List of variants in gene CTNNA1 reported as likely pathogenic by Genomic Center, National Cancer Institute

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001903.5(CTNNA1):c.1479del (p.Lys493fs)	rs1762114658
NM_001903.5(CTNNA1):c.1559del (p.Leu520fs)	rs2150287805
NM_001903.5(CTNNA1):c.2213del (p.Asn738fs)	rs2150336916
NM_001903.5(CTNNA1):c.235del (p.Ile79fs)	rs2149656665

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