List of variants in gene TUBB3 reported as pathogenic by OMIM

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_006086.4(TUBB3):c.1162A>G (p.Met388Val)	rs878853279
NM_006086.4(TUBB3):c.1228G>A (p.Glu410Lys)	rs267607165
NM_006086.4(TUBB3):c.1249G>A (p.Asp417Asn)	rs267607164
NM_006086.4(TUBB3):c.1249G>C (p.Asp417His)	rs267607164
NM_006086.4(TUBB3):c.533C>T (p.Thr178Met)	rs747480526
NM_006086.4(TUBB3):c.613G>A (p.Glu205Lys)	rs878853257
NM_006086.4(TUBB3):c.784C>T (p.Arg262Cys)	rs267607162
NM_006086.4(TUBB3):c.904G>A (p.Ala302Thr)	rs267607163
NM_006086.4(TUBB3):c.905C>T (p.Ala302Val)	rs878853258
NM_006086.4(TUBB3):c.967A>G (p.Met323Val)	rs878853256

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