"Genome-Nilou Lab"[submitter] AND "IRF7"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1185462	NM_001572.5(IRF7):c.1357-43A>C	IRF7	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 1185463	NM_001572.5(IRF7):c.1356+32T>C	IRF7	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 1185464	NM_001572.5(IRF7):c.1237+41C>G	IRF7	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 1166881	NM_001572.5(IRF7):c.1237+14T>C	IRF7	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 1170386	NM_001572.5(IRF7):c.1235A>G (p.Gln412Arg)	IRF7 (Q383R +2 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 1170387	NM_001572.5(IRF7):c.1146A>C (p.Gly382=)	IRF7	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 1170388	NM_001572.5(IRF7):c.535A>G (p.Lys179Glu)	IRF7 (K179E +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 1170389	NM_001572.5(IRF7):c.327G>A (p.Arg109=)	IRF7	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 1170390	NM_001572.5(IRF7):c.184-3C>A	IRF7	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 1170391	NM_001572.5(IRF7):c.184-4T>A	IRF7	Single nucleotide variant (intron variant)	not specified +2 more	GBenign