List of variants in gene CTNNA1 reported as likely benign by Fulgent Genetics, Fulgent Genetics

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.1899+18A>G	rs562041100	0.00058
NM_001903.5(CTNNA1):c.1782C>T (p.Ala594=)	rs142503438	0.00044
NM_001903.5(CTNNA1):c.2714G>A (p.Ser905Asn)	rs756360361	0.00006
NM_001903.5(CTNNA1):c.2442C>T (p.Ser814=)	rs143248909	0.00001
NM_001903.5(CTNNA1):c.588+4_588+5del	rs147724289

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