List of variants in gene CTNNA1 reported as uncertain significance 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001903.5(CTNNA1):c.339T>A (p.Asp113Glu)	rs773771416	0.00001
NM_001903.5(CTNNA1):c.1229A>G (p.Asn410Ser)	rs2150032599
NM_001903.5(CTNNA1):c.1392del (p.Ile465fs)	rs2150233636
NM_001903.5(CTNNA1):c.1597A>G (p.Lys533Glu)	rs2150288180
NM_001903.5(CTNNA1):c.163T>C (p.Ser55Pro)	rs1755329623
NM_001903.5(CTNNA1):c.1645del (p.Ala549fs)	rs2150288925
NM_001903.5(CTNNA1):c.1715T>C (p.Val572Ala)	rs2150289732
NM_001903.5(CTNNA1):c.1944del (p.Phe648fs)	rs2150324882
NM_001903.5(CTNNA1):c.2047A>G (p.Lys683Glu)	rs2150334086
NM_001903.5(CTNNA1):c.2470A>G (p.Asn824Asp)	rs2150358511
NM_001903.5(CTNNA1):c.2665A>G (p.Lys889Glu)	rs1766015674

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