"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "TUBB8"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1176540	NM_177987.3(TUBB8):c.1301_1327del (p.Glu434_Glu442del)	TUBB8	Deletion (inframe_deletion)	not provided	GLikely benign
Select item 2578610	NM_177987.3(TUBB8):c.867T>C (p.Leu289=)	TUBB8	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1879128	NM_177987.3(TUBB8):c.762C>G (p.Ala254=)	TUBB8	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2640263	NM_177987.3(TUBB8):c.414C>T (p.Ser138=)	TUBB8	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3025247	NM_177987.3(TUBB8):c.291C>A (p.Ala97=)	TUBB8	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2498456	NM_177987.3(TUBB8):c.124C>G (p.Leu42Val)	TUBB8 (L42V)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 775282	NM_177987.3(TUBB8):c.9G>A (p.Glu3=)	TUBB8	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign

ClinVar