Variants in gene TUBA1A with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_006009.4(TUBA1A):c.288A>G (p.Lys96=)	rs1056875	0.45696
NM_006009.4(TUBA1A):c.1008G>A (p.Lys336=)	rs11829764	0.00853
NM_006009.4(TUBA1A):c.786T>C (p.Tyr262=)	rs762008241	0.00096
NM_006009.4(TUBA1A):c.1044C>T (p.Pro348=)	rs144574983	0.00085
NM_006009.4(TUBA1A):c.226+10C>T	rs199717430	0.00078
NM_006009.4(TUBA1A):c.4-7C>T	rs560491477	0.00053
NM_006009.4(TUBA1A):c.390G>C (p.Thr130=)	rs1143559	0.00018
NM_006009.4(TUBA1A):c.1203A>G (p.Lys401=)	rs1065724	0.00002

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