List of variants in gene CTNNB1, LOC126806658 studied for Carcinoma of esophagus

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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.97T>A (p.Ser33Thr)	rs1057519886
NM_001904.4(CTNNB1):c.97T>C (p.Ser33Pro)	rs1057519886
NM_001904.4(CTNNB1):c.97T>G (p.Ser33Ala)	rs1057519886
NM_001904.4(CTNNB1):c.98C>A (p.Ser33Tyr)	rs121913400
NM_001904.4(CTNNB1):c.98C>G (p.Ser33Cys)	rs121913400
NM_001904.4(CTNNB1):c.98C>T (p.Ser33Phe)	rs121913400

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