List of variants in gene TUBB3 reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_006086.4(TUBB3):c.278-212T>C	rs4396536	0.99125
NM_006086.4(TUBB3):c.*78T>C	rs1135425	0.58969
NM_006086.4(TUBB3):c.58-185G>A	rs2302898	0.32058
NM_006086.4(TUBB3):c.58-235C>G	rs28521461	0.21058
NM_006086.4(TUBB3):c.58-49C>T	rs28593634	0.19243
NM_006086.4(TUBB3):c.58-22C>T	rs2302897	0.19080
NM_006086.4(TUBB3):c.58-331T>G	rs58336812	0.10240
NM_006086.4(TUBB3):c.*148G>A	rs12207	0.07118
NM_006086.4(TUBB3):c.278-242C>T	rs56923882	0.06024
NM_006086.4(TUBB3):c.277+58C>T	rs77681059	0.05710
NM_006086.4(TUBB3):c.277+8C>T	rs77191445	0.03997
NM_006086.4(TUBB3):c.277+198C>T	rs76149661	0.03990
NM_006086.4(TUBB3):c.1215G>A (p.Glu405=)	rs141064323	0.00809
NM_006086.4(TUBB3):c.702C>T (p.Ser234=)	rs147245174	0.00803
NM_006086.4(TUBB3):c.278-97G>C	rs528815633	0.00481
NM_006086.4(TUBB3):c.1317C>T (p.Asp439=)	rs75950334	0.00324
NM_006086.4(TUBB3):c.435C>T (p.Ser145=)	rs146421795	0.00153
NM_006086.4(TUBB3):c.189C>T (p.Ala63=)	rs146730216	0.00054
NM_006086.4(TUBB3):c.507C>T (p.Val169=)	rs373718068	0.00033
NM_006086.4(TUBB3):c.666C>T (p.Tyr222=)	rs61743676	0.00021
NM_006086.4(TUBB3):c.228C>T (p.Val76=)	rs185447857	0.00012
NM_006086.4(TUBB3):c.330G>A (p.Ala110=)	rs535819460	0.00003
NM_006086.4(TUBB3):c.1336G>A (p.Ala446Thr)	rs369454228	0.00001
NM_006086.4(TUBB3):c.*213C>T	rs190989681
NM_006086.4(TUBB3):c.167-5C>G	rs147928399
NM_006086.4(TUBB3):c.58-20dup	rs112388869
NM_006086.4(TUBB3):c.58-21C>G	rs78656983

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