"PreventionGenetics, part of Exact Sciences"[submitter] AND "IRAK3"[ge - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3035734	NM_007199.3(IRAK3):c.381+10G>A	IRAK3	Single nucleotide variant (intron variant)	IRAK3-related disorder	GLikely benign
Select item 3059815	NM_007199.3(IRAK3):c.439A>G (p.Ile147Val)	IRAK3 (I147V +1 more)	Single nucleotide variant (missense variant)	IRAK3-related disorder	GBenign
Select item 717008	NM_007199.3(IRAK3):c.468A>G (p.Gln156=)	IRAK3	Single nucleotide variant (synonymous variant)	IRAK3-related disorder +1 more	GBenign
Select item 3052038	NM_007199.3(IRAK3):c.511A>G (p.Ile171Val)	IRAK3 (I110V +1 more)	Single nucleotide variant (missense variant)	IRAK3-related disorder	GLikely benign
Select item 3053040	NM_007199.3(IRAK3):c.808A>G (p.Ile270Val)	IRAK3 (I209V +1 more)	Single nucleotide variant (missense variant)	IRAK3-related disorder	GBenign
Select item 3049609	NM_007199.3(IRAK3):c.864G>T (p.Ser288=)	IRAK3	Single nucleotide variant (synonymous variant)	IRAK3-related disorder	GLikely benign
Select item 3043733	NM_007199.3(IRAK3):c.1198C>G (p.Leu400Val)	IRAK3 (L339V +1 more)	Single nucleotide variant (missense variant)	IRAK3-related disorder	GLikely benign
Select item 3044390	NM_007199.3(IRAK3):c.1347C>T (p.Ser449=)	IRAK3	Single nucleotide variant (synonymous variant)	IRAK3-related disorder	GLikely benign
Select item 3038783	NM_007199.3(IRAK3):c.1397C>G (p.Pro466Arg)	IRAK3 (P405R +1 more)	Single nucleotide variant (missense variant)	IRAK3-related disorder	GBenign
Select item 3043454	NM_007199.3(IRAK3):c.1539G>A (p.Glu513=)	IRAK3	Single nucleotide variant (synonymous variant)	IRAK3-related disorder	GLikely benign
Select item 3039172	NM_007199.3(IRAK3):c.1653C>T (p.Ser551=)	IRAK3	Single nucleotide variant (synonymous variant)	IRAK3-related disorder	GBenign