List of variants in gene TUBB1 reported as likely pathogenic for not provided

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_030773.4(TUBB1):c.35del (p.Cys12fs)	rs773248042	0.00006
NM_030773.4(TUBB1):c.229C>T (p.Arg77Ter)	rs767380935
NM_030773.4(TUBB1):c.230G>A (p.Arg77Gln)	rs572988631
NM_030773.4(TUBB1):c.745G>C (p.Asp249His)	rs2091981798
NM_030773.4(TUBB1):c.779T>C (p.Phe260Ser)	rs1057517996
NM_030773.4(TUBB1):c.838C>T (p.Gln280Ter)

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