ClinVar Miner

List of variants in gene TBX3 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_005996.4(TBX3):c.*245C>T rs77971713 0.02102
NM_005996.4(TBX3):c.777C>T (p.Ile259=) rs34627348 0.01205
NM_005996.4(TBX3):c.1710+110T>C rs74932638 0.01012
NM_005996.4(TBX3):c.1094A>G (p.His365Arg) rs141004177 0.00869
NM_005996.4(TBX3):c.804+298T>C rs74679747 0.00706
NM_005996.4(TBX3):c.390-281del rs59159218 0.00666
NM_005996.4(TBX3):c.61C>T (p.Leu21=) rs142592809 0.00648
NM_005996.4(TBX3):c.658-557C>T rs76431560 0.00597
NM_005996.4(TBX3):c.*12A>T rs150286184 0.00354
NM_005996.4(TBX3):c.-251G>A rs9805019 0.00290
NM_005996.4(TBX3):c.1236G>T (p.Ser412=) rs62640916 0.00282
NM_005996.4(TBX3):c.1271C>T (p.Ser424Phe) rs1450439762 0.00001
NM_005996.4(TBX3):c.-895TC[11] rs57078153
NM_005996.4(TBX3):c.-895TC[15] rs57078153
NM_005996.4(TBX3):c.-895TC[17] rs57078153
NM_005996.4(TBX3):c.1711-137_1711-135del rs55865934
NM_005996.4(TBX3):c.1711-146C>A rs11067230
NM_005996.4(TBX3):c.1711-153_1711-152dup rs3830417
NM_005996.4(TBX3):c.658-148G>T rs7134236
NM_005996.4(TBX3):c.881+14_881+17del rs139956231

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