ClinVar Miner

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

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Gene type:
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Total variants: 58
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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.391G>A (p.Gly131Ser) rs144634857 0.00455
NM_001039141.3(TRIOBP):c.265C>G (p.Pro89Ala) rs199646135 0.00379
NM_001039141.3(TRIOBP):c.2105A>G (p.Gln702Arg) rs202079450 0.00304
NM_001039141.3(TRIOBP):c.584C>T (p.Thr195Ile) rs143157673 0.00258
NM_001039141.3(TRIOBP):c.2149C>G (p.Gln717Glu) rs186620158 0.00221
NM_001039141.3(TRIOBP):c.1225C>T (p.Arg409Trp) rs200333366 0.00151
NM_001039141.3(TRIOBP):c.4728T>C (p.Arg1576=) rs112874177 0.00143
NM_001039141.3(TRIOBP):c.4139A>G (p.Glu1380Gly) rs202059880 0.00133
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.4099C>T (p.Arg1367Trp) rs191589773 0.00097
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.3074G>A (p.Arg1025Gln) rs368593552 0.00020
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.1039C>T (p.Arg347Ter) rs118204026 0.00010
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.1193_1195del (p.Gln398del) rs55745992
NM_001039141.3(TRIOBP):c.1263T>C (p.Asn421=) rs566207993
NM_001039141.3(TRIOBP):c.1446C>A (p.Ala482=) rs1258642756
NM_001039141.3(TRIOBP):c.251_254+22del rs1555894574
NM_001039141.3(TRIOBP):c.3487_3533del (p.Pro1163fs) rs1569042640
NM_001039141.3(TRIOBP):c.3854_3855del (p.Arg1285fs) rs750744696
NM_001039141.3(TRIOBP):c.6472+13_6472+14insT rs541980281
NM_001039141.3(TRIOBP):c.6472+14G>T rs45503898
NM_001039141.3(TRIOBP):c.6472+15_6472+16insC rs149021782
NM_001039141.3(TRIOBP):c.6472+16G>C rs754782306
NM_001039141.3(TRIOBP):c.6472+19dup rs3833924
NM_001039141.3(TRIOBP):c.6957A>G (p.Gly2319=) rs1555901905
NM_001039141.3(TRIOBP):c.7066_7068del (p.Lys2356del) rs1283797116

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