"PreventionGenetics, part of Exact Sciences"[submitter] AND "CRYBB3"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3046411	NM_004076.5(CRYBB3):c.234G>A (p.Gln78=)	CRYBB3	Single nucleotide variant (synonymous variant)	CRYBB3-related disorder	GLikely benign
Select item 259228	NM_004076.5(CRYBB3):c.314G>A (p.Arg105Gln)	CRYBB3 (R105Q)	Single nucleotide variant (missense variant)	Cataract 22 multiple types +3 more	GBenign/Likely benign
Select item 259229	NM_004076.5(CRYBB3):c.337C>G (p.His113Asp)	CRYBB3 (H113D)	Single nucleotide variant (missense variant)	Cataract 22 multiple types +3 more	GBenign
Select item 3040112	NM_004076.5(CRYBB3):c.423T>C (p.Ala141=)	CRYBB3	Single nucleotide variant (synonymous variant)	CRYBB3-related disorder	GLikely benign
Select item 259230	NM_004076.5(CRYBB3):c.471-6C>T	CRYBB3	Single nucleotide variant (intron variant)	Cataract 22 multiple types +3 more	GBenign/Likely benign
Select item 466361	NM_004076.5(CRYBB3):c.547G>T (p.Glu183Ter)	CRYBB3 (E183*)	Single nucleotide variant (nonsense)	Cataract 22 multiple types +2 more	GConflicting classifications of pathogenicity

ClinVar