Variants in gene TUBB3 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_006086.4(TUBB3):c.921C>T (p.His307=)	rs147283850	0.00083
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.507C>T (p.Val169=)	rs373718068	0.00033
NM_006086.4(TUBB3):c.813C>T (p.Ala271=)	rs776465410	0.00002
NM_006086.4(TUBB3):c.1206C>T (p.Gly402=)	rs757192357	0.00001
NM_006086.4(TUBB3):c.1331C>T (p.Ser444Leu)	rs587784504	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

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