C (p.Val2300Ala)	rs61737841	0.00748
NM_001039141.3(TRIOBP):c.4165C>A (p.Leu1389Ile)	rs144175566	0.00642
NM_001039141.3(TRIOBP):c.7032G>A (p.Glu2344=)	rs61737839	0.00637
NM_001039141.3(TRIOBP):c.6571C>T (p.His2191Tyr)	rs61729063	0.00635
NM_001039141.3(TRIOBP):c.6806A>G (p.Asn2269Ser)	rs61729060	0.00634
NM_001039141.3(TRIOBP):c.6472+10C>T	rs369182277	0.00575
NM_001039141.3(TRIOBP):c.504C>A (p.Asp168Glu)	rs116448422	0.00567
NM_001039141.3(TRIOBP):c.5052G>T (p.Thr1684=)	rs41283241	0.00539
NM_001039141.3(TRIOBP):c.6135C>T (p.Pro2045=)	rs11546529	0.00524
NM_001039141.3(TRIOBP):c.6736G>A (p.Glu2246Lys)	rs138139146	0.00483
NM_001039141.3(TRIOBP):c.391G>A (p.Gly131Ser)	rs144634857	0.00455
NM_001039141.3(TRIOBP):c.265C>G (p.Pro89Ala)	rs199646135	0.00379
NM_001039141.3(TRIOBP):c.4643C>T (p.Pro1548Leu)	rs78894866	0.00357
NM_001039141.3(TRIOBP):c.584C>T (p.Thr195Ile)	rs143157673	0.00258
NM_001039141.3(TRIOBP):c.4031G>A (p.Arg1344Gln)	rs34066624	0.00238
NM_001039141.3(TRIOBP):c.4333A>G (p.Arg1445Gly)	rs199640717	0.00225
NM_001039141.3(TRIOBP):c.5767G>A (p.Ala1923Thr)	rs150947392	0.00064
NM_001039141.3(TRIOBP):c.4077T>C (p.Pro1359=)	rs139074745	0.00058
NM_001039141.3(TRIOBP):c.6362C>T (p.Ser2121Leu)	rs201724032	0.00036
NM_001039141.3(TRIOBP):c.4484A>T (p.Glu1495Val)	rs183455182	0.00026
NM_001039141.3(TRIOBP):c.4726C>T (p.Arg1576Cys)	rs200113910	0.00020
NM_001039141.3(TRIOBP):c.6455C>T (p.Thr2152Met)	rs534215753	0.00006
NM_001039141.3(TRIOBP):c.6272G>C (p.Ser2091Thr)	rs78758968

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