"PreventionGenetics, part of Exact Sciences"[submitter] AND "IRF3"[gen - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3047399	NM_001571.6(IRF3):c.1215C>T (p.Ser405=)	IRF3 (R411*)	Single nucleotide variant (nonsense +2 more)	IRF3-related disorder	GLikely benign
Select item 3039781	NM_001571.6(IRF3):c.1209C>T (p.Leu403=)	IRF3 (H409Y)	Single nucleotide variant (missense variant +2 more)	IRF3-related disorder	GBenign
Select item 2635082	NM_001571.6(IRF3):c.1066C>T (p.Gln356Ter)	IRF3 (P361L +5 more)	Single nucleotide variant (missense variant +2 more)	IRF3-related disorder	GUncertain significance
Select item 3040695	NM_001571.6(IRF3):c.885G>A (p.Val295=)	IRF3	Single nucleotide variant (synonymous variant +2 more)	IRF3-related disorder	GLikely benign
Select item 3042156	NM_001571.6(IRF3):c.834G>A (p.Gly278=)	IRF3	Single nucleotide variant (synonymous variant +2 more)	IRF3-related disorder	GLikely benign
Select item 495307	NM_001571.6(IRF3):c.829G>A (p.Ala277Thr)	IRF3 (A277T +2 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GLikely benign
Select item 3036722	NM_001571.6(IRF3):c.827G>A (p.Arg276Gln)	IRF3 (R130Q +2 more)	Single nucleotide variant (missense variant +2 more)	IRF3-related disorder	GLikely benign
Select item 3051575	NM_001571.6(IRF3):c.669G>A (p.Pro223=)	IRF3	Single nucleotide variant (synonymous variant +2 more)	IRF3-related disorder	GLikely benign
Select item 3034486	NM_001571.6(IRF3):c.523A>G (p.Ser175Gly)	IRF3 (S140G +2 more)	Single nucleotide variant (missense variant +1 more)	IRF3-related disorder	GBenign
Select item 781472	NM_001571.6(IRF3):c.432G>C (p.Leu144=)	IRF3	Single nucleotide variant (synonymous variant +2 more)	Encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 7 +2 more	GBenign/Likely benign
Select item 3055849	NM_001571.6(IRF3):c.380A>G (p.Asn127Ser)	IRF3 (N127S +1 more)	Single nucleotide variant (missense variant +2 more)	IRF3-related disorder	GLikely benign
Select item 778853	NM_001571.6(IRF3):c.287G>A (p.Arg96Gln)	IRF3 (R61Q +1 more)	Single nucleotide variant (missense variant +3 more)	IRF3-related disorder +1 more	GBenign