ClinVar Miner

List of variants in gene CTNNB1 reported as likely pathogenic for adrenal cortex neoplasm

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP
NM_001904.3(CTNNB1):c.100G>C (p.Gly34Arg) rs121913399
NM_001904.3(CTNNB1):c.101G>A (p.Gly34Glu) rs28931589
NM_001904.3(CTNNB1):c.101G>C (p.Gly34Ala) rs28931589
NM_001904.3(CTNNB1):c.101G>T (p.Gly34Val) rs28931589
NM_001904.3(CTNNB1):c.121A>G (p.Thr41Ala) rs121913412
NM_001904.3(CTNNB1):c.122C>A (p.Thr41Asn) rs121913413
NM_001904.3(CTNNB1):c.122C>T (p.Thr41Ile) rs121913413
NM_001904.3(CTNNB1):c.133T>C (p.Ser45Pro) rs121913407
NM_001904.3(CTNNB1):c.134C>A (p.Ser45Tyr) rs121913409
NM_001904.3(CTNNB1):c.134C>G (p.Ser45Cys) rs121913409
NM_001904.3(CTNNB1):c.134C>T (p.Ser45Phe) rs121913409

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