"PreventionGenetics, part of Exact Sciences"[submitter] AND "TUBG1"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3053507	NM_001070.5(TUBG1):c.150C>T (p.Val50=)	TUBG1	Single nucleotide variant (synonymous variant)	TUBG1-related disorder	GLikely benign
Select item 3030876	NM_001070.5(TUBG1):c.183C>A (p.Ile61=)	TUBG1	Single nucleotide variant (synonymous variant)	TUBG1-related disorder	GLikely benign
Select item 3030533	NM_001070.5(TUBG1):c.252G>A (p.Lys84=)	TUBG1	Single nucleotide variant (synonymous variant)	TUBG1-related disorder	GLikely benign
Select item 3048983	NM_001070.5(TUBG1):c.264A>G (p.Pro88=)	TUBG1	Single nucleotide variant (synonymous variant)	TUBG1-related disorder	GLikely benign
Select item 735569	NM_001070.5(TUBG1):c.460T>C (p.Leu154=)	TUBG1	Single nucleotide variant (synonymous variant)	TUBG1-related disorder +1 more	GLikely benign
Select item 389498	NM_001070.5(TUBG1):c.1318C>T (p.Arg440Trp)	TUBG1 (R440W)	Single nucleotide variant (missense variant)	TUBG1-related disorder +2 more	GBenign/Likely benign

ClinVar