CN850169[trait identifier] AND "Illumina Laboratory Services, Illumina - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 421739	NM_001069.3(TUBB2A):c.292G>A (p.Gly98Arg)	TUBB2A (G98R +1 more)	Single nucleotide variant (missense variant)	Tubulinopathy +2 more	GPathogenic/Likely pathogenic
Select item 1195195	NM_178012.5(TUBB2B):c.1228G>A (p.Glu410Lys)	TUBB2B (E410K)	Single nucleotide variant (missense variant)	Tubulinopathy +1 more	GPathogenic/Likely pathogenic
Select item 3062041	NM_178012.5(TUBB2B):c.416T>C (p.Leu139Pro)	TUBB2B (L139P)	Single nucleotide variant (missense variant)	Tubulinopathy	GLikely pathogenic

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