Related gene-specific medical variations for Gene (Select 342184) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2863286	NM_001277313.2(FMN1):c.4245T>G (p.Ser1415Arg)	FMN1, LOC126862090 (S1192R +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2803984	NM_001277313.2(FMN1):c.4216-14T>C	FMN1, LOC126862090	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2756056	NM_001277313.2(FMN1):c.4216-10dup	FMN1, LOC126862090	Duplication (intron variant)	not provided	GLikely benign
Select item 2689082	NM_001277313.2(FMN1):c.2044-1954G>A	FMN1 (G286E)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2593242	NM_001277313.2(FMN1):c.4229G>A (p.Arg1410His)	FMN1, LOC126862090 (R1187H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314910	NM_001277313.2(FMN1):c.4246G>A (p.Val1416Met)	FMN1, LOC126862090 (V1193M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1431934	NC_000015.9:g.(?_33300195)_(33300296_?)dup	FMN1	Duplication	not provided	GUncertain significance
Select item 1275341	NM_001277313.2(FMN1):c.4216-171_4216-168del	FMN1, LOC126862090	Microsatellite (intron variant)	not provided	GBenign
Select item 1267922	NM_001277313.2(FMN1):c.4216-27A>T	FMN1, LOC126862090	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238013	NM_001277313.2(FMN1):c.*33G>A	FMN1, LOC126862090	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1233503	NM_001277313.2(FMN1):c.*184C>T	FMN1, LOC126862090	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 194719	NM_001277313.2(FMN1):c.*1G>A	FMN1, LOC126862090	Single nucleotide variant (3 prime UTR variant)	not specified	GLikely benign