ClinVar Miner

List of variants in gene TMPO studied for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 76
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HGVS dbSNP gnomAD frequency
NM_001032283.3(TMPO):c.565+2214C>G rs17459334 0.06758
NM_001032283.3(TMPO):c.565+1369C>G rs35969221 0.03471
NM_001032283.3(TMPO):c.565+1665A>G rs11838270 0.02179
NM_001032283.3(TMPO):c.991-4T>C rs112475937 0.01905
NM_001032283.3(TMPO):c.565+1296T>G rs35645287 0.01895
NM_001032283.3(TMPO):c.565+1132T>G rs35998138 0.01742
NM_001032283.3(TMPO):c.565+1853G>C rs35761089 0.01735
NM_001032283.3(TMPO):c.565+2051T>A rs12316677 0.01280
NM_001032283.3(TMPO):c.565+1890T>G rs80325832 0.01253
NM_001032283.3(TMPO):c.565+1344G>C rs114939776 0.01252
NM_001032283.3(TMPO):c.859G>C (p.Ala287Pro) rs7133258 0.00977
NM_001032283.3(TMPO):c.565+2487C>T rs17028450 0.00576
NM_001032283.3(TMPO):c.*1A>G rs1058300 0.00324
NM_001032283.3(TMPO):c.565+1240G>A rs139700737 0.00284
NM_001032283.3(TMPO):c.565+1728G>C rs145703021 0.00188
NM_001032283.3(TMPO):c.87C>T (p.Ala29=) rs114074541 0.00153
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.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.565+1105C>T rs138790561 0.00038
NM_001032283.3(TMPO):c.565+1848G>A rs34301677 0.00037
NM_001032283.3(TMPO):c.565+1493A>G rs141347778 0.00031
NM_001032283.3(TMPO):c.-11A>C rs377404642 0.00019
NM_001032283.3(TMPO):c.806G>A (p.Arg269His) rs142891873 0.00017
NM_001032283.3(TMPO):c.534T>C (p.Asn178=) rs200016687 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+1641A>G rs143232629 0.00011
NM_001032283.3(TMPO):c.565+2387G>A rs201034441 0.00008
NM_001032283.3(TMPO):c.565+1328G>T rs369208265 0.00006
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.614G>A (p.Arg205Lys) rs727504952 0.00004
NM_001032283.3(TMPO):c.1174C>T (p.Pro392Ser) rs727504622 0.00003
NM_001032283.3(TMPO):c.330A>G (p.Leu110=) rs776054749 0.00003
NM_001032283.3(TMPO):c.565+1301A>G rs375249647 0.00003
NM_001032283.3(TMPO):c.565+1917A>G rs727505217 0.00003
NM_001032283.3(TMPO):c.153G>A (p.Pro51=) rs755323971 0.00002
NM_001032283.3(TMPO):c.565+1232C>T rs369897433 0.00002
NM_001032283.3(TMPO):c.565+1356C>T rs139512723 0.00002
NM_001032283.3(TMPO):c.70A>C (p.Asn24His) rs727505279 0.00002
NM_001032283.3(TMPO):c.108G>T (p.Val36=) rs532884813 0.00001
NM_001032283.3(TMPO):c.565+1137G>A rs375903462 0.00001
NM_001032283.3(TMPO):c.565+1275A>G rs763320036 0.00001
NM_001032283.3(TMPO):c.565+1499A>G rs776923796 0.00001
NM_001032283.3(TMPO):c.565+1606C>T rs727505047 0.00001
NM_001032283.3(TMPO):c.565+1907A>G rs372248802 0.00001
NM_001032283.3(TMPO):c.565+1997G>A rs375056835 0.00001
NM_001032283.3(TMPO):c.565+2178G>A rs1343917914 0.00001
NM_001032283.3(TMPO):c.72T>C (p.Asn24=) rs201960762 0.00001
NM_001032283.3(TMPO):c.1079+5dup rs34449077
NM_001032283.3(TMPO):c.190G>A (p.Asp64Asn) rs1462361337
NM_001032283.3(TMPO):c.19G>C (p.Asp7His)
NM_001032283.3(TMPO):c.357T>G (p.Asp119Glu) rs765524061
NM_001032283.3(TMPO):c.396T>A (p.Gly132=) rs397516844
NM_001032283.3(TMPO):c.565+1127C>T rs777779709
NM_001032283.3(TMPO):c.565+1242A>G
NM_001032283.3(TMPO):c.565+1548A>G rs779658294
NM_001032283.3(TMPO):c.565+1777G>C
NM_001032283.3(TMPO):c.565+1782G>A rs763388598
NM_001032283.3(TMPO):c.565+1819A>G rs1479099731
NM_001032283.3(TMPO):c.565+1983del
NM_001032283.3(TMPO):c.565+2042A>C rs397516842
NM_001032283.3(TMPO):c.565+2135A>G rs1284474609
NM_001032283.3(TMPO):c.565+2138T>G
NM_001032283.3(TMPO):c.565+2296C>T rs397516843
NM_001032283.3(TMPO):c.565+2450A>G rs267603733
NM_001032283.3(TMPO):c.565+2461_565+2463del rs727503491
NM_001032283.3(TMPO):c.663+13T>G rs727504798
NM_001032283.3(TMPO):c.681A>G (p.Gly227=) rs727504733
NM_001032283.3(TMPO):c.77C>T (p.Thr26Met) rs397516494
NM_001032283.3(TMPO):c.991-14_991-11del rs397516495

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