ClinVar Miner

List of variants in gene TUBB3 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_001197181.2(TUBB3):c.-160+1028C>T rs558683187 0.00347
NM_006086.4(TUBB3):c.921C>T (p.His307=) rs147283850 0.00083
NM_006086.4(TUBB3):c.166+12C>T rs374561094 0.00048
NM_006086.4(TUBB3):c.1287G>A (p.Thr429=) rs142238093 0.00046
NM_006086.4(TUBB3):c.357G>A (p.Val119=) rs34174718 0.00040
NM_006086.4(TUBB3):c.1197G>A (p.Thr399=) rs371418131 0.00021
NM_006086.4(TUBB3):c.855C>T (p.Thr285=) rs201682024 0.00013
NM_006086.4(TUBB3):c.278-7T>G rs199842533 0.00011
NM_006086.4(TUBB3):c.90C>T (p.Ile30=) rs369355135 0.00008
NM_006086.4(TUBB3):c.447G>A (p.Thr149=) rs371662941 0.00006
NM_006086.4(TUBB3):c.741C>T (p.Asn247=) rs138498822 0.00005
NM_006086.4(TUBB3):c.225T>C (p.Ser75=) rs199612798 0.00004
NM_006086.4(TUBB3):c.58-19del rs755935820 0.00004
NM_006086.4(TUBB3):c.882C>T (p.Phe294=) rs753163862 0.00004
NM_006086.4(TUBB3):c.936G>A (p.Thr312=) rs375770255 0.00002
NM_006086.4(TUBB3):c.1071G>A (p.Pro357=) rs754560439 0.00001
NM_006086.4(TUBB3):c.210C>T (p.Pro70=) rs754683361 0.00001
NM_006086.4(TUBB3):c.606C>T (p.Ile202=) rs576180572 0.00001
NM_006086.4(TUBB3):c.1113C>T (p.Ser371=) rs1057521639
NM_006086.4(TUBB3):c.167-21C>G rs72813449
NM_006086.4(TUBB3):c.278-175C>G rs75635769

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