"PreventionGenetics, part of Exact Sciences"[submitter] AND "CRYBB1"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 341042	NM_001887.4(CRYBB1):c.744A>G (p.Thr248=)	CRYBA4, CRYBB1	Single nucleotide variant (synonymous variant)	CRYBB1-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 1899847	NM_001887.4(CRYBB1):c.697C>T (p.Arg233Cys)	CRYBA4, CRYBB1 (R233C)	Single nucleotide variant (missense variant)	Cataract 17 multiple types +1 more	GUncertain significance
Select item 1559028	NM_001887.4(CRYBB1):c.510C>T (p.Asp170=)	CRYBA4, CRYBB1	Single nucleotide variant (synonymous variant)	CRYBB1-related disorder +1 more	GLikely benign
Select item 901777	NM_001887.4(CRYBB1):c.294G>A (p.Ala98=)	CRYBA4, CRYBB1	Single nucleotide variant (synonymous variant)	Cataract 17 multiple types +1 more	GConflicting classifications of pathogenicity
Select item 902688	NM_001887.4(CRYBB1):c.74G>A (p.Gly25Glu)	CRYBA4, CRYBB1 (G25E)	Single nucleotide variant (missense variant)	CRYBB1-related disorder +1 more	GLikely benign
Select item 341052	NM_001887.4(CRYBB1):c.-7G>A	CRYBA4, CRYBB1	Single nucleotide variant (5 prime UTR variant)	Cataract 17 multiple types +1 more	GConflicting classifications of pathogenicity

ClinVar