List of variants in gene CTNNA1 reported as benign by Ambry 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: 27

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HGVS	dbSNP	gnomAD frequency
NM_001903.5(CTNNA1):c.2220G>A (p.Ser740=)	rs1059110	0.32259
NM_001903.5(CTNNA1):c.540A>C (p.Leu180=)	rs11552054	0.02707
NM_001903.5(CTNNA1):c.2226C>G (p.Val742=)	rs11552052	0.02031
NM_001903.5(CTNNA1):c.546T>G (p.Pro182=)	rs28363395	0.01185
NM_001903.5(CTNNA1):c.1405C>T (p.Leu469=)	rs28363462	0.01143
NM_001903.5(CTNNA1):c.2343A>G (p.Gln781=)	rs75050399	0.00996
NM_001903.5(CTNNA1):c.1167C>T (p.His389=)	rs61736921	0.00225
NM_001903.5(CTNNA1):c.963C>T (p.Asp321=)	rs61736922	0.00073
NM_001903.5(CTNNA1):c.922C>T (p.Arg308Cys)	rs202131041	0.00027
NM_001903.5(CTNNA1):c.795C>G (p.Asp265Glu)	rs148239804	0.00013
NM_001903.5(CTNNA1):c.2434-5C>T	rs369052669	0.00010
NM_001903.5(CTNNA1):c.370A>G (p.Met124Val)	rs765587517	0.00009
NM_001903.5(CTNNA1):c.293G>A (p.Arg98Gln)	rs746832628	0.00008
NM_001903.5(CTNNA1):c.1352G>A (p.Arg451Gln)	rs773756164	0.00007
NM_001903.5(CTNNA1):c.1263A>G (p.Gln421=)	rs768184454	0.00006
NM_001903.5(CTNNA1):c.1304A>G (p.Asn435Ser)	rs752913534	0.00006
NM_001903.5(CTNNA1):c.228G>A (p.Gly76=)	rs776106481	0.00003
NM_001903.5(CTNNA1):c.1143+5T>C	rs766106863	0.00002
NM_001903.5(CTNNA1):c.1207G>A (p.Val403Ile)	rs760179421	0.00002
NM_001903.5(CTNNA1):c.839A>G (p.Tyr280Cys)	rs1427235870	0.00002
NM_001903.5(CTNNA1):c.897G>A (p.Glu299=)	rs141456038	0.00002
NM_001903.5(CTNNA1):c.2344C>T (p.Arg782Cys)	rs760684787	0.00001
NM_001903.5(CTNNA1):c.2434-4G>A	rs760241675	0.00001
NM_001903.5(CTNNA1):c.2692A>G (p.Ser898Gly)	rs776317664	0.00001
NM_001903.5(CTNNA1):c.483C>T (p.Ile161=)	rs955023956	0.00001
NM_001903.5(CTNNA1):c.710A>G (p.Tyr237Cys)	rs751967797	0.00001
NM_001903.5(CTNNA1):c.770A>G (p.Asn257Ser)	rs78627784

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