C4539767[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 128866	NM_001904.4(CTNNB1):c.14-4A>G	CTNNB1, LOC126806658	Single nucleotide variant (intron variant)	Medulloblastoma +7 more	GBenign/Likely benign
Select item 265443	NM_001904.4(CTNNB1):c.283C>T (p.Arg95Ter)	CTNNB1, LOC126806658 (R95* +1 more)	Single nucleotide variant (nonsense)	CTNNB1-related disorder +9 more	GPathogenic
Select item 731212	NM_001904.4(CTNNB1):c.1155C>A (p.Leu385=)	CTNNB1	Single nucleotide variant (synonymous variant)	Neoplasm of ovary +7 more	GBenign/Likely benign
Select item 39655	NM_001904.4(CTNNB1):c.1543C>T (p.Arg515Ter)	CTNNB1, LOC126806659 (R515* +1 more)	Single nucleotide variant (nonsense)	Severe intellectual disability-progressive spastic diplegia syndrome +7 more	GPathogenic
Select item 1403921	NM_001904.4(CTNNB1):c.1571A>G (p.His524Arg)	CTNNB1, LOC126806659 (H517R +1 more)	Single nucleotide variant (missense variant)	Medulloblastoma +7 more	GUncertain significance
Select item 1599823	NM_001904.4(CTNNB1):c.1683+17A>G	CTNNB1, LOC126806659	Single nucleotide variant (intron variant)	not provided +7 more	GBenign/Likely benign
Select item 210805	NM_001904.4(CTNNB1):c.2320C>T (p.Leu774=)	CTNNB1	Single nucleotide variant (synonymous variant)	not specified +8 more	GBenign/Likely benign

ClinVar