List of variants in gene CTNNA3 reported by Blueprint Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_013266.4(CTNNA3):c.2573T>C (p.Leu858Ser)	rs41313840	0.00028
NM_013266.4(CTNNA3):c.457G>C (p.Ala153Pro)	rs147116577	0.00015
NM_013266.4(CTNNA3):c.377G>A (p.Arg126His)	rs730880071	0.00005
NM_013266.4(CTNNA3):c.2500C>T (p.Arg834Ter)	rs202196166	0.00004
NM_013266.4(CTNNA3):c.35A>T (p.Asp12Val)	rs730880069	0.00004
NM_013266.4(CTNNA3):c.232C>T (p.Gln78Ter)	rs201306690	0.00003
NM_013266.4(CTNNA3):c.622C>T (p.Arg208Ter)	rs755323657	0.00002
NM_013266.4(CTNNA3):c.1073C>A (p.Thr358Asn)	rs751471841	0.00001
NM_013266.4(CTNNA3):c.1031C>T (p.Ser344Leu)	rs730880072
NM_013266.4(CTNNA3):c.2053A>G (p.Ser685Gly)	rs199697536
NM_013266.4(CTNNA3):c.242C>T (p.Thr81Ile)	rs730880070
NM_013266.4(CTNNA3):c.2430del (p.Ala811fs)	rs869025379
NM_013266.4(CTNNA3):c.2571del (p.Pro857_Leu858insTer)	rs587782935
NM_013266.4(CTNNA3):c.2588del (p.Lys863fs)	rs730880073

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