List of variants in gene CTNNB1 reported as pathogenic by CeGaT Center for Human Genetics Tuebingen

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_001904.4(CTNNB1):c.2083del (p.Asp695fs)
NM_001904.4(CTNNB1):c.788del (p.Leu263fs)	rs2078159857
NM_001904.4(CTNNB1):c.876_882del (p.Phe293fs)	rs2078161525
NM_001904.4(CTNNB1):c.981_982del (p.Met328fs)	rs2078198486
NM_001904.4(CTNNB1):c.998dup (p.Tyr333Ter)	rs886041281

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