List of variants in gene CTNNB1 reported by Genetic Services Laboratory, University of Chicago

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001904.4(CTNNB1):c.2340C>T (p.Asp780=)	rs2293303	0.01246
NM_001904.4(CTNNB1):c.2320C>T (p.Leu774=)	rs4135386	0.00390
NM_001904.4(CTNNB1):c.1023C>T (p.Ser341=)	rs34343353	0.00154
NM_001904.4(CTNNB1):c.860A>G (p.Asn287Ser)	rs35288908	0.00086
NM_001904.4(CTNNB1):c.1155C>A (p.Leu385=)	rs74692094	0.00041
NM_001904.4(CTNNB1):c.1830C>T (p.Ile610=)	rs374923885	0.00023
NM_001904.4(CTNNB1):c.1785C>T (p.Thr595=)	rs587780325
NM_001904.4(CTNNB1):c.2042C>T (p.Ser681Phe)	rs772401455
NM_001904.4(CTNNB1):c.2079del (p.Ala694fs)	rs2125650519
NM_001904.4(CTNNB1):c.2182G>C (p.Ala728Pro)	rs797045504

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