C0206711[trait identifier] AND "Database of Curated Mutations (DoCM)"[ - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 17581	NM_001904.4(CTNNB1):c.94G>T (p.Asp32Tyr)	CTNNB1, LOC126806658 (D32Y +1 more)	Single nucleotide variant (missense variant)	Craniopharyngioma +11 more	GPathogenic/Likely pathogenic; other OOncogenic
Select item 17578	NM_001904.4(CTNNB1):c.95A>G (p.Asp32Gly)	CTNNB1, LOC126806658 (D32G +1 more)	Single nucleotide variant (missense variant)	Neoplasm of uterine cervix +10 more	GPathogenic/Likely pathogenic
Select item 17583	NM_001904.4(CTNNB1):c.98C>T (p.Ser33Phe)	CTNNB1, LOC126806658 (S33F +1 more)	Single nucleotide variant (missense variant)	Medulloblastoma +13 more	GPathogenic/Likely pathogenic; other
Select item 17577	NM_001904.4(CTNNB1):c.98C>A (p.Ser33Tyr)	CTNNB1, LOC126806658 (S33Y +1 more)	Single nucleotide variant (missense variant)	Pancreatic adenocarcinoma +13 more	GPathogenic/Likely pathogenic
Select item 376233	NM_001904.4(CTNNB1):c.100G>C (p.Gly34Arg)	CTNNB1, LOC126806658 (G34R +1 more)	Single nucleotide variant (missense variant)	Gastric adenocarcinoma +9 more	GLikely pathogenic
Select item 376232	NM_001904.4(CTNNB1):c.100G>A (p.Gly34Arg)	CTNNB1, LOC126806658 (G34R +1 more)	Single nucleotide variant (missense variant)	Pilomatrixoma +2 more	GPathogenic/Likely pathogenic
Select item 17584	NM_001904.4(CTNNB1):c.101G>A (p.Gly34Glu)	CTNNB1, LOC126806658 (G34E +1 more)	Single nucleotide variant (missense variant)	Medulloblastoma +9 more	GPathogenic/Likely pathogenic; other
Select item 17586	NM_001904.4(CTNNB1):c.110C>T (p.Ser37Phe)	CTNNB1, LOC126806658 (S37F +1 more)	Single nucleotide variant (missense variant)	Melanoma +11 more	GPathogenic/Likely pathogenic
Select item 17579	NM_001904.4(CTNNB1):c.110C>G (p.Ser37Cys)	CTNNB1, LOC126806658 (S37C +1 more)	Single nucleotide variant (missense variant)	Lung adenocarcinoma +11 more	GPathogenic/Likely pathogenic
Select item 17587	NM_001904.4(CTNNB1):c.122C>T (p.Thr41Ile)	CTNNB1, LOC126806658 (T41I +1 more)	Single nucleotide variant (missense variant)	Desmoid disease, hereditary	GLikely pathogenic