ClinVar Miner

List of variants in gene TMPO reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_001032283.3(TMPO):c.565+939C>T rs113427737 0.01520
NM_001032283.3(TMPO):c.565+107A>T rs114920815 0.01250
NM_001032283.3(TMPO):c.*115A>C rs1802615 0.01118
NM_001032283.3(TMPO):c.*105C>T rs7966614 0.01011
NM_001032283.3(TMPO):c.879+191T>A rs147140222 0.00862
NM_001032283.3(TMPO):c.565+2661A>T rs113105753 0.00686
NM_001032283.3(TMPO):c.565+99A>C rs187564154 0.00530
NM_001032283.3(TMPO):c.280-188A>G rs73382597 0.00494
NM_001032283.3(TMPO):c.406+304G>A rs112520632 0.00494
NM_001032283.3(TMPO):c.990+74T>G rs564477164 0.00443
NM_001032283.3(TMPO):c.565+2744C>G rs114931887 0.00359
NM_001032283.3(TMPO):c.990+166G>C rs553103093 0.00307
NM_001032283.3(TMPO):c.407-219C>T rs189604487 0.00284
NM_001032283.3(TMPO):c.406+296G>C rs182833695 0.00145
NM_001032283.3(TMPO):c.565+1696C>T rs141443652 0.00142
NM_001032283.3(TMPO):c.565+2224A>G rs34983516 0.00098
NM_001032283.3(TMPO):c.1119G>A (p.Arg373=) rs144913822 0.00083
NM_001032283.3(TMPO):c.1296A>G (p.Gln432=) rs61744201 0.00076
NM_001032283.3(TMPO):c.350A>G (p.Asn117Ser) rs141387097 0.00068
NM_001032283.3(TMPO):c.565+2149C>T rs34150443 0.00064
NM_001032283.3(TMPO):c.565+2368G>A rs138295270 0.00058
NM_001032283.3(TMPO):c.654G>A (p.Glu218=) rs138298699 0.00054
NM_001032283.3(TMPO):c.565+1750C>G rs142981381 0.00038
NM_001032283.3(TMPO):c.565+1493A>G rs141347778 0.00031
NM_001032283.3(TMPO):c.565+1748T>A rs138388686 0.00025
NM_001032283.3(TMPO):c.-11A>C rs377404642 0.00019
NM_001032283.3(TMPO):c.534T>C (p.Asn178=) rs200016687 0.00016
NM_001032283.3(TMPO):c.565+1298G>A rs370939324 0.00016
NM_001032283.3(TMPO):c.565+2376C>T rs202035749 0.00015
NM_001032283.3(TMPO):c.565+1469A>G rs147812883 0.00014
NM_001032283.3(TMPO):c.565+1413A>G rs57670957 0.00005
NM_001032283.3(TMPO):c.565+1277G>A rs766680788 0.00004
NM_001032283.3(TMPO):c.565+1304T>A rs142500409 0.00004
NM_001032283.3(TMPO):c.565+1574G>A rs756784841 0.00004
NM_001032283.3(TMPO):c.565+1958G>T rs143845319 0.00004
NM_001032283.3(TMPO):c.330A>G (p.Leu110=) rs776054749 0.00003
NM_001032283.3(TMPO):c.565+1982A>C rs766190912 0.00003
NM_001032283.3(TMPO):c.777G>A (p.Arg259=) rs200238614 0.00003
NM_001032283.3(TMPO):c.*7T>C rs557563034 0.00002
NM_001032283.3(TMPO):c.153G>A (p.Pro51=) rs755323971 0.00002
NM_001032283.3(TMPO):c.565+1356C>T rs139512723 0.00002
NM_001032283.3(TMPO):c.565+2150A>G rs200856956 0.00002
NM_001032283.3(TMPO):c.108G>T (p.Val36=) rs532884813 0.00001
NM_001032283.3(TMPO):c.565+1499A>G rs776923796 0.00001
NM_001032283.3(TMPO):c.565+1979T>C rs777452560 0.00001
NM_001032283.3(TMPO):c.565+1997G>A rs375056835 0.00001
NM_001032283.3(TMPO):c.1182T>C (p.Tyr394=) rs2121262613
NM_001032283.3(TMPO):c.357T>G (p.Asp119Glu) rs765524061
NM_001032283.3(TMPO):c.565+2135A>G rs1284474609
NM_001032283.3(TMPO):c.565+2450A>G rs267603733
NM_001032283.3(TMPO):c.990+66_990+67dup rs573744306
NM_001032283.3(TMPO):c.990+67dup rs573744306
NM_001032283.3(TMPO):c.991-12_991-11del rs759630477

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