"Center for Pediatric Genomic Medicine, Children's Mercy Hospital and - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 377373	NM_020066.5(FMN2):c.778G>A (p.Ala260Thr)	FMN2 (A260T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 377323	NM_020066.5(FMN2):c.953C>T (p.Pro318Leu)	FMN2 (P318L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 435219	NM_020066.5(FMN2):c.1259A>C (p.Lys420Thr)	FMN2 (K420T)	Single nucleotide variant (missense variant)	FMN2-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 445849	NM_020066.5(FMN2):c.2657T>G (p.Met886Arg)	FMN2 (M890R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 446013	NM_020066.5(FMN2):c.2844_2876del (p.Ala952_Ala962del)	FMN2	Deletion (inframe_deletion +1 more)	not provided +1 more	GBenign/Likely benign
Select item 377218	NM_020066.5(FMN2):c.2855C>G (p.Ala952Gly)	FMN2 (A956G +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 376966	NM_020066.5(FMN2):c.4123C>A (p.Leu1375Ile)	FMN2, LOC126806069 (L1379I +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance

ClinVar