"PreventionGenetics, part of Exact Sciences"[submitter] AND "TUBB"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3052561	NM_178014.4(TUBB):c.58-567A>G	TUBB (H31R)	Single nucleotide variant (missense variant +1 more)	TUBB-related disorder	GLikely benign
Select item 1309522	NM_178014.4(TUBB):c.830G>A (p.Gly277Glu)	TUBB (G205E +3 more)	Single nucleotide variant (missense variant +1 more)	TUBB-related disorder +1 more	GUncertain significance