List of variants in gene combination CTNNB1, LOC126806658 reported as pathogenic for embryonal neoplasm

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001904.4(CTNNB1):c.101G>T (p.Gly34Val)	rs28931589
NM_001904.4(CTNNB1):c.121A>G (p.Thr41Ala)	rs121913412
NM_001904.4(CTNNB1):c.283C>T (p.Arg95Ter)	rs775104326
NM_001904.4(CTNNB1):c.94G>T (p.Asp32Tyr)	rs28931588
NM_001904.4(CTNNB1):c.98C>T (p.Ser33Phe)	rs121913400

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