Variants in gene TUBA1A with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_006009.4(TUBA1A):c.1225G>A (p.Val409Ile)	rs1565626928
NM_006009.4(TUBA1A):c.362G>A (p.Arg121Gln)	rs2121246284
NM_006009.4(TUBA1A):c.427G>A (p.Gly143Arg)	rs1131691318
NM_006009.4(TUBA1A):c.449C>T (p.Thr150Ile)	rs1565627339
NM_006009.4(TUBA1A):c.518C>T (p.Pro173Leu)	rs1565627304
NM_006009.4(TUBA1A):c.521C>T (p.Ala174Val)	rs587784489
NM_006009.4(TUBA1A):c.53A>G (p.Asn18Ser)	rs1064795213
NM_006009.4(TUBA1A):c.640C>T (p.Arg214Cys)	rs886044568
NM_006009.4(TUBA1A):c.652G>A (p.Asp218Asn)	rs1057517858
NM_006009.4(TUBA1A):c.790C>G (p.Arg264Gly)	rs137853043
NM_006009.4(TUBA1A):c.791G>A (p.Arg264His)	rs886043627

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