ClinVar Miner

List of variants in gene CTNNA3 reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_013266.4(CTNNA3):c.959C>T (p.Thr320Met)	rs139460414	0.00004
NM_013266.4(CTNNA3):c.2400+5G>A	rs2492642999

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