List of variants in gene TUBA1A reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_006009.4(TUBA1A):c.3+103C>T	rs35896524	0.03762
NM_006009.4(TUBA1A):c.*211A>G	rs140121590	0.00985
NM_006009.4(TUBA1A):c.376-149G>A	rs138835855	0.00810
NM_006009.4(TUBA1A):c.226+10C>T	rs199717430	0.00078
NM_006009.4(TUBA1A):c.227-17C>G	rs367632910	0.00030
NM_006009.4(TUBA1A):c.4-4A>G	rs1280504729	0.00003
NM_006009.4(TUBA1A):c.1227T>G (p.Val409=)	rs766135902	0.00001
NM_006009.4(TUBA1A):c.*1del (p.Ter452=)	rs781483247
NM_006009.4(TUBA1A):c.1230G>T (p.Gly410=)	rs772809398
NM_006009.4(TUBA1A):c.1257A>G (p.Ser419=)	rs865953916
NM_006009.4(TUBA1A):c.273A>G (p.Gln91=)	rs765483435
NM_006009.4(TUBA1A):c.3+157CGC[5]	rs560742601

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.