ClinVar Miner

List of variants in gene TMPO reported as benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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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.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+1105C>T rs138790561 0.00038
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.565+1469A>G rs147812883 0.00014
NM_001032283.3(TMPO):c.565+2387G>A rs201034441 0.00008
NM_001032283.3(TMPO):c.565+1304T>A rs142500409 0.00004
NM_001032283.3(TMPO):c.1079+5dup rs34449077
NM_001032283.3(TMPO):c.396T>A (p.Gly132=) rs397516844

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