"Pathology and Clinical Laboratory Medicine, King Fahad Medical City"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 982124	NM_007293.3(C4A):c.1040C>A (p.Ser347Tyr)	C4A (S347Y)	Single nucleotide variant (no sequence alteration +2 more)	not specified	GBenign
Select item 982125	NM_007293.3(C4A):c.1045+70G>A	C4A	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 982132	NM_007293.3(C4A):c.1524+23C>A	C4A	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 982133	NM_007293.3(C4A):c.2944+55T>C	C4A	Single nucleotide variant (intron variant)	not specified +1 more	GBenign/Likely benign
Select item 982134	NM_007293.3(C4A):c.4876+50C>T	C4A	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 982135	NM_007293.3(C4A):c.5064G>A (p.Leu1688=)	C4A	Single nucleotide variant (synonymous variant)	not specified	GBenign

ClinVar