List of variants in gene CTNNB1, LOC126806658 studied for cervix disorder

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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001904.4(CTNNB1):c.109T>C (p.Ser37Pro)	rs121913228
NM_001904.4(CTNNB1):c.109T>G (p.Ser37Ala)	rs121913228
NM_001904.4(CTNNB1):c.110C>A (p.Ser37Tyr)	rs121913403
NM_001904.4(CTNNB1):c.110C>G (p.Ser37Cys)	rs121913403
NM_001904.4(CTNNB1):c.110C>T (p.Ser37Phe)	rs121913403
NM_001904.4(CTNNB1):c.94G>A (p.Asp32Asn)	rs28931588
NM_001904.4(CTNNB1):c.94G>C (p.Asp32His)	rs28931588
NM_001904.4(CTNNB1):c.94G>T (p.Asp32Tyr)	rs28931588
NM_001904.4(CTNNB1):c.95A>C (p.Asp32Ala)	rs121913396
NM_001904.4(CTNNB1):c.95A>G (p.Asp32Gly)	rs121913396
NM_001904.4(CTNNB1):c.95A>T (p.Asp32Val)	rs121913396

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