ClinVar Miner

Variants in gene TRIOBP with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 47
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HGVS dbSNP gnomAD frequency
NM_001039141.3(TRIOBP):c.1866T>C (p.Asp622=) rs6000868 0.05844
NM_001039141.3(TRIOBP):c.2234G>A (p.Arg745Lys) rs150690007 0.00672
NM_001039141.3(TRIOBP):c.1158C>T (p.Asp386=) rs116964444 0.00651
NM_001039141.3(TRIOBP):c.6472+10C>T rs369182277 0.00575
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.2724G>A (p.Ser908=) rs12160218 0.00303
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.5886A>G (p.Pro1962=) rs372220018 0.00171
NM_001039141.3(TRIOBP):c.3954C>T (p.Ser1318=) rs200990219 0.00157
NM_001039141.3(TRIOBP):c.4728T>C (p.Arg1576=) rs112874177 0.00143
NM_001039141.3(TRIOBP):c.6741G>A (p.Leu2247=) rs375013523 0.00137
NM_001039141.3(TRIOBP):c.4139A>G (p.Glu1380Gly) rs202059880 0.00133
NM_001039141.3(TRIOBP):c.5058C>G (p.Pro1686=) rs113459040 0.00123
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.1690A>G (p.Thr564Ala) rs777175618 0.00097
NM_001039141.3(TRIOBP):c.363C>A (p.Ser121=) rs201843208 0.00091
NM_001039141.3(TRIOBP):c.1132C>T (p.Pro378Ser) rs183024099 0.00087
NM_001039141.3(TRIOBP):c.1226G>A (p.Arg409Gln) rs148874577 0.00085
NM_001039141.3(TRIOBP):c.2201C>T (p.Ser734Phe) rs199794705 0.00069
NM_001039141.3(TRIOBP):c.2992G>A (p.Ala998Thr) rs200019928 0.00064
NM_001039141.3(TRIOBP):c.5767G>A (p.Ala1923Thr) rs150947392 0.00064
NM_001039141.3(TRIOBP):c.6414G>A (p.Gln2138=) rs369245613 0.00063
NM_001039141.3(TRIOBP):c.4077T>C (p.Pro1359=) rs139074745 0.00058
NM_001039141.3(TRIOBP):c.965C>T (p.Ala322Val) rs145588841 0.00053
NM_001039141.3(TRIOBP):c.497G>C (p.Ser166Thr) rs540459171 0.00049
NM_001039141.3(TRIOBP):c.6362C>T (p.Ser2121Leu) rs201724032 0.00036
NM_001039141.3(TRIOBP):c.4329A>G (p.Leu1443=) rs547759535 0.00035
NM_001039141.3(TRIOBP):c.5764C>T (p.Arg1922Trp) rs183941928 0.00032
NM_001039141.3(TRIOBP):c.4510A>G (p.Arg1504Gly) rs374991119 0.00022
NM_001039141.3(TRIOBP):c.4726C>T (p.Arg1576Cys) rs200113910 0.00020
NM_001039141.3(TRIOBP):c.114+16A>G rs117561671 0.00015
NM_001039141.3(TRIOBP):c.964G>T (p.Ala322Ser) rs201693690 0.00014
NM_001039141.3(TRIOBP):c.6575+14G>A rs577534147 0.00002
NM_001039141.3(TRIOBP):c.1263T>C (p.Asn421=) rs566207993
NM_001039141.3(TRIOBP):c.1591G>A (p.Ala531Thr) rs201112075
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+14_6472+15insC rs546389039
NM_001039141.3(TRIOBP):c.6472+14_6472+15insT rs546389039
NM_001039141.3(TRIOBP):c.6472+15_6472+16insC rs149021782
NM_001039141.3(TRIOBP):c.6936+13G>T rs727503529

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