ClinVar Miner

List of variants in gene CTNNB1 reported as other for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_001904.4(CTNNB1):c.121A>G (p.Thr41Ala) rs121913412
NM_001904.4(CTNNB1):c.133_135del (p.Ser45del) rs587776850
NM_001904.4(CTNNB1):c.134C>T (p.Ser45Phe) rs121913409
NM_001904.4(CTNNB1):c.1374A>C (p.Glu458Asp) rs1553631848
NM_001904.4(CTNNB1):c.770C>T (p.Thr257Ile) rs1553630452
NM_001904.4(CTNNB1):c.84_95del (p.Gln28_Asp32delinsHis) rs1553630102

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