List of variants in gene CTNNA1 reported as 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001903.5(CTNNA1):c.1045del (p.Ser349fs)	rs2149786068
NM_001903.5(CTNNA1):c.1526_1527insC (p.Asp509_Asp510insTer)	rs1762133912
NM_001903.5(CTNNA1):c.2043del (p.Ala682fs)	rs2150334022
NM_001903.5(CTNNA1):c.2600del (p.Lys867fs)	rs2150359552
NM_001903.5(CTNNA1):c.297del (p.Lys99fs)	rs2149656983

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