List of variants in gene combination CTNNB1, LOC126806658 reported as likely pathogenic for adrenal gland 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001904.4(CTNNB1):c.100G>C (p.Gly34Arg)	rs121913399
NM_001904.4(CTNNB1):c.101G>A (p.Gly34Glu)	rs28931589
NM_001904.4(CTNNB1):c.101G>C (p.Gly34Ala)	rs28931589
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.122C>A (p.Thr41Asn)	rs121913413
NM_001904.4(CTNNB1):c.122C>T (p.Thr41Ile)	rs121913413
NM_001904.4(CTNNB1):c.133T>C (p.Ser45Pro)	rs121913407
NM_001904.4(CTNNB1):c.134C>A (p.Ser45Tyr)	rs121913409
NM_001904.4(CTNNB1):c.134C>G (p.Ser45Cys)	rs121913409
NM_001904.4(CTNNB1):c.134C>T (p.Ser45Phe)	rs121913409

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