List of variants in gene CTNNA1 reported as likely pathogenic for cancer or benign tumor

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001903.5(CTNNA1):c.105+1G>C	rs374313094
NM_001903.5(CTNNA1):c.1390-6_1392delinsA
NM_001903.5(CTNNA1):c.1479del (p.Lys493fs)	rs1762114658
NM_001903.5(CTNNA1):c.1559del (p.Leu520fs)	rs2150287805
NM_001903.5(CTNNA1):c.1899+1G>C	rs1580862601
NM_001903.5(CTNNA1):c.195_198del (p.Glu66fs)	rs869312766
NM_001903.5(CTNNA1):c.1991dup (p.Ala665fs)	rs1764809610
NM_001903.5(CTNNA1):c.1997del (p.Gly666fs)	rs1181915653
NM_001903.5(CTNNA1):c.2008dup (p.Arg670fs)
NM_001903.5(CTNNA1):c.2017_2018dup (p.Met673fs)
NM_001903.5(CTNNA1):c.2213del (p.Asn738fs)	rs2150336916
NM_001903.5(CTNNA1):c.235del (p.Ile79fs)	rs2149656665
NM_001903.5(CTNNA1):c.302-1G>A
NM_001903.5(CTNNA1):c.302-2A>G
NM_001903.5(CTNNA1):c.468+1G>T

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