"PreventionGenetics, part of Exact Sciences"[submitter] AND "CRYBA1"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3040013	NM_005208.4(CRYBA1):c.-7G>A	CRYBA1	Single nucleotide variant	CRYBA1-related condition	GBenign
Select item 259673	NM_005208.5(CRYBA1):c.74C>T (p.Pro25Leu)	CRYBA1 (P25L)	Single nucleotide variant (missense variant)	Cataract 10 multiple types +2 more	GBenign/Likely benign
Select item 1166238	NM_005208.5(CRYBA1):c.75G>A (p.Pro25=)	CRYBA1	Single nucleotide variant (synonymous variant)	Cataract 10 multiple types +1 more	GBenign/Likely benign
Select item 1571486	NM_005208.5(CRYBA1):c.173G>A (p.Arg58His)	CRYBA1 (R58H)	Single nucleotide variant (missense variant)	Cataract 10 multiple types +1 more	GLikely benign
Select item 1073011	NM_005208.5(CRYBA1):c.215+1G>C	CRYBA1	Single nucleotide variant (splice donor variant)	CRYBA1-related condition +1 more	GPathogenic
Select item 521851	NM_005208.5(CRYBA1):c.215+1G>A	CRYBA1	Single nucleotide variant (splice donor variant)	Inborn genetic diseases +3 more	GPathogenic
Select item 259671	NM_005208.5(CRYBA1):c.215+16C>T	CRYBA1	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 259672	NM_005208.5(CRYBA1):c.456C>T (p.Gly152=)	CRYBA1	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 68472	NM_005208.5(CRYBA1):c.475G>A (p.Gly159Ser)	CRYBA1 (G159S)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign/Likely benign

ClinVar