List of variants in gene TRIOBP reported as uncertain significance 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: 33

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HGVS	dbSNP	gnomAD frequency
NM_001039141.3(TRIOBP):c.2149C>G (p.Gln717Glu)	rs186620158	0.00221
NM_001039141.3(TRIOBP):c.815C>A (p.Thr272Lys)	rs140901235	0.00119
NM_001039141.3(TRIOBP):c.3068C>T (p.Ala1023Val)	rs201681832	0.00116
NM_001039141.3(TRIOBP):c.634G>A (p.Gly212Ser)	rs201794404	0.00115
NM_001039141.3(TRIOBP):c.2811C>T (p.Ile937=)	rs115800799	0.00111
NM_001039141.3(TRIOBP):c.3309C>T (p.His1103=)	rs199594270	0.00082
NM_001039141.3(TRIOBP):c.5705A>C (p.Lys1902Thr)	rs138804394	0.00071
NM_001039141.3(TRIOBP):c.2201C>T (p.Ser734Phe)	rs199794705	0.00069
NM_001039141.3(TRIOBP):c.6771G>A (p.Gln2257=)	rs200793989	0.00058
NM_001039141.3(TRIOBP):c.3219G>A (p.Ala1073=)	rs374759271	0.00053
NM_001039141.3(TRIOBP):c.4783C>T (p.Arg1595Cys)	rs201117318	0.00034
NM_001039141.3(TRIOBP):c.5853G>A (p.Leu1951=)	rs55821172	0.00030
NM_001039141.3(TRIOBP):c.483G>A (p.Glu161=)	rs368119524	0.00028
NM_001039141.3(TRIOBP):c.1283C>G (p.Pro428Arg)	rs372134073	0.00023
NM_001039141.3(TRIOBP):c.6360C>T (p.Ser2120=)	rs375936342	0.00021
NM_001039141.3(TRIOBP):c.3774C>T (p.Pro1258=)	rs377749969	0.00020
NM_001039141.3(TRIOBP):c.1874G>C (p.Arg625Thr)	rs886043820	0.00017
NM_001039141.3(TRIOBP):c.3084G>A (p.Ser1028=)	rs763012991	0.00007
NM_001039141.3(TRIOBP):c.2590C>T (p.Pro864Ser)	rs762514605	0.00005
NM_001039141.3(TRIOBP):c.446C>T (p.Ser149Leu)	rs769860248	0.00004
NM_001039141.3(TRIOBP):c.6123T>A (p.Asn2041Lys)	rs372525528	0.00004
NM_001039141.3(TRIOBP):c.1213T>C (p.Ser405Pro)	rs778139949	0.00003
NM_001039141.3(TRIOBP):c.3892C>T (p.Arg1298Cys)	rs370519121	0.00003
NM_001039141.3(TRIOBP):c.3944G>A (p.Arg1315His)	rs772997803	0.00002
NM_001039141.3(TRIOBP):c.6472+19_6472+20insA	rs397769084	0.00002
NM_001039141.3(TRIOBP):c.3429C>T (p.Ser1143=)	rs370721352	0.00001
NM_001039141.3(TRIOBP):c.6723G>C (p.Leu2241=)	rs756330364	0.00001
NM_001039141.3(TRIOBP):c.118C>T (p.Leu40Phe)	rs1555894553
NM_001039141.3(TRIOBP):c.1446C>A (p.Ala482=)	rs1258642756
NM_001039141.3(TRIOBP):c.6472+14G>T	rs45503898
NM_001039141.3(TRIOBP):c.6472+16G>C	rs754782306
NM_001039141.3(TRIOBP):c.6957A>G (p.Gly2319=)	rs1555901905
NM_001039141.3(TRIOBP):c.7066_7068del (p.Lys2356del)	rs1283797116

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