"Genome-Nilou Lab"[submitter] AND "INF2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 261603	NM_022489.4(INF2):c.105C>T (p.Pro35=)	INF2	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 261606	NM_022489.4(INF2):c.2310+8del	INF2	Deletion (intron variant)	not specified +4 more	GBenign
Select item 261611	NM_022489.4(INF2):c.2640T>C (p.Asp880=)	INF2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 261613	NM_022489.4(INF2):c.3066T>C (p.Asp1022=)	INF2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
Select item 261618	NM_022489.4(INF2):c.3207A>G (p.Pro1069=)	INF2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 261617	NM_022489.4(INF2):c.3207A>C (p.Pro1069=)	INF2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign

ClinVar